SK358591A3 - Method of production of vinylchloride polymer - Google Patents
Method of production of vinylchloride polymer Download PDFInfo
- Publication number
- SK358591A3 SK358591A3 SK3585-91A SK358591A SK358591A3 SK 358591 A3 SK358591 A3 SK 358591A3 SK 358591 A SK358591 A SK 358591A SK 358591 A3 SK358591 A3 SK 358591A3
- Authority
- SK
- Slovakia
- Prior art keywords
- poly
- polymers
- methyl
- polymerization
- vinyl
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 38
- 238000000034 method Methods 0.000 title claims abstract description 36
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 6
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 65
- 239000000178 monomer Substances 0.000 claims abstract description 47
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims abstract description 21
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 16
- 150000002391 heterocyclic compounds Chemical class 0.000 claims abstract description 12
- 150000001491 aromatic compounds Chemical class 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 9
- 239000011541 reaction mixture Substances 0.000 claims abstract description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 8
- 238000007720 emulsion polymerization reaction Methods 0.000 claims abstract description 6
- 238000010557 suspension polymerization reaction Methods 0.000 claims abstract description 5
- 239000000049 pigment Substances 0.000 claims abstract description 3
- 239000000975 dye Substances 0.000 claims abstract 2
- -1 1-aminophenentridine Chemical compound 0.000 claims description 133
- 150000001875 compounds Chemical class 0.000 claims description 56
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- 150000002484 inorganic compounds Chemical class 0.000 claims description 18
- 229910010272 inorganic material Inorganic materials 0.000 claims description 18
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 239000002184 metal Substances 0.000 claims description 17
- 230000002265 prevention Effects 0.000 claims description 13
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 5
- 150000002790 naphthalenes Chemical class 0.000 claims description 5
- 229920005615 natural polymer Polymers 0.000 claims description 5
- QWUFXJHVFNRNCU-UHFFFAOYSA-N phenazin-1-amine Chemical class C1=CC=C2N=C3C(N)=CC=CC3=NC2=C1 QWUFXJHVFNRNCU-UHFFFAOYSA-N 0.000 claims description 5
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- RHQTYDDJBYBCQV-UHFFFAOYSA-N phenazin-2-amine Chemical compound C1=CC=CC2=NC3=CC(N)=CC=C3N=C21 RHQTYDDJBYBCQV-UHFFFAOYSA-N 0.000 claims description 4
- VZPGINJWPPHRLS-UHFFFAOYSA-N phenazine-2,3-diamine Chemical compound C1=CC=C2N=C(C=C(C(N)=C3)N)C3=NC2=C1 VZPGINJWPPHRLS-UHFFFAOYSA-N 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- QWAGALBSTFENEE-UHFFFAOYSA-N 4-aminoacridine Chemical compound C1=CC=C2N=C3C(N)=CC=CC3=CC2=C1 QWAGALBSTFENEE-UHFFFAOYSA-N 0.000 claims description 3
- IUHYFLKPKSFRCT-UHFFFAOYSA-N 5-phenyl-1,3-oxazol-2-amine Chemical compound O1C(N)=NC=C1C1=CC=CC=C1 IUHYFLKPKSFRCT-UHFFFAOYSA-N 0.000 claims description 3
- LSLUWQIENURREM-UHFFFAOYSA-N 5-phenyl-1,3-thiazol-2-amine Chemical compound S1C(N)=NC=C1C1=CC=CC=C1 LSLUWQIENURREM-UHFFFAOYSA-N 0.000 claims description 3
- 229920002396 Polyurea Polymers 0.000 claims description 3
- WDVSHHCDHLJJJR-UHFFFAOYSA-N Proflavine Chemical compound C1=CC(N)=CC2=NC3=CC(N)=CC=C3C=C21 WDVSHHCDHLJJJR-UHFFFAOYSA-N 0.000 claims description 3
- LOMMDWBTANPFEJ-UHFFFAOYSA-N acridin-1-amine Chemical compound C1=CC=C2C=C3C(N)=CC=CC3=NC2=C1 LOMMDWBTANPFEJ-UHFFFAOYSA-N 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- QYOFUVIUFNSMFM-UHFFFAOYSA-N anthracene-1,4-diamine Chemical class C1=CC=C2C=C3C(N)=CC=C(N)C3=CC2=C1 QYOFUVIUFNSMFM-UHFFFAOYSA-N 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 150000001993 dienes Chemical class 0.000 claims description 3
- 229960004887 ferric hydroxide Drugs 0.000 claims description 3
- IEECXTSVVFWGSE-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Fe+3] IEECXTSVVFWGSE-UHFFFAOYSA-M 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- NTNWKDHZTDQSST-UHFFFAOYSA-N naphthalene-1,2-diamine Chemical class C1=CC=CC2=C(N)C(N)=CC=C21 NTNWKDHZTDQSST-UHFFFAOYSA-N 0.000 claims description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- 150000004760 silicates Chemical class 0.000 claims description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 3
- 235000012239 silicon dioxide Nutrition 0.000 claims description 3
- UTXPWBKKZFLMPZ-UHFFFAOYSA-N 2-aminoacridine Chemical compound C1=CC=CC2=CC3=CC(N)=CC=C3N=C21 UTXPWBKKZFLMPZ-UHFFFAOYSA-N 0.000 claims description 2
- PYSJLPAOBIGQPK-UHFFFAOYSA-N 4-phenyl-1,3-thiazol-2-amine Chemical compound S1C(N)=NC(C=2C=CC=CC=2)=C1 PYSJLPAOBIGQPK-UHFFFAOYSA-N 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 150000005022 aminoacridines Chemical class 0.000 claims description 2
- 239000000084 colloidal system Substances 0.000 claims description 2
- 229920001795 coordination polymer Polymers 0.000 claims description 2
- 229920000592 inorganic polymer Polymers 0.000 claims description 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 2
- VPRFQZSTJXHBHL-UHFFFAOYSA-N phenanthrene-9,10-diamine Chemical compound C1=CC=C2C(N)=C(N)C3=CC=CC=C3C2=C1 VPRFQZSTJXHBHL-UHFFFAOYSA-N 0.000 claims description 2
- 229920002492 poly(sulfone) Polymers 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 229920001021 polysulfide Polymers 0.000 claims description 2
- 239000005077 polysulfide Substances 0.000 claims description 2
- 150000008117 polysulfides Polymers 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 229920001959 vinylidene polymer Polymers 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- PLOCPSZUSGEEMU-UHFFFAOYSA-N phenanthridin-1-amine Chemical compound C1=CC=CC2=C3C(N)=CC=CC3=NC=C21 PLOCPSZUSGEEMU-UHFFFAOYSA-N 0.000 claims 1
- 230000003746 surface roughness Effects 0.000 claims 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 abstract description 3
- 230000003449 preventive effect Effects 0.000 abstract description 2
- 238000000576 coating method Methods 0.000 description 32
- 239000011248 coating agent Substances 0.000 description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- 239000000243 solution Substances 0.000 description 22
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 14
- 239000002253 acid Substances 0.000 description 13
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 8
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 8
- 150000002576 ketones Chemical class 0.000 description 8
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 8
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 125000005605 benzo group Chemical group 0.000 description 7
- XSCHRSMBECNVNS-UHFFFAOYSA-N benzopyrazine Natural products N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 7
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 6
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 6
- 150000004056 anthraquinones Chemical class 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 5
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 5
- 238000003556 assay Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 5
- 239000001913 cellulose Substances 0.000 description 5
- 239000008367 deionised water Substances 0.000 description 5
- 229910021641 deionized water Inorganic materials 0.000 description 5
- OKQIEBVRUGLWOR-UHFFFAOYSA-N n-naphthalen-1-ylacetamide Chemical compound C1=CC=C2C(NC(=O)C)=CC=CC2=C1 OKQIEBVRUGLWOR-UHFFFAOYSA-N 0.000 description 5
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 4
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 4
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 4
- OJVAMHKKJGICOG-UHFFFAOYSA-N 2,5-hexanedione Chemical compound CC(=O)CCC(C)=O OJVAMHKKJGICOG-UHFFFAOYSA-N 0.000 description 4
- GMTGCIAJHZEUNB-UHFFFAOYSA-N 2-pentylquinoline Chemical compound C1=CC=CC2=NC(CCCCC)=CC=C21 GMTGCIAJHZEUNB-UHFFFAOYSA-N 0.000 description 4
- MUDSDYNRBDKLGK-UHFFFAOYSA-N 4-methylquinoline Chemical compound C1=CC=C2C(C)=CC=NC2=C1 MUDSDYNRBDKLGK-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 4
- 150000001555 benzenes Chemical class 0.000 description 4
- 239000004305 biphenyl Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 4
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 229940050176 methyl chloride Drugs 0.000 description 4
- 229950000688 phenothiazine Drugs 0.000 description 4
- 229940067157 phenylhydrazine Drugs 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 4
- QVWDCTQRORVHHT-UHFFFAOYSA-N tropone Chemical compound O=C1C=CC=CC=C1 QVWDCTQRORVHHT-UHFFFAOYSA-N 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XSVWYZRKTCROSD-UHFFFAOYSA-N 2-benzhydrylnaphthalene-1,4-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 XSVWYZRKTCROSD-UHFFFAOYSA-N 0.000 description 3
- FSEXLNMNADBYJU-UHFFFAOYSA-N 2-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 3
- MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- GDALETGZDYOOGB-UHFFFAOYSA-N Acridone Natural products C1=C(O)C=C2N(C)C3=CC=CC=C3C(=O)C2=C1O GDALETGZDYOOGB-UHFFFAOYSA-N 0.000 description 3
- 229920000856 Amylose Polymers 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 108010010803 Gelatin Proteins 0.000 description 3
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 3
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Natural products CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 3
- FZEYVTFCMJSGMP-UHFFFAOYSA-N acridone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3NC2=C1 FZEYVTFCMJSGMP-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- LJOLGGXHRVADAA-UHFFFAOYSA-N benzo[e][1]benzothiole Chemical compound C1=CC=C2C(C=CS3)=C3C=CC2=C1 LJOLGGXHRVADAA-UHFFFAOYSA-N 0.000 description 3
- XHYRHAQEXJIVJX-UHFFFAOYSA-N benzo[g][1]benzothiole Chemical compound C1=CC=CC2=C(SC=C3)C3=CC=C21 XHYRHAQEXJIVJX-UHFFFAOYSA-N 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 235000011949 flavones Nutrition 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 3
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 3
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 3
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 3
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- BBNQQADTFFCFGB-UHFFFAOYSA-N purpurin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC(O)=C3C(=O)C2=C1 BBNQQADTFFCFGB-UHFFFAOYSA-N 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 3
- MAOBFOXLCJIFLV-UHFFFAOYSA-N (2-aminophenyl)-phenylmethanone Chemical class NC1=CC=CC=C1C(=O)C1=CC=CC=C1 MAOBFOXLCJIFLV-UHFFFAOYSA-N 0.000 description 2
- OKORHWXYDBSYNO-INIZCTEOSA-N (S)-codamine Chemical compound C1=C(OC)C(OC)=CC=C1C[C@H]1C2=CC(O)=C(OC)C=C2CCN1C OKORHWXYDBSYNO-INIZCTEOSA-N 0.000 description 2
- IAKHMKGGTNLKSZ-INIZCTEOSA-N (S)-colchicine Chemical compound C1([C@@H](NC(C)=O)CC2)=CC(=O)C(OC)=CC=C1C1=C2C=C(OC)C(OC)=C1OC IAKHMKGGTNLKSZ-INIZCTEOSA-N 0.000 description 2
- QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical compound C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 2
- KETQAJRQOHHATG-UHFFFAOYSA-N 1,2-naphthoquinone Chemical compound C1=CC=C2C(=O)C(=O)C=CC2=C1 KETQAJRQOHHATG-UHFFFAOYSA-N 0.000 description 2
- 229940105324 1,2-naphthoquinone Drugs 0.000 description 2
- ANLVEXKNRYNLDH-UHFFFAOYSA-N 1,3-dioxonan-2-one Chemical compound O=C1OCCCCCCO1 ANLVEXKNRYNLDH-UHFFFAOYSA-N 0.000 description 2
- APQSQLNWAIULLK-UHFFFAOYSA-N 1,4-dimethylnaphthalene Chemical compound C1=CC=C2C(C)=CC=C(C)C2=C1 APQSQLNWAIULLK-UHFFFAOYSA-N 0.000 description 2
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 2
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 2
- SDDBCEWUYXVGCQ-UHFFFAOYSA-N 1,5-dimethylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1C SDDBCEWUYXVGCQ-UHFFFAOYSA-N 0.000 description 2
- CBMXCNPQDUJNHT-UHFFFAOYSA-N 1,6-dimethylnaphthalene Chemical compound CC1=CC=CC2=CC(C)=CC=C21 CBMXCNPQDUJNHT-UHFFFAOYSA-N 0.000 description 2
- NJJDXYXIDPRRDB-UHFFFAOYSA-N 1-[chloro(phenyl)methyl]naphthalene Chemical compound C=1C=CC2=CC=CC=C2C=1C(Cl)C1=CC=CC=C1 NJJDXYXIDPRRDB-UHFFFAOYSA-N 0.000 description 2
- GESUXCLRERRNSQ-UHFFFAOYSA-N 1-benzhydrylnaphthalene Chemical compound C1=CC=CC=C1C(C=1C2=CC=CC=C2C=CC=1)C1=CC=CC=C1 GESUXCLRERRNSQ-UHFFFAOYSA-N 0.000 description 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- AZFWKWBXGOGJOI-UHFFFAOYSA-N 1-chloro-4-(chloromethyl)naphthalene Chemical compound C1=CC=C2C(CCl)=CC=C(Cl)C2=C1 AZFWKWBXGOGJOI-UHFFFAOYSA-N 0.000 description 2
- ZYDGCYWJDWIJCS-UHFFFAOYSA-N 1-methoxyphenazine Chemical compound C1=CC=C2N=C3C(OC)=CC=CC3=NC2=C1 ZYDGCYWJDWIJCS-UHFFFAOYSA-N 0.000 description 2
- PBYMYAJONQZORL-UHFFFAOYSA-N 1-methylisoquinoline Chemical compound C1=CC=C2C(C)=NC=CC2=C1 PBYMYAJONQZORL-UHFFFAOYSA-N 0.000 description 2
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- DOWJXOHBNXRUOD-UHFFFAOYSA-N 1-methylphenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1C(C)=CC=C2 DOWJXOHBNXRUOD-UHFFFAOYSA-N 0.000 description 2
- IYDMICQAKLQHLA-UHFFFAOYSA-N 1-phenylnaphthalene Chemical class C1=CC=CC=C1C1=CC=CC2=CC=CC=C12 IYDMICQAKLQHLA-UHFFFAOYSA-N 0.000 description 2
- PMPBFICDXLLSRM-UHFFFAOYSA-N 1-propan-2-ylnaphthalene Chemical compound C1=CC=C2C(C(C)C)=CC=CC2=C1 PMPBFICDXLLSRM-UHFFFAOYSA-N 0.000 description 2
- ZMFJCQAPRNRDSK-UHFFFAOYSA-N 10-oxidophenazin-5-ium 5-oxide Chemical compound C1=CC=C2N([O-])C3=CC=CC=C3[N+](=O)C2=C1 ZMFJCQAPRNRDSK-UHFFFAOYSA-N 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
- HTQYGVOVAUJXMF-UHFFFAOYSA-N 2,3-dianilinonaphthalene-1,4-dione Chemical compound C=1C=CC=CC=1NC=1C(=O)C2=CC=CC=C2C(=O)C=1NC1=CC=CC=C1 HTQYGVOVAUJXMF-UHFFFAOYSA-N 0.000 description 2
- VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 description 2
- WWGUMAYGTYQSGA-UHFFFAOYSA-N 2,3-dimethylnaphthalene Chemical compound C1=CC=C2C=C(C)C(C)=CC2=C1 WWGUMAYGTYQSGA-UHFFFAOYSA-N 0.000 description 2
- VDYFFXPVIBDLOT-UHFFFAOYSA-N 2,4-dimethylquinazoline Chemical compound C1=CC=CC2=NC(C)=NC(C)=C21 VDYFFXPVIBDLOT-UHFFFAOYSA-N 0.000 description 2
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 2
- YGYNBBAUIYTWBF-UHFFFAOYSA-N 2,6-dimethylnaphthalene Chemical compound C1=C(C)C=CC2=CC(C)=CC=C21 YGYNBBAUIYTWBF-UHFFFAOYSA-N 0.000 description 2
- LRQYSMQNJLZKPS-UHFFFAOYSA-N 2,7-dimethylnaphthalene Chemical compound C1=CC(C)=CC2=CC(C)=CC=C21 LRQYSMQNJLZKPS-UHFFFAOYSA-N 0.000 description 2
- DHMPJEGFPQTNFX-UHFFFAOYSA-N 2-(2,5-dihydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-3,6-dihydroxy-5-methylcyclohexa-2,5-diene-1,4-dione Chemical compound O=C1C(C)=C(O)C(=O)C(C=2C(C(O)=C(C)C(=O)C=2O)=O)=C1O DHMPJEGFPQTNFX-UHFFFAOYSA-N 0.000 description 2
- RETSEGNZNUBJRB-UHFFFAOYSA-N 2-Hydroxyphenazine Chemical compound C1=CC=CC2=NC3=CC(O)=CC=C3N=C21 RETSEGNZNUBJRB-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- ZYHQGITXIJDDKC-UHFFFAOYSA-N 2-[2-(2-aminophenyl)ethyl]aniline Chemical group NC1=CC=CC=C1CCC1=CC=CC=C1N ZYHQGITXIJDDKC-UHFFFAOYSA-N 0.000 description 2
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 2
- OPECBHGHSFBITB-UHFFFAOYSA-N 2-anilinonaphthalene-1,4-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C=C1NC1=CC=CC=C1 OPECBHGHSFBITB-UHFFFAOYSA-N 0.000 description 2
- XFNILMZFMFGHFM-UHFFFAOYSA-N 2-benzhydryl-3-methylnaphthalene-1,4-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C(C)=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 XFNILMZFMFGHFM-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- RJTJVVYSTUQWNI-UHFFFAOYSA-N 2-ethylnaphthalene Chemical compound C1=CC=CC2=CC(CC)=CC=C21 RJTJVVYSTUQWNI-UHFFFAOYSA-N 0.000 description 2
- QIMMUPPBPVKWKM-UHFFFAOYSA-N 2-methylnaphthalene Chemical compound C1=CC=CC2=CC(C)=CC=C21 QIMMUPPBPVKWKM-UHFFFAOYSA-N 0.000 description 2
- ALHUXMDEZNLFTA-UHFFFAOYSA-N 2-methylquinoxaline Chemical compound C1=CC=CC2=NC(C)=CN=C21 ALHUXMDEZNLFTA-UHFFFAOYSA-N 0.000 description 2
- KLLLJCACIRKBDT-UHFFFAOYSA-N 2-phenyl-1H-indole Chemical compound N1C2=CC=CC=C2C=C1C1=CC=CC=C1 KLLLJCACIRKBDT-UHFFFAOYSA-N 0.000 description 2
- IRTLROCMFSDSNF-UHFFFAOYSA-N 2-phenyl-1h-pyrrole Chemical compound C1=CNC(C=2C=CC=CC=2)=C1 IRTLROCMFSDSNF-UHFFFAOYSA-N 0.000 description 2
- TURIHPLQSRVWHU-UHFFFAOYSA-N 2-phenylnaphthalene Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=C1 TURIHPLQSRVWHU-UHFFFAOYSA-N 0.000 description 2
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 2
- TVYVQNHYIHAJTD-UHFFFAOYSA-N 2-propan-2-ylnaphthalene Chemical compound C1=CC=CC2=CC(C(C)C)=CC=C21 TVYVQNHYIHAJTD-UHFFFAOYSA-N 0.000 description 2
- WUBNJKMFYXGQDB-UHFFFAOYSA-N 3,3-diphenyl-2-benzofuran-1-one Chemical compound C12=CC=CC=C2C(=O)OC1(C=1C=CC=CC=1)C1=CC=CC=C1 WUBNJKMFYXGQDB-UHFFFAOYSA-N 0.000 description 2
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 description 2
- DTBDAFLSBDGPEA-UHFFFAOYSA-N 3-methylquinoline Chemical compound C1=CC=CC2=CC(C)=CN=C21 DTBDAFLSBDGPEA-UHFFFAOYSA-N 0.000 description 2
- OKRIMXDIYQGPBU-UHFFFAOYSA-N 3-nitroso-2-phenyl-1h-indole Chemical compound N1C2=CC=CC=C2C(N=O)=C1C1=CC=CC=C1 OKRIMXDIYQGPBU-UHFFFAOYSA-N 0.000 description 2
- ZPKRDBXIPFYPTF-UHFFFAOYSA-N 3-phenylquinoline Chemical compound C1=CC=CC=C1C1=CN=C(C=CC=C2)C2=C1 ZPKRDBXIPFYPTF-UHFFFAOYSA-N 0.000 description 2
- DATYUTWESAKQQM-UHFFFAOYSA-N 4,7-phenanthroline Chemical compound C1=CC=C2C3=CC=CN=C3C=CC2=N1 DATYUTWESAKQQM-UHFFFAOYSA-N 0.000 description 2
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
- GBEBHUXJNVPKMN-UHFFFAOYSA-N 4-methoxy-2-pentylquinoline Chemical compound C1=CC=CC2=NC(CCCCC)=CC(OC)=C21 GBEBHUXJNVPKMN-UHFFFAOYSA-N 0.000 description 2
- CVJHRDUVYHASOG-UHFFFAOYSA-N 4-methoxy-2-phenylquinoline Chemical compound N=1C2=CC=CC=C2C(OC)=CC=1C1=CC=CC=C1 CVJHRDUVYHASOG-UHFFFAOYSA-N 0.000 description 2
- UCZJPQIEFFTIEV-UHFFFAOYSA-N 5-methoxy-6-methyl-2-phenylchromen-7-one Chemical compound C=1C=C2C(OC)=C(C)C(=O)C=C2OC=1C1=CC=CC=C1 UCZJPQIEFFTIEV-UHFFFAOYSA-N 0.000 description 2
- BGEBZHIAGXMEMV-UHFFFAOYSA-N 5-methoxypsoralen Chemical compound O1C(=O)C=CC2=C1C=C1OC=CC1=C2OC BGEBZHIAGXMEMV-UHFFFAOYSA-N 0.000 description 2
- FFISWZPYNKWIRR-UHFFFAOYSA-N 5-oxidophenazin-5-ium Chemical compound C1=CC=C2[N+]([O-])=C(C=CC=C3)C3=NC2=C1 FFISWZPYNKWIRR-UHFFFAOYSA-N 0.000 description 2
- ZLLOWHFKKIOINR-UHFFFAOYSA-N 5-phenyl-1,3-thiazole Chemical compound S1C=NC=C1C1=CC=CC=C1 ZLLOWHFKKIOINR-UHFFFAOYSA-N 0.000 description 2
- PWSZRRFDVPMZGM-UHFFFAOYSA-N 5-phenyl-1h-pyrazol-3-amine Chemical compound N1N=C(N)C=C1C1=CC=CC=C1 PWSZRRFDVPMZGM-UHFFFAOYSA-N 0.000 description 2
- OEDUIFSDODUDRK-UHFFFAOYSA-N 5-phenyl-1h-pyrazole Chemical compound N1N=CC=C1C1=CC=CC=C1 OEDUIFSDODUDRK-UHFFFAOYSA-N 0.000 description 2
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 2
- LUYISICIYVKBTA-UHFFFAOYSA-N 6-methylquinoline Chemical compound N1=CC=CC2=CC(C)=CC=C21 LUYISICIYVKBTA-UHFFFAOYSA-N 0.000 description 2
- KDJVHSVOXOZBDR-UHFFFAOYSA-N 8-(2-hydroxypropan-2-yl)furo[2,3-h]chromen-2-one Chemical compound C1=CC(=O)OC2=C1C=CC1=C2C=C(C(C)(O)C)O1 KDJVHSVOXOZBDR-UHFFFAOYSA-N 0.000 description 2
- XXPBFNVKTVJZKF-UHFFFAOYSA-N 9,10-dihydrophenanthrene Chemical compound C1=CC=C2CCC3=CC=CC=C3C2=C1 XXPBFNVKTVJZKF-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 2
- FMMWHPNWAFZXNH-UHFFFAOYSA-N Benz[a]pyrene Chemical compound C1=C2C3=CC=CC=C3C=C(C=C3)C2=C2C3=CC=CC2=C1 FMMWHPNWAFZXNH-UHFFFAOYSA-N 0.000 description 2
- BPYKTIZUTYGOLE-IFADSCNNSA-N Bilirubin Chemical compound N1C(=O)C(C)=C(C=C)\C1=C\C1=C(C)C(CCC(O)=O)=C(CC2=C(C(C)=C(\C=C/3C(=C(C=C)C(=O)N\3)C)N2)CCC(O)=O)N1 BPYKTIZUTYGOLE-IFADSCNNSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- DPXXJCMMMXZVSW-UHFFFAOYSA-N Casimiroin Chemical compound C1=C2C(OC)=CC(=O)N(C)C2=C2OCOC2=C1 DPXXJCMMMXZVSW-UHFFFAOYSA-N 0.000 description 2
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- WIONIXOBNMDJFJ-UHFFFAOYSA-N Dictamnine Chemical compound C1=CC=C2C(OC)=C(C=CO3)C3=NC2=C1 WIONIXOBNMDJFJ-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- UEXCJVNBTNXOEH-UHFFFAOYSA-N Ethynylbenzene Chemical group C#CC1=CC=CC=C1 UEXCJVNBTNXOEH-UHFFFAOYSA-N 0.000 description 2
- IMJCEVWDXKCHOI-UHFFFAOYSA-N Flindersiamine Chemical compound N1=C2C(OC)=C(OCO3)C3=CC2=C(OC)C2=C1OC=C2 IMJCEVWDXKCHOI-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 2
- XNWPXDGRBWJIES-UHFFFAOYSA-N Maclurin Chemical compound OC1=CC(O)=CC(O)=C1C(=O)C1=CC=C(O)C(O)=C1 XNWPXDGRBWJIES-UHFFFAOYSA-N 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- URPVDDXMEZAEJY-UHFFFAOYSA-N Melicopicine Natural products C1=CC=C2C(=O)C3=C(OC)C(OC)=C(OC)C(OC)=C3N(C)C2=C1 URPVDDXMEZAEJY-UHFFFAOYSA-N 0.000 description 2
- TZZNUDMEMFBPQI-UHFFFAOYSA-N Melicopidine Chemical compound CN1C2=CC=CC=C2C(=O)C2=C1C(OC)=C(OCO1)C1=C2OC TZZNUDMEMFBPQI-UHFFFAOYSA-N 0.000 description 2
- MJVAVZPDRWSRRC-UHFFFAOYSA-N Menadione Chemical compound C1=CC=C2C(=O)C(C)=CC(=O)C2=C1 MJVAVZPDRWSRRC-UHFFFAOYSA-N 0.000 description 2
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 2
- LMGZCSKYOKDBES-AEFFLSMTSA-N Narcotoline Chemical compound CN1CCC2=CC=3OCOC=3C(O)=C2[C@@H]1[C@@H]1C2=CC=C(OC)C(OC)=C2C(=O)O1 LMGZCSKYOKDBES-AEFFLSMTSA-N 0.000 description 2
- LMGZCSKYOKDBES-WMZOPIPTSA-N Narcotoline Natural products O(C)c1c(OC)ccc2[C@@H]([C@H]3N(C)CCc4c3c(O)c3OCOc3c4)OC(=O)c12 LMGZCSKYOKDBES-WMZOPIPTSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 102000035028 Nucleic proteins Human genes 0.000 description 2
- 108091005461 Nucleic proteins Proteins 0.000 description 2
- QJTBIAMBPGGIGI-UHFFFAOYSA-N Papaveraldine Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)C1=NC=CC2=CC(OC)=C(OC)C=C12 QJTBIAMBPGGIGI-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 2
- QUVCQYQEIOLHFZ-UHFFFAOYSA-N Seselin Chemical compound C1=CC(=O)OC2=C(C=CC(C)(C)O3)C3=CC=C21 QUVCQYQEIOLHFZ-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- GAMYVSCDDLXAQW-AOIWZFSPSA-N Thermopsosid Natural products O(C)c1c(O)ccc(C=2Oc3c(c(O)cc(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O4)c3)C(=O)C=2)c1 GAMYVSCDDLXAQW-AOIWZFSPSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- DWFDGERFICTFQW-UHFFFAOYSA-N [1,3]dioxolo[4,5-g]isoquinoline Chemical compound C1=NC=C2C=C(OCO3)C3=CC2=C1 DWFDGERFICTFQW-UHFFFAOYSA-N 0.000 description 2
- RJLFUNFLEVXGOV-UHFFFAOYSA-N [Si]([O-])(O)(O)O[Si](O)(O)O.[Si](O)(O)(O)O[Si](O)(O)O.[K+] Chemical compound [Si]([O-])(O)(O)O[Si](O)(O)O.[Si](O)(O)(O)O[Si](O)(O)O.[K+] RJLFUNFLEVXGOV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229930013930 alkaloid Natural products 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 2
- HCAUQPZEWLULFJ-UHFFFAOYSA-N benzo[f]quinoline Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=N1 HCAUQPZEWLULFJ-UHFFFAOYSA-N 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- GIJHDGJRTUSBJR-UHFFFAOYSA-N bergaptol Chemical compound O1C(=O)C=CC2=C1C=C1OC=CC1=C2O GIJHDGJRTUSBJR-UHFFFAOYSA-N 0.000 description 2
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- VQFAIAKCILWQPZ-UHFFFAOYSA-N bromoacetone Chemical compound CC(=O)CBr VQFAIAKCILWQPZ-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- 125000005606 carbostyryl group Chemical group 0.000 description 2
- 239000005018 casein Substances 0.000 description 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
- 235000021240 caseins Nutrition 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- STLZCUYBVPNYED-UHFFFAOYSA-N chlorbetamide Chemical compound OCCN(C(=O)C(Cl)Cl)CC1=CC=C(Cl)C=C1Cl STLZCUYBVPNYED-UHFFFAOYSA-N 0.000 description 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 2
- ZPEIMTDSQAKGNT-UHFFFAOYSA-N chlorpromazine Chemical compound C1=C(Cl)C=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 ZPEIMTDSQAKGNT-UHFFFAOYSA-N 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- QBPFLULOKWLNNW-UHFFFAOYSA-N chrysazin Chemical compound O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=CC=C2O QBPFLULOKWLNNW-UHFFFAOYSA-N 0.000 description 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 2
- KMPWYEUPVWOPIM-UHFFFAOYSA-N cinchonidine Natural products C1=CC=C2C(C(C3N4CCC(C(C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-UHFFFAOYSA-N 0.000 description 2
- KMPWYEUPVWOPIM-LSOMNZGLSA-N cinchonine Chemical compound C1=CC=C2C([C@@H]([C@H]3N4CC[C@H]([C@H](C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-LSOMNZGLSA-N 0.000 description 2
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- VPUGDVKSAQVFFS-UHFFFAOYSA-N coronene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3)C4=C4C3=CC=C(C=C3)C4=C2C3=C1 VPUGDVKSAQVFFS-UHFFFAOYSA-N 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- YKROEKFLSMDUSV-UHFFFAOYSA-N dipyridin-3-yldiazene Chemical compound C1=CN=CC(N=NC=2C=NC=CC=2)=C1 YKROEKFLSMDUSV-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 2
- VOLZBKQSLGCZGC-UHFFFAOYSA-N egonol Chemical compound C1=C2OCOC2=CC(C2=CC=3C=C(CCCO)C=C(C=3O2)OC)=C1 VOLZBKQSLGCZGC-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229930003944 flavone Natural products 0.000 description 2
- 150000007946 flavonol Chemical class 0.000 description 2
- HVQAJTFOCKOKIN-UHFFFAOYSA-N flavonol Natural products O1C2=CC=CC=C2C(=O)C(O)=C1C1=CC=CC=C1 HVQAJTFOCKOKIN-UHFFFAOYSA-N 0.000 description 2
- 235000011957 flavonols Nutrition 0.000 description 2
- JKFAIQOWCVVSKC-UHFFFAOYSA-N furazan Chemical compound C=1C=NON=1 JKFAIQOWCVVSKC-UHFFFAOYSA-N 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 2
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 description 2
- MPYHGNAJOKCMAQ-UHFFFAOYSA-N laudanine Chemical compound C1=C(O)C(OC)=CC=C1CC1C2=CC(OC)=C(OC)C=C2CCN1C MPYHGNAJOKCMAQ-UHFFFAOYSA-N 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 2
- 229960000907 methylthioninium chloride Drugs 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- AJPOUQFCBFQUNH-UHFFFAOYSA-N n-ethyl-n-methylnaphthalen-1-amine Chemical compound C1=CC=C2C(N(C)CC)=CC=CC2=C1 AJPOUQFCBFQUNH-UHFFFAOYSA-N 0.000 description 2
- CXAYOCVHDCXPAI-UHFFFAOYSA-N naphthalen-1-yl(phenyl)methanone Chemical class C=1C=CC2=CC=CC=C2C=1C(=O)C1=CC=CC=C1 CXAYOCVHDCXPAI-UHFFFAOYSA-N 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 2
- XQYZDYMELSJDRZ-UHFFFAOYSA-N papaverine Chemical compound C1=C(OC)C(OC)=CC=C1CC1=NC=CC2=CC(OC)=C(OC)C=C12 XQYZDYMELSJDRZ-UHFFFAOYSA-N 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 2
- YQBNJPACAUPNLV-UHFFFAOYSA-N peucedanin Chemical compound O1C(=O)C=CC2=C1C=C1OC(C(C)C)=C(OC)C1=C2 YQBNJPACAUPNLV-UHFFFAOYSA-N 0.000 description 2
- CXZOCEZMGWOOFD-UHFFFAOYSA-N phenanthren-1-amine Chemical compound C1=CC2=CC=CC=C2C2=C1C(N)=CC=C2 CXZOCEZMGWOOFD-UHFFFAOYSA-N 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- GBROPGWFBFCKAG-UHFFFAOYSA-N picene Chemical compound C1=CC2=C3C=CC=CC3=CC=C2C2=C1C1=CC=CC=C1C=C2 GBROPGWFBFCKAG-UHFFFAOYSA-N 0.000 description 2
- 239000004584 polyacrylic acid Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 description 2
- GUEIZVNYDFNHJU-UHFFFAOYSA-N quinizarin Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2O GUEIZVNYDFNHJU-UHFFFAOYSA-N 0.000 description 2
- 150000004053 quinones Chemical class 0.000 description 2
- NXLOLUFNDSBYTP-UHFFFAOYSA-N retene Chemical compound C1=CC=C2C3=CC=C(C(C)C)C=C3C=CC2=C1C NXLOLUFNDSBYTP-UHFFFAOYSA-N 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229940035044 sorbitan monolaurate Drugs 0.000 description 2
- 241000894007 species Species 0.000 description 2
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 2
- 235000021286 stilbenes Nutrition 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- GTQXMAIXVFLYKF-UHFFFAOYSA-N thiochrome Chemical compound CC1=NC=C2CN3C(C)=C(CCO)SC3=NC2=N1 GTQXMAIXVFLYKF-UHFFFAOYSA-N 0.000 description 2
- 229930192474 thiophene Natural products 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- SLGBZMMZGDRARJ-UHFFFAOYSA-N triphenylene Chemical compound C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C2=C1 SLGBZMMZGDRARJ-UHFFFAOYSA-N 0.000 description 2
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 2
- DNXHEGUUPJUMQT-UHFFFAOYSA-N (+)-estrone Natural products OC1=CC=C2C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 DNXHEGUUPJUMQT-UHFFFAOYSA-N 0.000 description 1
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
- DEEUSUJLZQQESV-BQUSTMGCSA-N (-)-stercobilin Chemical compound N1C(=O)[C@H](C)[C@@H](CC)[C@@H]1CC1=C(C)C(CCC(O)=O)=C(\C=C/2C(=C(C)C(C[C@H]3[C@@H]([C@@H](CC)C(=O)N3)C)=N\2)CCC(O)=O)N1 DEEUSUJLZQQESV-BQUSTMGCSA-N 0.000 description 1
- COWSLJWFSRYRBO-UHFFFAOYSA-N (1,5-diphenylpyrazol-4-yl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C=1C=NN(C=2C=CC=CC=2)C=1C1=CC=CC=C1 COWSLJWFSRYRBO-UHFFFAOYSA-N 0.000 description 1
- AOVGTXWIQWMZGB-YUMQZZPRSA-N (1r,2r)-cyclohexane-1,2-dicarbaldehyde Chemical compound O=C[C@@H]1CCCC[C@H]1C=O AOVGTXWIQWMZGB-YUMQZZPRSA-N 0.000 description 1
- WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
- GRDGBWVSVMLKBV-UHFFFAOYSA-N (2-amino-5-nitrophenyl)-(2-chlorophenyl)methanone Chemical compound NC1=CC=C([N+]([O-])=O)C=C1C(=O)C1=CC=CC=C1Cl GRDGBWVSVMLKBV-UHFFFAOYSA-N 0.000 description 1
- CDRBCCBXXHTNSU-UHFFFAOYSA-N (2-aminophenyl)-naphthalen-1-ylmethanone Chemical compound NC1=CC=CC=C1C(=O)C1=CC=CC2=CC=CC=C12 CDRBCCBXXHTNSU-UHFFFAOYSA-N 0.000 description 1
- LRGQYUQVMIAJOQ-UHFFFAOYSA-N (2-methyl-1H-indol-3-yl)-phenyldiazene Chemical compound Cc1[nH]c2ccccc2c1N=Nc1ccccc1 LRGQYUQVMIAJOQ-UHFFFAOYSA-N 0.000 description 1
- KPGIOJKKLPOAGL-UHFFFAOYSA-N (2-methylphenyl)-naphthalen-1-ylmethanone Chemical compound CC1=CC=CC=C1C(=O)C1=CC=CC2=CC=CC=C12 KPGIOJKKLPOAGL-UHFFFAOYSA-N 0.000 description 1
- YBCHHYHHCROEGT-UHFFFAOYSA-N (2-methylquinolin-8-yl)-phenylmethanone Chemical compound C12=NC(C)=CC=C2C=CC=C1C(=O)C1=CC=CC=C1 YBCHHYHHCROEGT-UHFFFAOYSA-N 0.000 description 1
- UJHSIDUUJPTLDY-UHFFFAOYSA-N (2-nitrophenyl)-phenylmethanone Chemical compound [O-][N+](=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 UJHSIDUUJPTLDY-UHFFFAOYSA-N 0.000 description 1
- AFDGHQDYRGPFDJ-UHFFFAOYSA-N (3,4-diphenyl-1,2-oxazol-5-yl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C=1ON=C(C=2C=CC=CC=2)C=1C1=CC=CC=C1 AFDGHQDYRGPFDJ-UHFFFAOYSA-N 0.000 description 1
- MFYLRNKOXORIPK-UHFFFAOYSA-N (3-nitrophenyl)-phenylmethanone Chemical compound [O-][N+](=O)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 MFYLRNKOXORIPK-UHFFFAOYSA-N 0.000 description 1
- GUNLFCZMCDYCMU-AATRIKPKSA-N (3e)-1,6-dioxacyclododec-3-ene-2,5-dione Chemical compound O=C/1OCCCCCCOC(=O)\C=C\1 GUNLFCZMCDYCMU-AATRIKPKSA-N 0.000 description 1
- GUNLFCZMCDYCMU-WAYWQWQTSA-N (3z)-1,6-dioxacyclododec-3-ene-2,5-dione Chemical compound O=C\1OCCCCCCOC(=O)\C=C/1 GUNLFCZMCDYCMU-WAYWQWQTSA-N 0.000 description 1
- YOAYTFFJHPBDIJ-UHFFFAOYSA-N (4,4-dichlorocyclohexa-1,5-dien-1-yl)-phenyldiazene Chemical compound ClC1(CC=C(C=C1)N=NC1=CC=CC=C1)Cl YOAYTFFJHPBDIJ-UHFFFAOYSA-N 0.000 description 1
- IAXXETNIOYFMLW-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) 2-methylprop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C(=C)C)CC1C2(C)C IAXXETNIOYFMLW-UHFFFAOYSA-N 0.000 description 1
- DKSJRIWNWIRVCV-UHFFFAOYSA-N (4-benzoylnaphthalen-1-yl)-phenylmethanone Chemical compound C=1C=C(C(=O)C=2C=CC=CC=2)C2=CC=CC=C2C=1C(=O)C1=CC=CC=C1 DKSJRIWNWIRVCV-UHFFFAOYSA-N 0.000 description 1
- NPENBPVOAXERED-UHFFFAOYSA-N (4-benzoylphenyl)-phenylmethanone Chemical compound C=1C=C(C(=O)C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 NPENBPVOAXERED-UHFFFAOYSA-N 0.000 description 1
- SVJSEJOASMWXGQ-UHFFFAOYSA-N (4-bromophenyl)-phenyldiazene Chemical compound C1=CC(Br)=CC=C1N=NC1=CC=CC=C1 SVJSEJOASMWXGQ-UHFFFAOYSA-N 0.000 description 1
- QWMJEUJXWVZSAG-UHFFFAOYSA-N (4-ethenylphenyl)boronic acid Chemical compound OB(O)C1=CC=C(C=C)C=C1 QWMJEUJXWVZSAG-UHFFFAOYSA-N 0.000 description 1
- VANIRKXGZSRTMW-UHFFFAOYSA-N (4-hydroxynaphthalen-1-yl)-phenylmethanone Chemical compound C12=CC=CC=C2C(O)=CC=C1C(=O)C1=CC=CC=C1 VANIRKXGZSRTMW-UHFFFAOYSA-N 0.000 description 1
- WXPWZZHELZEVPO-UHFFFAOYSA-N (4-methylphenyl)-phenylmethanone Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=CC=C1 WXPWZZHELZEVPO-UHFFFAOYSA-N 0.000 description 1
- TZTDJBMGPQLSLI-UHFFFAOYSA-N (4-nitrophenyl)-phenyldiazene Chemical compound C1=CC([N+](=O)[O-])=CC=C1N=NC1=CC=CC=C1 TZTDJBMGPQLSLI-UHFFFAOYSA-N 0.000 description 1
- DHPRQBPJLMKORJ-XRNKAMNCSA-N (4s,4as,5as,6s,12ar)-7-chloro-4-(dimethylamino)-1,6,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide Chemical compound C1=CC(Cl)=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]4(O)C(=O)C3=C(O)C2=C1O DHPRQBPJLMKORJ-XRNKAMNCSA-N 0.000 description 1
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- RGWIUVQFCJSWAB-UHFFFAOYSA-N (5-benzoyl-2,4-dimethylphenyl)-phenylmethanone Chemical compound CC1=CC(C)=C(C(=O)C=2C=CC=CC=2)C=C1C(=O)C1=CC=CC=C1 RGWIUVQFCJSWAB-UHFFFAOYSA-N 0.000 description 1
- IYGYMKDQCDOMRE-ROUUACIJSA-N (6s)-6-[(5s)-6-methyl-7,8-dihydro-5h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]-6h-furo[3,4-g][1,3]benzodioxol-8-one Chemical compound O([C@@H]1[C@@H]2C3=CC=4OCOC=4C=C3CCN2C)C(=O)C2=C1C=CC1=C2OCO1 IYGYMKDQCDOMRE-ROUUACIJSA-N 0.000 description 1
- HSDSUBIABLFGDX-AWEZNQCLSA-N (7s)-7-amino-1,2,3-trimethoxy-6,7-dihydro-5h-dibenzo[5,3-b:1',2'-e][7]annulen-9-ol Chemical compound C1C[C@H](N)C2=CC(O)=CC=C2C2=C1C=C(OC)C(OC)=C2OC HSDSUBIABLFGDX-AWEZNQCLSA-N 0.000 description 1
- LYFPBWOBIJJASK-INIZCTEOSA-N (S)-(-)-Canadine Natural products O(C)c1c(OC)ccc2c1C[N+]1[C@H](c3c(cc4OCOc4c3)CC1)C2 LYFPBWOBIJJASK-INIZCTEOSA-N 0.000 description 1
- LVVKXRQZSRUVPY-HNNXBMFYSA-N (S)-coclaurine Chemical compound C([C@@H]1NCCC=2C=C(C(=CC=21)O)OC)C1=CC=C(O)C=C1 LVVKXRQZSRUVPY-HNNXBMFYSA-N 0.000 description 1
- SDJKQYUTPDOVQI-JLHYYAGUSA-N (e)-1-(1-hydroxynaphthalen-2-yl)-3-phenylprop-2-en-1-one Chemical compound C1=CC2=CC=CC=C2C(O)=C1C(=O)\C=C\C1=CC=CC=C1 SDJKQYUTPDOVQI-JLHYYAGUSA-N 0.000 description 1
- RSYVUCWGXLBPOV-BUHFOSPRSA-N (e)-1-naphthalen-1-yl-3-phenylprop-2-en-1-one Chemical compound C=1C=CC2=CC=CC=C2C=1C(=O)\C=C\C1=CC=CC=C1 RSYVUCWGXLBPOV-BUHFOSPRSA-N 0.000 description 1
- DMDPKUWXJUYFKO-UHFFFAOYSA-N 1,1'-biphenyl;hydrochloride Chemical compound Cl.C1=CC=CC=C1C1=CC=CC=C1 DMDPKUWXJUYFKO-UHFFFAOYSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical group FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 description 1
- GJKIRZMMCLLZOJ-UHFFFAOYSA-N 1,1-dichloro-2h-naphthalene Chemical compound C1=CC=C2C(Cl)(Cl)CC=CC2=C1 GJKIRZMMCLLZOJ-UHFFFAOYSA-N 0.000 description 1
- DUSTWKRUAGOEKK-UHFFFAOYSA-N 1,1-dinaphthalen-1-ylurea Chemical compound C1=CC=C2C(N(C=3C4=CC=CC=C4C=CC=3)C(=O)N)=CC=CC2=C1 DUSTWKRUAGOEKK-UHFFFAOYSA-N 0.000 description 1
- YPYBVYAVVFLHDN-UHFFFAOYSA-N 1,10-phenanthrolin-2-amine Chemical compound C1=CN=C2C3=NC(N)=CC=C3C=CC2=C1 YPYBVYAVVFLHDN-UHFFFAOYSA-N 0.000 description 1
- AKLNFWFRTNMKKG-UHFFFAOYSA-N 1,12-dioxacyclooctacosane-2,11-dione Chemical compound O=C1CCCCCCCCC(=O)OCCCCCCCCCCCCCCCCO1 AKLNFWFRTNMKKG-UHFFFAOYSA-N 0.000 description 1
- JRZKNHITLINYHV-UHFFFAOYSA-N 1,2,3,4,5-pentachloronaphthalene Chemical compound ClC1=CC=CC2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21 JRZKNHITLINYHV-UHFFFAOYSA-N 0.000 description 1
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
- GGOFJXABVRZLJH-UHFFFAOYSA-N 1,2,3,4-tetrachloroanthracene Chemical compound C1=CC=CC2=CC3=C(Cl)C(Cl)=C(Cl)C(Cl)=C3C=C21 GGOFJXABVRZLJH-UHFFFAOYSA-N 0.000 description 1
- NAQWICRLNQSPPW-UHFFFAOYSA-N 1,2,3,4-tetrachloronaphthalene Chemical compound C1=CC=CC2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21 NAQWICRLNQSPPW-UHFFFAOYSA-N 0.000 description 1
- UXNCDAQNSQBHEN-UHFFFAOYSA-N 1,2,3,4-tetrahydrophenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1CCCC2 UXNCDAQNSQBHEN-UHFFFAOYSA-N 0.000 description 1
- IMSHIOJKUPGIOQ-UHFFFAOYSA-N 1,2,3,4-tetrahydrophenazine Chemical compound C1=CC=C2N=C(CCCC3)C3=NC2=C1 IMSHIOJKUPGIOQ-UHFFFAOYSA-N 0.000 description 1
- QEPTXDCPBXMWJC-UHFFFAOYSA-N 1,2,3-trichloronaphthalene Chemical compound C1=CC=C2C(Cl)=C(Cl)C(Cl)=CC2=C1 QEPTXDCPBXMWJC-UHFFFAOYSA-N 0.000 description 1
- BBAHZGDEGNYDBK-UHFFFAOYSA-N 1,2,3-triphenylazulene Chemical compound C1=CC=CC=C1C(C(=C1C=CC=CC=C11)C=2C=CC=CC=2)=C1C1=CC=CC=C1 BBAHZGDEGNYDBK-UHFFFAOYSA-N 0.000 description 1
- GDAXJBDYNVDMDF-UHFFFAOYSA-N 1,2,4-benzotriazine Chemical compound N1=NC=NC2=CC=CC=C21 GDAXJBDYNVDMDF-UHFFFAOYSA-N 0.000 description 1
- UPOYJEBBRHJJNZ-UHFFFAOYSA-N 1,2,4-tribromonaphthalene Chemical compound C1=CC=CC2=C(Br)C(Br)=CC(Br)=C21 UPOYJEBBRHJJNZ-UHFFFAOYSA-N 0.000 description 1
- ALMJWSDQPWFZQM-UHFFFAOYSA-N 1,2,4-triphenylnaphthalene Chemical compound C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=C(C=CC=C2)C2=C1C1=CC=CC=C1 ALMJWSDQPWFZQM-UHFFFAOYSA-N 0.000 description 1
- IIBSQRLACOMCBX-UHFFFAOYSA-N 1,2,7-trichloroanthracene Chemical compound C1=CC(Cl)=C(Cl)C2=CC3=CC(Cl)=CC=C3C=C21 IIBSQRLACOMCBX-UHFFFAOYSA-N 0.000 description 1
- GCMNJUJAKQGROZ-UHFFFAOYSA-N 1,2-Dihydroquinolin-2-imine Chemical compound C1=CC=CC2=NC(N)=CC=C21 GCMNJUJAKQGROZ-UHFFFAOYSA-N 0.000 description 1
- WOAHJDHKFWSLKE-UHFFFAOYSA-N 1,2-benzoquinone Chemical compound O=C1C=CC=CC1=O WOAHJDHKFWSLKE-UHFFFAOYSA-N 0.000 description 1
- JYIOKRNHGIOENM-UHFFFAOYSA-N 1,2-bis(4-methyl-2-phenylnaphthalen-1-yl)ethane-1,2-dione Chemical compound C=1C=CC=CC=1C=1C=C(C)C2=CC=CC=C2C=1C(=O)C(=O)C=1C2=CC=CC=C2C(C)=CC=1C1=CC=CC=C1 JYIOKRNHGIOENM-UHFFFAOYSA-N 0.000 description 1
- CZAVPKZCPBVPDJ-UHFFFAOYSA-N 1,2-bis[2-(2-phenylphenyl)phenyl]benzene Chemical group C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC=C1 CZAVPKZCPBVPDJ-UHFFFAOYSA-N 0.000 description 1
- IAUKWGFWINVWKS-UHFFFAOYSA-N 1,2-di(propan-2-yl)naphthalene Chemical compound C1=CC=CC2=C(C(C)C)C(C(C)C)=CC=C21 IAUKWGFWINVWKS-UHFFFAOYSA-N 0.000 description 1
- MOXLHAPKZWTHEX-UHFFFAOYSA-N 1,2-dichloronaphthalene Chemical compound C1=CC=CC2=C(Cl)C(Cl)=CC=C21 MOXLHAPKZWTHEX-UHFFFAOYSA-N 0.000 description 1
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- SSDCYRGPZNHDOL-UHFFFAOYSA-N 1,2-dihydroanthracene Chemical compound C1=CC=C2C=C(C=CCC3)C3=CC2=C1 SSDCYRGPZNHDOL-UHFFFAOYSA-N 0.000 description 1
- KEIFWROAQVVDBN-UHFFFAOYSA-N 1,2-dihydronaphthalene Chemical compound C1=CC=C2C=CCCC2=C1 KEIFWROAQVVDBN-UHFFFAOYSA-N 0.000 description 1
- ZTNJGMFHJYGMDR-UHFFFAOYSA-N 1,2-diisocyanatoethane Chemical compound O=C=NCCN=C=O ZTNJGMFHJYGMDR-UHFFFAOYSA-N 0.000 description 1
- ASWRLTWCQYWZFL-UHFFFAOYSA-N 1,2-dimethylphenanthrene Chemical compound C1=CC=C2C3=CC=C(C)C(C)=C3C=CC2=C1 ASWRLTWCQYWZFL-UHFFFAOYSA-N 0.000 description 1
- MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical compound C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 description 1
- AXRVRVKZFJPHBH-UHFFFAOYSA-N 1,3,4-triphenylpyrazole Chemical compound C1=C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=NN1C1=CC=CC=C1 AXRVRVKZFJPHBH-UHFFFAOYSA-N 0.000 description 1
- NNAUDJVNWLIGDT-UHFFFAOYSA-N 1,3,5,7-tetrahydroxyanthracene-9,10-dione Chemical compound OC1=CC(O)=C2C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C1 NNAUDJVNWLIGDT-UHFFFAOYSA-N 0.000 description 1
- QVWVCIZBGCUEGY-UHFFFAOYSA-N 1,3,5,8-tetrabromonaphthalene Chemical compound BrC1=CC=C(Br)C2=CC(Br)=CC(Br)=C21 QVWVCIZBGCUEGY-UHFFFAOYSA-N 0.000 description 1
- JHMMNVQXKFUCCZ-VOTSOKGWSA-N 1,3,5-trinitro-2-[(e)-2-phenylethenyl]benzene Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1\C=C\C1=CC=CC=C1 JHMMNVQXKFUCCZ-VOTSOKGWSA-N 0.000 description 1
- YQDSXDPQYUXRDP-UHFFFAOYSA-N 1,3,5-triphenylpyrazole Chemical compound C=1C(C=2C=CC=CC=2)=NN(C=2C=CC=CC=2)C=1C1=CC=CC=C1 YQDSXDPQYUXRDP-UHFFFAOYSA-N 0.000 description 1
- BULBRUKKSUUPNT-UHFFFAOYSA-N 1,3,6,7-tetrachloronaphthalene Chemical compound C1=C(Cl)C(Cl)=CC2=CC(Cl)=CC(Cl)=C21 BULBRUKKSUUPNT-UHFFFAOYSA-N 0.000 description 1
- XYTKCJHHXQVFCK-UHFFFAOYSA-N 1,3,8-trimethylnaphthalene Chemical compound CC1=CC=CC2=CC(C)=CC(C)=C21 XYTKCJHHXQVFCK-UHFFFAOYSA-N 0.000 description 1
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- IKYNWXNXXHWHLL-UHFFFAOYSA-N 1,3-diisocyanatopropane Chemical compound O=C=NCCCN=C=O IKYNWXNXXHWHLL-UHFFFAOYSA-N 0.000 description 1
- ZKSVYBRJSMBDMV-UHFFFAOYSA-N 1,3-diphenyl-2-benzofuran Chemical compound C1=CC=CC=C1C1=C2C=CC=CC2=C(C=2C=CC=CC=2)O1 ZKSVYBRJSMBDMV-UHFFFAOYSA-N 0.000 description 1
- LQUBXCVRJZGBLM-UHFFFAOYSA-N 1,3-diphenylpyrazole Chemical compound C1=CN(C=2C=CC=CC=2)N=C1C1=CC=CC=C1 LQUBXCVRJZGBLM-UHFFFAOYSA-N 0.000 description 1
- QCJRALCEWIEDED-UHFFFAOYSA-N 1,4,5-tribromonaphthalene Chemical compound C1=CC=C2C(Br)=CC=C(Br)C2=C1Br QCJRALCEWIEDED-UHFFFAOYSA-N 0.000 description 1
- GAAAZLAWPPVHHL-UHFFFAOYSA-N 1,4,5-triphenylpyrazole Chemical compound C1=NN(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 GAAAZLAWPPVHHL-UHFFFAOYSA-N 0.000 description 1
- 239000005967 1,4-Dimethylnaphthalene Substances 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- IBGUDZMIAZLJNY-UHFFFAOYSA-N 1,4-dibromonaphthalene Chemical compound C1=CC=C2C(Br)=CC=C(Br)C2=C1 IBGUDZMIAZLJNY-UHFFFAOYSA-N 0.000 description 1
- QGFHQIHSEPNVKV-UHFFFAOYSA-N 1,4-dichloroanthracene Chemical compound C1=CC=C2C=C3C(Cl)=CC=C(Cl)C3=CC2=C1 QGFHQIHSEPNVKV-UHFFFAOYSA-N 0.000 description 1
- VTEZPNHRQSIHFM-UHFFFAOYSA-N 1,4-difluoronaphthalene Chemical compound C1=CC=C2C(F)=CC=C(F)C2=C1 VTEZPNHRQSIHFM-UHFFFAOYSA-N 0.000 description 1
- FUPIVZHYVSCYLX-UHFFFAOYSA-N 1,4-dihydronaphthalene Chemical compound C1=CC=C2CC=CCC2=C1 FUPIVZHYVSCYLX-UHFFFAOYSA-N 0.000 description 1
- SZGRYHOWWRNMFJ-UHFFFAOYSA-N 1,4-diiodonaphthalene Chemical compound C1=CC=C2C(I)=CC=C(I)C2=C1 SZGRYHOWWRNMFJ-UHFFFAOYSA-N 0.000 description 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- GXLSPHDWEPSUIB-UHFFFAOYSA-N 1,4-diphenylnaphthalene Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=CC=C1C1=CC=CC=C1 GXLSPHDWEPSUIB-UHFFFAOYSA-N 0.000 description 1
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 1
- ZBQZXTBAGBTUAD-UHFFFAOYSA-N 1,5-dichloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1Cl ZBQZXTBAGBTUAD-UHFFFAOYSA-N 0.000 description 1
- IDCXLYCLPHRSAZ-UHFFFAOYSA-N 1,5-diphenylpyrazole Chemical compound C=1C=CC=CC=1N1N=CC=C1C1=CC=CC=C1 IDCXLYCLPHRSAZ-UHFFFAOYSA-N 0.000 description 1
- FCERNNLMTCOKHX-UHFFFAOYSA-N 1,5-diphenyltetrazole Chemical compound C1=CC=CC=C1C1=NN=NN1C1=CC=CC=C1 FCERNNLMTCOKHX-UHFFFAOYSA-N 0.000 description 1
- CEDZMDSZTVUPSP-UHFFFAOYSA-N 1,6-dichloronaphthalene Chemical compound ClC1=CC=CC2=CC(Cl)=CC=C21 CEDZMDSZTVUPSP-UHFFFAOYSA-N 0.000 description 1
- AFGNPFWWBHDPEN-UHFFFAOYSA-N 1,6-dioxacyclododecane-2,5-dione Chemical compound O=C1CCC(=O)OCCCCCCO1 AFGNPFWWBHDPEN-UHFFFAOYSA-N 0.000 description 1
- VQBIYCQGHAHVPN-UHFFFAOYSA-N 1,7-dichloronaphthalene Chemical compound C1=CC=C(Cl)C2=CC(Cl)=CC=C21 VQBIYCQGHAHVPN-UHFFFAOYSA-N 0.000 description 1
- OZKOMUDCMCEDTM-UHFFFAOYSA-N 1,7-phenanthroline Chemical compound C1=CC=C2C3=NC=CC=C3C=CC2=N1 OZKOMUDCMCEDTM-UHFFFAOYSA-N 0.000 description 1
- CFIOJKIANKORPY-UHFFFAOYSA-N 1,8-dibenzylnaphthalene Chemical compound C=1C=CC2=CC=CC(CC=3C=CC=CC=3)=C2C=1CC1=CC=CC=C1 CFIOJKIANKORPY-UHFFFAOYSA-N 0.000 description 1
- SXWPIGKEISLSNQ-UHFFFAOYSA-N 1,8-dioxacyclooctadecane-9,18-dione Chemical compound O=C1CCCCCCCCC(=O)OCCCCCCO1 SXWPIGKEISLSNQ-UHFFFAOYSA-N 0.000 description 1
- POTFVITYTOBTKF-UHFFFAOYSA-N 1-(1,4-dimethylcyclohexa-2,4-dien-1-yl)-2-methylpiperazine Chemical compound C1(CC=C(C=C1)C)(C)N1C(CNCC1)C POTFVITYTOBTKF-UHFFFAOYSA-N 0.000 description 1
- LVZBNQAITQCBEC-UHFFFAOYSA-N 1-(1-chloroethyl)naphthalene Chemical compound C1=CC=C2C(C(Cl)C)=CC=CC2=C1 LVZBNQAITQCBEC-UHFFFAOYSA-N 0.000 description 1
- UICXTANXZJJIBC-UHFFFAOYSA-N 1-(1-hydroperoxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(OO)CCCCC1 UICXTANXZJJIBC-UHFFFAOYSA-N 0.000 description 1
- SEJFWAWYAJTLJD-UHFFFAOYSA-N 1-(2,3-dinitrophenoxy)-2,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(OC=2C(=C(C=CC=2)[N+]([O-])=O)[N+]([O-])=O)=C1[N+]([O-])=O SEJFWAWYAJTLJD-UHFFFAOYSA-N 0.000 description 1
- ZYFTVCJVNRKBCC-UHFFFAOYSA-N 1-(2-methylpropyl)naphthalene Chemical compound C1=CC=C2C(CC(C)C)=CC=CC2=C1 ZYFTVCJVNRKBCC-UHFFFAOYSA-N 0.000 description 1
- OKDWGFQXJYJNIJ-UHFFFAOYSA-N 1-(2-methylquinolin-3-yl)ethanone Chemical compound C1=CC=C2N=C(C)C(C(=O)C)=CC2=C1 OKDWGFQXJYJNIJ-UHFFFAOYSA-N 0.000 description 1
- RLGXDIGUNMDWRX-UHFFFAOYSA-N 1-(2-phenylethyl)naphthalene Chemical compound C=1C=CC2=CC=CC=C2C=1CCC1=CC=CC=C1 RLGXDIGUNMDWRX-UHFFFAOYSA-N 0.000 description 1
- OUZPHFHCYBXKAY-UHFFFAOYSA-N 1-(3,4-dihydronaphthalen-1-yl)ethanone Chemical compound C1=CC=C2C(C(=O)C)=CCCC2=C1 OUZPHFHCYBXKAY-UHFFFAOYSA-N 0.000 description 1
- XPIBNCGHRJCREA-UHFFFAOYSA-N 1-(7-bromonaphthalen-1-yl)ethanone Chemical compound C1=C(Br)C=C2C(C(=O)C)=CC=CC2=C1 XPIBNCGHRJCREA-UHFFFAOYSA-N 0.000 description 1
- VBPBWRXUZDIQHT-UHFFFAOYSA-N 1-(8-acetyldibenzothiophen-2-yl)ethanone Chemical compound C1=C(C(C)=O)C=C2C3=CC(C(=O)C)=CC=C3SC2=C1 VBPBWRXUZDIQHT-UHFFFAOYSA-N 0.000 description 1
- TXIBBNMZMRYADF-UHFFFAOYSA-N 1-(naphthalen-1-yldisulfanyl)naphthalene Chemical compound C1=CC=C2C(SSC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 TXIBBNMZMRYADF-UHFFFAOYSA-N 0.000 description 1
- RPGQJXGITZORAG-UHFFFAOYSA-N 1-(nitromethyl)naphthalene Chemical compound C1=CC=C2C(C[N+](=O)[O-])=CC=CC2=C1 RPGQJXGITZORAG-UHFFFAOYSA-N 0.000 description 1
- ZINRVIQBCHAZMM-UHFFFAOYSA-N 1-Amino-2,4-dibromoanthraquinone Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(Br)=CC(Br)=C2N ZINRVIQBCHAZMM-UHFFFAOYSA-N 0.000 description 1
- ZPANWZBSGMDWON-UHFFFAOYSA-N 1-[(2-hydroxynaphthalen-1-yl)methyl]naphthalen-2-ol Chemical compound C1=CC=C2C(CC3=C4C=CC=CC4=CC=C3O)=C(O)C=CC2=C1 ZPANWZBSGMDWON-UHFFFAOYSA-N 0.000 description 1
- WBMGWJGLUWZFEE-UHFFFAOYSA-N 1-[(3,4-dimethoxyphenyl)methyl]-7-hydroxy-2-methylisoquinolin-6-one Chemical compound C1=C(OC)C(OC)=CC=C1CC1=C2C=C(O)C(=O)C=C2C=CN1C WBMGWJGLUWZFEE-UHFFFAOYSA-N 0.000 description 1
- JZZVTXWEIKSEGX-UHFFFAOYSA-N 1-[1-(9,10-dioxoanthracen-1-yl)ethenyl]anthracene-9,10-dione Chemical group O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(=C)C1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O JZZVTXWEIKSEGX-UHFFFAOYSA-N 0.000 description 1
- AUKRZCOZSLQXHA-UHFFFAOYSA-N 1-[1-(9,10-dioxoanthracen-1-yl)ethyl]anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(C)C1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AUKRZCOZSLQXHA-UHFFFAOYSA-N 0.000 description 1
- PIBSPTNFNZNNJZ-UHFFFAOYSA-N 1-[2-(2,4-dinitrophenyl)ethenyl]naphthalene Chemical group [O-][N+](=O)C1=CC([N+](=O)[O-])=CC=C1C=CC1=CC=CC2=CC=CC=C12 PIBSPTNFNZNNJZ-UHFFFAOYSA-N 0.000 description 1
- SADZCJZAODOWTP-UHFFFAOYSA-N 1-[chloro(diphenyl)methyl]naphthalene Chemical compound C=1C=CC=CC=1C(C=1C2=CC=CC=C2C=CC=1)(Cl)C1=CC=CC=C1 SADZCJZAODOWTP-UHFFFAOYSA-N 0.000 description 1
- XNIXNMOSLYVHNW-UHFFFAOYSA-N 1-amino-2,4-dibromo-5-nitroanthracene-9,10-dione Chemical compound O=C1C=2C(N)=C(Br)C=C(Br)C=2C(=O)C2=C1C=CC=C2[N+]([O-])=O XNIXNMOSLYVHNW-UHFFFAOYSA-N 0.000 description 1
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 1
- VPSMSRGGNXFQIO-UHFFFAOYSA-N 1-aminonaphthalene-2-thiol Chemical compound C1=CC=C2C(N)=C(S)C=CC2=C1 VPSMSRGGNXFQIO-UHFFFAOYSA-N 0.000 description 1
- MUVQKFGNPGZBII-UHFFFAOYSA-N 1-anthrol Chemical compound C1=CC=C2C=C3C(O)=CC=CC3=CC2=C1 MUVQKFGNPGZBII-UHFFFAOYSA-N 0.000 description 1
- UNYPOFWEGVYMRJ-UHFFFAOYSA-N 1-azidoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N=[N+]=[N-] UNYPOFWEGVYMRJ-UHFFFAOYSA-N 0.000 description 1
- DZRJNLPOTUVETG-UHFFFAOYSA-N 1-benzofuran-2-yl(phenyl)methanone Chemical compound C=1C2=CC=CC=C2OC=1C(=O)C1=CC=CC=C1 DZRJNLPOTUVETG-UHFFFAOYSA-N 0.000 description 1
- LCFXRSKBJWQHON-UHFFFAOYSA-N 1-benzyl-2-phenylbenzimidazole Chemical compound C=1C=CC=CC=1C1=NC2=CC=CC=C2N1CC1=CC=CC=C1 LCFXRSKBJWQHON-UHFFFAOYSA-N 0.000 description 1
- KTHUKEZOIFYPEH-UHFFFAOYSA-N 1-benzylnaphthalene Chemical compound C=1C=CC2=CC=CC=C2C=1CC1=CC=CC=C1 KTHUKEZOIFYPEH-UHFFFAOYSA-N 0.000 description 1
- WGGLDBIZIQMEGH-UHFFFAOYSA-N 1-bromo-4-ethenylbenzene Chemical compound BrC1=CC=C(C=C)C=C1 WGGLDBIZIQMEGH-UHFFFAOYSA-N 0.000 description 1
- JESBGFNZNSEZMR-UHFFFAOYSA-N 1-bromodibenzothiophene Chemical compound S1C2=CC=CC=C2C2=C1C=CC=C2Br JESBGFNZNSEZMR-UHFFFAOYSA-N 0.000 description 1
- DLKQHBOKULLWDQ-UHFFFAOYSA-N 1-bromonaphthalene Chemical compound C1=CC=C2C(Br)=CC=CC2=C1 DLKQHBOKULLWDQ-UHFFFAOYSA-N 0.000 description 1
- RGJXEFKYMBTAOM-UHFFFAOYSA-N 1-bromophenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1C(Br)=CC=C2 RGJXEFKYMBTAOM-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- URGSMJLDEFDWNX-UHFFFAOYSA-N 1-butylnaphthalene Chemical compound C1=CC=C2C(CCCC)=CC=CC2=C1 URGSMJLDEFDWNX-UHFFFAOYSA-N 0.000 description 1
- VAXHNWJSQXUXMK-UHFFFAOYSA-N 1-carbazol-9-ylprop-2-en-1-one Chemical compound C1=CC=C2N(C(=O)C=C)C3=CC=CC=C3C2=C1 VAXHNWJSQXUXMK-UHFFFAOYSA-N 0.000 description 1
- WTVKFPGVKKXUHG-ZHACJKMWSA-N 1-chloro-2-[(e)-2-phenylethenyl]benzene Chemical compound ClC1=CC=CC=C1\C=C\C1=CC=CC=C1 WTVKFPGVKKXUHG-ZHACJKMWSA-N 0.000 description 1
- DNJRKFKAFWSXSE-UHFFFAOYSA-N 1-chloro-2-ethenoxyethane Chemical compound ClCCOC=C DNJRKFKAFWSXSE-UHFFFAOYSA-N 0.000 description 1
- IEDBAGGSOLFBBH-UHFFFAOYSA-N 1-chloro-4-methylphthalazine Chemical compound C1=CC=C2C(C)=NN=C(Cl)C2=C1 IEDBAGGSOLFBBH-UHFFFAOYSA-N 0.000 description 1
- SRIHSAFSOOUEGL-UHFFFAOYSA-N 1-chloroanthracene Chemical compound C1=CC=C2C=C3C(Cl)=CC=CC3=CC2=C1 SRIHSAFSOOUEGL-UHFFFAOYSA-N 0.000 description 1
- MSQCQINLJMEVNJ-UHFFFAOYSA-N 1-chloroisoquinoline Chemical compound C1=CC=C2C(Cl)=NC=CC2=C1 MSQCQINLJMEVNJ-UHFFFAOYSA-N 0.000 description 1
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
- IYTUPMAAMJDPCR-UHFFFAOYSA-N 1-chlorophenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1C(Cl)=CC=C2 IYTUPMAAMJDPCR-UHFFFAOYSA-N 0.000 description 1
- NTHRMQKFNGUJPH-UHFFFAOYSA-N 1-dibenzothiophen-2-ylethanone Chemical compound C1=CC=C2C3=CC(C(=O)C)=CC=C3SC2=C1 NTHRMQKFNGUJPH-UHFFFAOYSA-N 0.000 description 1
- GJNDXPONYMDBFD-UHFFFAOYSA-N 1-ethenoxy-2,2-dimethylpropane Chemical compound CC(C)(C)COC=C GJNDXPONYMDBFD-UHFFFAOYSA-N 0.000 description 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 description 1
- FXMZAGUYSCLBFQ-UHFFFAOYSA-N 1-ethenyl-2h-1,2,4-triazine Chemical compound C=CN1NC=NC=C1 FXMZAGUYSCLBFQ-UHFFFAOYSA-N 0.000 description 1
- OKHGMSQINQQCIE-UHFFFAOYSA-N 1-ethenylbenzotriazole Chemical compound C1=CC=C2N(C=C)N=NC2=C1 OKHGMSQINQQCIE-UHFFFAOYSA-N 0.000 description 1
- UGMRKNAZEKUAQS-UHFFFAOYSA-N 1-ethenylphenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1C(C=C)=CC=C2 UGMRKNAZEKUAQS-UHFFFAOYSA-N 0.000 description 1
- ZMXIYERNXPIYFR-UHFFFAOYSA-N 1-ethylnaphthalene Chemical compound C1=CC=C2C(CC)=CC=CC2=C1 ZMXIYERNXPIYFR-UHFFFAOYSA-N 0.000 description 1
- KAXRXNJKBMDQHE-UHFFFAOYSA-N 1-ethylphenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1C(CC)=CC=C2 KAXRXNJKBMDQHE-UHFFFAOYSA-N 0.000 description 1
- CWLKTJOTWITYSI-UHFFFAOYSA-N 1-fluoronaphthalene Chemical compound C1=CC=C2C(F)=CC=CC2=C1 CWLKTJOTWITYSI-UHFFFAOYSA-N 0.000 description 1
- VTHAYUPMFCMKIH-UHFFFAOYSA-N 1-heptylsulfonylheptane Chemical compound CCCCCCCS(=O)(=O)CCCCCCC VTHAYUPMFCMKIH-UHFFFAOYSA-N 0.000 description 1
- HBOOMWHZBIPTMN-UHFFFAOYSA-N 1-hexylsulfonylhexane Chemical compound CCCCCCS(=O)(=O)CCCCCC HBOOMWHZBIPTMN-UHFFFAOYSA-N 0.000 description 1
- QFNFXYPFSYJCDF-UHFFFAOYSA-N 1-hydroxy-2h-isoquinolin-3-one Chemical compound C1=CC=CC2=C(O)NC(=O)C=C21 QFNFXYPFSYJCDF-UHFFFAOYSA-N 0.000 description 1
- SVRNCBGWUMMBQB-UHFFFAOYSA-N 1-hydroxyphenazine Chemical compound C1=CC=C2N=C3C(O)=CC=CC3=NC2=C1 SVRNCBGWUMMBQB-UHFFFAOYSA-N 0.000 description 1
- NHPPIJMARIVBGU-UHFFFAOYSA-N 1-iodonaphthalene Chemical compound C1=CC=C2C(I)=CC=CC2=C1 NHPPIJMARIVBGU-UHFFFAOYSA-N 0.000 description 1
- WDQUKJXPPPPCGP-UHFFFAOYSA-N 1-iodophenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1C(I)=CC=C2 WDQUKJXPPPPCGP-UHFFFAOYSA-N 0.000 description 1
- PQKKDBJPQMUFQI-UHFFFAOYSA-N 1-methoxy-4-[4-(4-methoxynaphthalen-1-yl)buta-1,3-dienyl]naphthalene Chemical compound C12=CC=CC=C2C(OC)=CC=C1C=CC=CC1=CC=C(OC)C2=CC=CC=C12 PQKKDBJPQMUFQI-UHFFFAOYSA-N 0.000 description 1
- QYEMNJMSULGQRD-UHFFFAOYSA-N 1-methyl-2-quinolone Chemical compound C1=CC=C2C=CC(=O)N(C)C2=C1 QYEMNJMSULGQRD-UHFFFAOYSA-N 0.000 description 1
- CXQGBMJSAAFWDF-UHFFFAOYSA-N 1-methyl-3-phenylindole Chemical compound C12=CC=CC=C2N(C)C=C1C1=CC=CC=C1 CXQGBMJSAAFWDF-UHFFFAOYSA-N 0.000 description 1
- AQQUNJMVAKJGKR-UHFFFAOYSA-N 1-methyl-3-phenylpyrazole Chemical compound CN1C=CC(C=2C=CC=CC=2)=N1 AQQUNJMVAKJGKR-UHFFFAOYSA-N 0.000 description 1
- NLHYNCJBWXKZGP-UHFFFAOYSA-N 1-methyl-5-phenylpyrazole Chemical compound CN1N=CC=C1C1=CC=CC=C1 NLHYNCJBWXKZGP-UHFFFAOYSA-N 0.000 description 1
- VXGOQVMIGNMUGC-UHFFFAOYSA-N 1-methylacridine Chemical compound C1=CC=C2C=C3C(C)=CC=CC3=NC2=C1 VXGOQVMIGNMUGC-UHFFFAOYSA-N 0.000 description 1
- SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 description 1
- VDJWDDNALBETLW-UHFFFAOYSA-N 1-naphthalen-1-yl-3H-naphthalene-2,2-diamine Chemical group C1=CC=C2C(C3=C4C=CC=CC4=CCC3(N)N)=CC=CC2=C1 VDJWDDNALBETLW-UHFFFAOYSA-N 0.000 description 1
- AEZUOROLJYRAKU-UHFFFAOYSA-N 1-naphthalen-1-yloctadecan-1-one Chemical compound C1=CC=C2C(C(=O)CCCCCCCCCCCCCCCCC)=CC=CC2=C1 AEZUOROLJYRAKU-UHFFFAOYSA-N 0.000 description 1
- QFLRYLKUSFJFTK-UHFFFAOYSA-N 1-naphthalen-1-ylpropan-1-one Chemical compound C1=CC=C2C(C(=O)CC)=CC=CC2=C1 QFLRYLKUSFJFTK-UHFFFAOYSA-N 0.000 description 1
- OSGZQTUEDXNVLY-UHFFFAOYSA-N 1-naphthalen-2-yl-3-phenylpropane-1,3-dione Chemical compound C=1C=C2C=CC=CC2=CC=1C(=O)CC(=O)C1=CC=CC=C1 OSGZQTUEDXNVLY-UHFFFAOYSA-N 0.000 description 1
- NFJOLQJZODADPL-UHFFFAOYSA-N 1-naphthalen-2-ylbutane-1,3-dione Chemical compound C1=CC=CC2=CC(C(=O)CC(=O)C)=CC=C21 NFJOLQJZODADPL-UHFFFAOYSA-N 0.000 description 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical class C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- ALTGNKHNQHUIKE-UHFFFAOYSA-N 1-nitro-10h-phenothiazine Chemical compound S1C2=CC=CC=C2NC2=C1C=CC=C2[N+](=O)[O-] ALTGNKHNQHUIKE-UHFFFAOYSA-N 0.000 description 1
- DEEULBIVHZVMHX-UHFFFAOYSA-N 1-nitroacridine Chemical compound C1=CC=C2C=C3C([N+](=O)[O-])=CC=CC3=NC2=C1 DEEULBIVHZVMHX-UHFFFAOYSA-N 0.000 description 1
- JBDYKGMNMDIHFL-UHFFFAOYSA-N 1-nitroanthracene Chemical compound C1=CC=C2C=C3C([N+](=O)[O-])=CC=CC3=CC2=C1 JBDYKGMNMDIHFL-UHFFFAOYSA-N 0.000 description 1
- RJKGJBPXVHTNJL-UHFFFAOYSA-N 1-nitronaphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=CC2=C1 RJKGJBPXVHTNJL-UHFFFAOYSA-N 0.000 description 1
- SGNWFFATVZVHNF-UHFFFAOYSA-N 1-nitrophenanthrene Chemical compound C1=CC2=CC=CC=C2C2=C1C([N+](=O)[O-])=CC=C2 SGNWFFATVZVHNF-UHFFFAOYSA-N 0.000 description 1
- RCSMBBHQCLEWMO-UHFFFAOYSA-N 1-nitrosoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N=O RCSMBBHQCLEWMO-UHFFFAOYSA-N 0.000 description 1
- YXAOOTNFFAQIPZ-UHFFFAOYSA-N 1-nitrosonaphthalen-2-ol Chemical compound C1=CC=CC2=C(N=O)C(O)=CC=C21 YXAOOTNFFAQIPZ-UHFFFAOYSA-N 0.000 description 1
- NLUGCAKOZAODBF-UHFFFAOYSA-N 1-pentylsulfonylpentane Chemical compound CCCCCS(=O)(=O)CCCCC NLUGCAKOZAODBF-UHFFFAOYSA-N 0.000 description 1
- FFNRKAWQIXXMNB-UHFFFAOYSA-N 1-phenanthren-1-ylethanone Chemical compound C1=CC2=CC=CC=C2C2=C1C(C(=O)C)=CC=C2 FFNRKAWQIXXMNB-UHFFFAOYSA-N 0.000 description 1
- MWDUHLRRTSHHSG-UHFFFAOYSA-N 1-phenanthren-2-ylpropan-1-one Chemical compound C1=CC=C2C3=CC=C(C(=O)CC)C=C3C=CC2=C1 MWDUHLRRTSHHSG-UHFFFAOYSA-N 0.000 description 1
- ZBJLUVHQIPUCPM-UHFFFAOYSA-N 1-phenylbenzotriazole Chemical compound C1=CC=CC=C1N1C2=CC=CC=C2N=N1 ZBJLUVHQIPUCPM-UHFFFAOYSA-N 0.000 description 1
- KDEORSBCWLFTFX-UHFFFAOYSA-N 1-phenyliminonaphthalen-2-one Chemical compound O=C1C=CC2=CC=CC=C2C1=NC1=CC=CC=C1 KDEORSBCWLFTFX-UHFFFAOYSA-N 0.000 description 1
- LPCWDYWZIWDTCV-UHFFFAOYSA-N 1-phenylisoquinoline Chemical compound C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 LPCWDYWZIWDTCV-UHFFFAOYSA-N 0.000 description 1
- GEZGAZKEOUKLBR-UHFFFAOYSA-N 1-phenylpyrrole Chemical compound C1=CC=CN1C1=CC=CC=C1 GEZGAZKEOUKLBR-UHFFFAOYSA-N 0.000 description 1
- RJFCFNWLPJRCLR-UHFFFAOYSA-N 1-prop-2-enylnaphthalene Chemical compound C1=CC=C2C(CC=C)=CC=CC2=C1 RJFCFNWLPJRCLR-UHFFFAOYSA-N 0.000 description 1
- HMAMGXMFMCAOPV-UHFFFAOYSA-N 1-propylnaphthalene Chemical compound C1=CC=C2C(CCC)=CC=CC2=C1 HMAMGXMFMCAOPV-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- VDOLRBJLUIFCGO-UHFFFAOYSA-N 10-(2-pyrrolidin-1-ylethyl)phenothiazine;hydrochloride Chemical compound Cl.C12=CC=CC=C2SC2=CC=CC=C2N1CCN1CCCC1 VDOLRBJLUIFCGO-UHFFFAOYSA-N 0.000 description 1
- NWESITKKFMZEDY-UHFFFAOYSA-N 10-bromophenanthren-9-ol Chemical compound C1=CC=C2C(O)=C(Br)C3=CC=CC=C3C2=C1 NWESITKKFMZEDY-UHFFFAOYSA-N 0.000 description 1
- UQJOOEPGSRMVJJ-UHFFFAOYSA-N 10-chlorobenzo[g]quinoline Chemical compound C1=CN=C2C(Cl)=C(C=CC=C3)C3=CC2=C1 UQJOOEPGSRMVJJ-UHFFFAOYSA-N 0.000 description 1
- XZPNVGKRRGOOMS-UHFFFAOYSA-N 10-methyl-5h-phenazine Chemical compound C1=CC=C2N(C)C3=CC=CC=C3NC2=C1 XZPNVGKRRGOOMS-UHFFFAOYSA-N 0.000 description 1
- PDONJLWNMMAAGY-UHFFFAOYSA-N 10-methyl-5h-phenazine-2-carbonitrile Chemical compound C1=C(C#N)C=C2N(C)C3=CC=CC=C3NC2=C1 PDONJLWNMMAAGY-UHFFFAOYSA-N 0.000 description 1
- PHUUSOJITOMTEZ-UHFFFAOYSA-N 10-methylanthracen-1-ol Chemical compound C1=CC=C2C(C)=C(C=CC=C3)C3=CC2=C1O PHUUSOJITOMTEZ-UHFFFAOYSA-N 0.000 description 1
- GSWNVMSLPNWJIJ-UHFFFAOYSA-N 10-phenylanthracen-1-ol Chemical compound C12=CC=CC=C2C=C2C(O)=CC=CC2=C1C1=CC=CC=C1 GSWNVMSLPNWJIJ-UHFFFAOYSA-N 0.000 description 1
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 description 1
- MIAQOBQBLCUGNT-UHFFFAOYSA-N 10h-phenothiazin-3-amine Chemical compound C1=CC=C2SC3=CC(N)=CC=C3NC2=C1 MIAQOBQBLCUGNT-UHFFFAOYSA-N 0.000 description 1
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 description 1
- LQRUVABVXQZQMV-UHFFFAOYSA-N 11h-indolo[3,2-c]quinoline Chemical compound C1=NC2=CC=CC=C2C2=C1C1=CC=CC=C1N2 LQRUVABVXQZQMV-UHFFFAOYSA-N 0.000 description 1
- IJJMQFOFFIWMNN-UHFFFAOYSA-N 12-oxapentacyclo[12.8.0.02,11.03,8.015,20]docosa-1(14),2(11),3,5,7,9,15,17,19,21-decaene Chemical compound C1=CC=CC2=C3COC4=CC=C(C=CC=C5)C5=C4C3=CC=C21 IJJMQFOFFIWMNN-UHFFFAOYSA-N 0.000 description 1
- IDAUIDYDSFARON-UHFFFAOYSA-N 12h-naphtho[2,3-h][1,2]benzoxazine Chemical compound C1=NOC2=C3CC4=CC=CC=C4C=C3C=CC2=C1 IDAUIDYDSFARON-UHFFFAOYSA-N 0.000 description 1
- IWKTVWFSQDLTHC-UHFFFAOYSA-N 1H-imidazol-2-yl(phenyl)diazene Chemical compound C1=CNC(N=NC=2C=CC=CC=2)=N1 IWKTVWFSQDLTHC-UHFFFAOYSA-N 0.000 description 1
- FCXXTPYCFGLOKH-UHFFFAOYSA-N 1H-imidazol-2-yl-(2-methyl-4-phenylimidazol-2-yl)diazene Chemical compound CC1(N=CC(=N1)C1=CC=CC=C1)N=NC=1NC=CN=1 FCXXTPYCFGLOKH-UHFFFAOYSA-N 0.000 description 1
- AAQTWLBJPNLKHT-UHFFFAOYSA-N 1H-perimidine Chemical compound N1C=NC2=CC=CC3=CC=CC1=C32 AAQTWLBJPNLKHT-UHFFFAOYSA-N 0.000 description 1
- KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Substances C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 description 1
- DMSSTTLDFWKBSX-UHFFFAOYSA-N 1h-1,2,3-benzotriazin-4-one Chemical compound C1=CC=C2C(=O)N=NNC2=C1 DMSSTTLDFWKBSX-UHFFFAOYSA-N 0.000 description 1
- SOHTXRQJQMFAPQ-UHFFFAOYSA-N 1h-1,2,3-benzotriazine-4-thione Chemical compound C1=CC=C2C(=S)N=NNC2=C1 SOHTXRQJQMFAPQ-UHFFFAOYSA-N 0.000 description 1
- UFMBERDMCRCVSM-UHFFFAOYSA-N 1h-cinnolin-4-one Chemical compound C1=CC=C2C(O)=CN=NC2=C1 UFMBERDMCRCVSM-UHFFFAOYSA-N 0.000 description 1
- BHZXGLRVKIDNND-UHFFFAOYSA-N 1h-cyclopenta[c]cinnoline Chemical compound C1=CC=CC2=C3CC=CC3=NN=C21 BHZXGLRVKIDNND-UHFFFAOYSA-N 0.000 description 1
- APDMFICDKLFJJL-UHFFFAOYSA-N 1h-pyrazolo[4,3-b]quinoxaline Chemical compound C1=CC=C2N=C3C=NNC3=NC2=C1 APDMFICDKLFJJL-UHFFFAOYSA-N 0.000 description 1
- IVCGJOSPVGENCT-UHFFFAOYSA-N 1h-pyrrolo[2,3-f]quinoline Chemical class N1=CC=CC2=C(NC=C3)C3=CC=C21 IVCGJOSPVGENCT-UHFFFAOYSA-N 0.000 description 1
- KXZSVYHFYHTNBI-UHFFFAOYSA-N 1h-quinoline-2-thione Chemical compound C1=CC=CC2=NC(S)=CC=C21 KXZSVYHFYHTNBI-UHFFFAOYSA-N 0.000 description 1
- OIXJTNWUBMSVJM-UHFFFAOYSA-N 2,10-dioxatricyclo[9.2.2.14,8]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-3,9-dione Chemical compound O1C(=O)C(C=2)=CC=CC=2C(=O)OC2=CC=C1C=C2 OIXJTNWUBMSVJM-UHFFFAOYSA-N 0.000 description 1
- CISIJYCKDJSTMX-UHFFFAOYSA-N 2,2-dichloroethenylbenzene Chemical compound ClC(Cl)=CC1=CC=CC=C1 CISIJYCKDJSTMX-UHFFFAOYSA-N 0.000 description 1
- DFZGDHCABHGZOB-UHFFFAOYSA-N 2,3,5,8-tetrachloronaphthalene-1,4-dione Chemical compound C1=CC(Cl)=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1Cl DFZGDHCABHGZOB-UHFFFAOYSA-N 0.000 description 1
- FBNAYEYTRHHEOB-UHFFFAOYSA-N 2,3,5-triphenyl-1,3-dihydropyrazole Chemical compound N1N(C=2C=CC=CC=2)C(C=2C=CC=CC=2)C=C1C1=CC=CC=C1 FBNAYEYTRHHEOB-UHFFFAOYSA-N 0.000 description 1
- GBCJQOITJVEDQO-UHFFFAOYSA-N 2,3,5-triphenyl-1h-pyrrole Chemical compound C1=C(C=2C=CC=CC=2)NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 GBCJQOITJVEDQO-UHFFFAOYSA-N 0.000 description 1
- SKGXUFZRYNGFJS-UHFFFAOYSA-N 2,3-dichloronaphthalene Chemical compound C1=CC=C2C=C(Cl)C(Cl)=CC2=C1 SKGXUFZRYNGFJS-UHFFFAOYSA-N 0.000 description 1
- KWVNKWCJDAWNAE-UHFFFAOYSA-N 2,3-dichloroquinoline Chemical compound C1=CC=C2N=C(Cl)C(Cl)=CC2=C1 KWVNKWCJDAWNAE-UHFFFAOYSA-N 0.000 description 1
- KQBXYYMELBQTFL-UHFFFAOYSA-N 2,3-dihydrocyclopenta[a]naphthalen-1-one Chemical compound C1=CC=CC2=C3C(=O)CCC3=CC=C21 KQBXYYMELBQTFL-UHFFFAOYSA-N 0.000 description 1
- KGLPWQKSKUVKMJ-UHFFFAOYSA-N 2,3-dihydrophthalazine-1,4-dione Chemical compound C1=CC=C2C(=O)NNC(=O)C2=C1 KGLPWQKSKUVKMJ-UHFFFAOYSA-N 0.000 description 1
- GYGKJNGSQQORRG-UHFFFAOYSA-N 2,3-diphenyl-1h-indole Chemical compound C1=CC=CC=C1C1=C(C=2C=CC=CC=2)C2=CC=CC=C2N1 GYGKJNGSQQORRG-UHFFFAOYSA-N 0.000 description 1
- VNMNSTIGSQBDPI-UHFFFAOYSA-N 2,3-diphenyl-1h-pyrrole Chemical compound N1C=CC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 VNMNSTIGSQBDPI-UHFFFAOYSA-N 0.000 description 1
- DFEAQIRMGGSZDL-UHFFFAOYSA-N 2,3-diphenylnaphthalen-1-ol Chemical compound C=1C=CC=CC=1C1=CC2=CC=CC=C2C(O)=C1C1=CC=CC=C1 DFEAQIRMGGSZDL-UHFFFAOYSA-N 0.000 description 1
- WKHQADGJXFRQJD-UHFFFAOYSA-N 2,4,5-triphenyl-1,3-oxazole Chemical compound C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)O1 WKHQADGJXFRQJD-UHFFFAOYSA-N 0.000 description 1
- RNIPJYFZGXJSDD-UHFFFAOYSA-N 2,4,5-triphenyl-1h-imidazole Chemical compound C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 RNIPJYFZGXJSDD-UHFFFAOYSA-N 0.000 description 1
- SRIFCVCJAZFSKY-UHFFFAOYSA-N 2,4,5-triphenyl-3h-1,3-oxazol-2-ol Chemical compound O1C(O)(C=2C=CC=CC=2)NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 SRIFCVCJAZFSKY-UHFFFAOYSA-N 0.000 description 1
- HBQUOLGAXBYZGR-UHFFFAOYSA-N 2,4,6-triphenyl-1,3,5-triazine Chemical compound C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 HBQUOLGAXBYZGR-UHFFFAOYSA-N 0.000 description 1
- SZKWMQWGJPCXOF-UHFFFAOYSA-N 2,4,6-triphenylpyrimidine Chemical compound C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 SZKWMQWGJPCXOF-UHFFFAOYSA-N 0.000 description 1
- QNBJYUUUYZVIJP-UHFFFAOYSA-N 2,4-dichloroquinoline Chemical compound C1=CC=CC2=NC(Cl)=CC(Cl)=C21 QNBJYUUUYZVIJP-UHFFFAOYSA-N 0.000 description 1
- CUCOSHMIHGWZHP-UHFFFAOYSA-N 2,4-dinitronaphthalene-1-carbaldehyde Chemical compound C1=CC=CC2=C(C=O)C([N+](=O)[O-])=CC([N+]([O-])=O)=C21 CUCOSHMIHGWZHP-UHFFFAOYSA-N 0.000 description 1
- 125000001917 2,4-dinitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1*)[N+]([O-])=O)[N+]([O-])=O 0.000 description 1
- VUPXKQHLZATXTR-UHFFFAOYSA-N 2,4-diphenyl-1,3-oxazole Chemical compound C=1OC(C=2C=CC=CC=2)=NC=1C1=CC=CC=C1 VUPXKQHLZATXTR-UHFFFAOYSA-N 0.000 description 1
- UQJDIUAEJBVXMV-UHFFFAOYSA-N 2,4-diphenylfuran Chemical compound C=1OC(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 UQJDIUAEJBVXMV-UHFFFAOYSA-N 0.000 description 1
- VCOKQFQTBUEGIO-UHFFFAOYSA-N 2,4-diphenylquinoline Chemical compound C1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=C(C=CC=C2)C2=N1 VCOKQFQTBUEGIO-UHFFFAOYSA-N 0.000 description 1
- FKHVUWRLXRMJLF-UHFFFAOYSA-N 2,4-diphenylthiophene Chemical compound C=1SC(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 FKHVUWRLXRMJLF-UHFFFAOYSA-N 0.000 description 1
- CQBMMTIVMOJHSO-UHFFFAOYSA-N 2,5-bis(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione Chemical compound O=C1C=C(SC=2C=CC=CC=2)C(=O)C=C1SC1=CC=CC=C1 CQBMMTIVMOJHSO-UHFFFAOYSA-N 0.000 description 1
- AVAFDZKBQKLGMN-UHFFFAOYSA-N 2,5-dichloroquinazoline Chemical compound ClC1=CC=CC2=NC(Cl)=NC=C21 AVAFDZKBQKLGMN-UHFFFAOYSA-N 0.000 description 1
- DCJKUXYSYJBBRD-UHFFFAOYSA-N 2,5-diphenyl-1,3,4-oxadiazole Chemical compound C1=CC=CC=C1C1=NN=C(C=2C=CC=CC=2)O1 DCJKUXYSYJBBRD-UHFFFAOYSA-N 0.000 description 1
- FHHCKYIBYRNHOZ-UHFFFAOYSA-N 2,5-diphenyl-1h-imidazole Chemical compound C=1N=C(C=2C=CC=CC=2)NC=1C1=CC=CC=C1 FHHCKYIBYRNHOZ-UHFFFAOYSA-N 0.000 description 1
- RJCRXUOYULQDPG-UHFFFAOYSA-N 2,5-diphenyl-1h-pyrrole Chemical compound C=1C=C(C=2C=CC=CC=2)NC=1C1=CC=CC=C1 RJCRXUOYULQDPG-UHFFFAOYSA-N 0.000 description 1
- VUPDHIIPAKIKAB-UHFFFAOYSA-N 2,5-diphenylfuran Chemical compound C=1C=C(C=2C=CC=CC=2)OC=1C1=CC=CC=C1 VUPDHIIPAKIKAB-UHFFFAOYSA-N 0.000 description 1
- BOYLLHLMAHHGJB-UHFFFAOYSA-N 2,5-diphenylisoindole Chemical compound C1=CC2=CN(C=3C=CC=CC=3)C=C2C=C1C1=CC=CC=C1 BOYLLHLMAHHGJB-UHFFFAOYSA-N 0.000 description 1
- HWKZNRABKQDKTC-UHFFFAOYSA-N 2,5-diphenylthiophene Chemical compound C=1C=C(C=2C=CC=CC=2)SC=1C1=CC=CC=C1 HWKZNRABKQDKTC-UHFFFAOYSA-N 0.000 description 1
- MTUMHWPBSOBUCL-UHFFFAOYSA-N 2,6-dichloro-3-phenylpyridine Chemical compound ClC1=NC(Cl)=CC=C1C1=CC=CC=C1 MTUMHWPBSOBUCL-UHFFFAOYSA-N 0.000 description 1
- BWLDAWKGIGKTFJ-UHFFFAOYSA-N 2,6-dihydrazinylanthracene-9,10-dione Chemical compound NNC1=CC=C2C(=O)C3=CC(NN)=CC=C3C(=O)C2=C1 BWLDAWKGIGKTFJ-UHFFFAOYSA-N 0.000 description 1
- VVKGEJPRRZLPMT-AGFIODOGSA-N 2,6-dimethyl-3-[(e,7r,11r)-3,7,11,15-tetramethylhexadec-2-enyl]naphthalene-1,4-dione Chemical compound C1=C(C)C=C2C(=O)C(C/C=C(C)/CCC[C@H](C)CCC[C@H](C)CCCC(C)C)=C(C)C(=O)C2=C1 VVKGEJPRRZLPMT-AGFIODOGSA-N 0.000 description 1
- AQNQCHYHLXWGDR-UHFFFAOYSA-N 2,6-dimethyl-3-phenylnaphthalene-1,4-dione Chemical compound O=C1C2=CC(C)=CC=C2C(=O)C(C)=C1C1=CC=CC=C1 AQNQCHYHLXWGDR-UHFFFAOYSA-N 0.000 description 1
- QNRXYILTAFQFSQ-UHFFFAOYSA-N 2,6-diphenylpyrylium Chemical compound C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=[O+]1 QNRXYILTAFQFSQ-UHFFFAOYSA-N 0.000 description 1
- NHRLRCJZLMJELB-UHFFFAOYSA-N 2,8-diphenylpyrido[3,2-g]quinoline Chemical compound C1=CC=CC=C1C1=CC=C(C=C2C(N=C(C=C2)C=2C=CC=CC=2)=C2)C2=N1 NHRLRCJZLMJELB-UHFFFAOYSA-N 0.000 description 1
- QACOLYQTPFGDLC-UHFFFAOYSA-N 2-(1,3-oxazol-2-yl)aniline Chemical compound NC1=CC=CC=C1C1=NC=CO1 QACOLYQTPFGDLC-UHFFFAOYSA-N 0.000 description 1
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- JBRUZJYYBDYZSX-UHFFFAOYSA-N 2-(2-naphthalen-2-ylethyl)naphthalene Chemical compound C1=CC=CC2=CC(CCC=3C=C4C=CC=CC4=CC=3)=CC=C21 JBRUZJYYBDYZSX-UHFFFAOYSA-N 0.000 description 1
- BIEFDNUEROKZRA-UHFFFAOYSA-N 2-(2-phenylethenyl)aniline Chemical compound NC1=CC=CC=C1C=CC1=CC=CC=C1 BIEFDNUEROKZRA-UHFFFAOYSA-N 0.000 description 1
- XHBVYYMFLQGIJX-UHFFFAOYSA-N 2-(4-nitrophenyl)-1,3-oxazole Chemical compound C1=CC([N+](=O)[O-])=CC=C1C1=NC=CO1 XHBVYYMFLQGIJX-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- GBGPVUAOTCNZPT-UHFFFAOYSA-N 2-Methylcumarone Chemical compound C1=CC=C2OC(C)=CC2=C1 GBGPVUAOTCNZPT-UHFFFAOYSA-N 0.000 description 1
- FWLHAQYOFMQTHQ-UHFFFAOYSA-N 2-N-[8-[[8-(4-aminoanilino)-10-phenylphenazin-10-ium-2-yl]amino]-10-phenylphenazin-10-ium-2-yl]-8-N,10-diphenylphenazin-10-ium-2,8-diamine hydroxy-oxido-dioxochromium Chemical compound O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.Nc1ccc(Nc2ccc3nc4ccc(Nc5ccc6nc7ccc(Nc8ccc9nc%10ccc(Nc%11ccccc%11)cc%10[n+](-c%10ccccc%10)c9c8)cc7[n+](-c7ccccc7)c6c5)cc4[n+](-c4ccccc4)c3c2)cc1 FWLHAQYOFMQTHQ-UHFFFAOYSA-N 0.000 description 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- SAGXAQBTDLGHTF-UHFFFAOYSA-N 2-[(2,6-dihydroxyphenyl)diazenyl]-4-pyridin-4-ylbenzene-1,3-diol Chemical compound N1=CC=C(C=C1)C1=C(C(=C(O)C=C1)N=NC1=C(O)C=CC=C1O)O SAGXAQBTDLGHTF-UHFFFAOYSA-N 0.000 description 1
- PTWSIIUEOFZCHW-NTCAYCPXSA-N 2-[(2e)-3,7-dimethylocta-2,6-dienyl]-3-methylnaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CCC=C(C)C)=C(C)C(=O)C2=C1 PTWSIIUEOFZCHW-NTCAYCPXSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 1
- UDOGNMDURIJYQC-UHFFFAOYSA-N 2-amino-6-methyl-1h-pteridin-4-one Chemical compound N1C(N)=NC(=O)C2=NC(C)=CN=C21 UDOGNMDURIJYQC-UHFFFAOYSA-N 0.000 description 1
- RPLHSBWUCIUAGM-UHFFFAOYSA-N 2-aminoanthracen-1-ol Chemical compound C1=CC=CC2=CC3=C(O)C(N)=CC=C3C=C21 RPLHSBWUCIUAGM-UHFFFAOYSA-N 0.000 description 1
- ZUWGETJDHLRBSC-UHFFFAOYSA-N 2-anilino-3-bromonaphthalene-1,4-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C(Br)=C1NC1=CC=CC=C1 ZUWGETJDHLRBSC-UHFFFAOYSA-N 0.000 description 1
- ZFRMKMWVWYIEER-UHFFFAOYSA-N 2-anilino-3-phenylnaphthalene-1,4-dione Chemical compound C=1C=CC=CC=1C=1C(=O)C2=CC=CC=C2C(=O)C=1NC1=CC=CC=C1 ZFRMKMWVWYIEER-UHFFFAOYSA-N 0.000 description 1
- HCRMBUAINHNLEN-UHFFFAOYSA-N 2-azidoanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(N=[N+]=[N-])=CC=C3C(=O)C2=C1 HCRMBUAINHNLEN-UHFFFAOYSA-N 0.000 description 1
- UXGVMFHEKMGWMA-UHFFFAOYSA-N 2-benzofuran Chemical compound C1=CC=CC2=COC=C21 UXGVMFHEKMGWMA-UHFFFAOYSA-N 0.000 description 1
- LYTMVABTDYMBQK-UHFFFAOYSA-N 2-benzothiophene Chemical compound C1=CC=CC2=CSC=C21 LYTMVABTDYMBQK-UHFFFAOYSA-N 0.000 description 1
- XASGEXXLAQFTQE-UHFFFAOYSA-N 2-benzoylcyclohexa-2,5-diene-1,4-dione Chemical compound C=1C=CC=CC=1C(=O)C1=CC(=O)C=CC1=O XASGEXXLAQFTQE-UHFFFAOYSA-N 0.000 description 1
- FVKFNLCCKOHMFT-UHFFFAOYSA-N 2-benzoylxanthen-9-one Chemical compound C=1C=C2OC3=CC=CC=C3C(=O)C2=CC=1C(=O)C1=CC=CC=C1 FVKFNLCCKOHMFT-UHFFFAOYSA-N 0.000 description 1
- ZBVWBAAUURREBF-UHFFFAOYSA-N 2-benzyl-3-methylnaphthalene-1,4-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C(C)=C1CC1=CC=CC=C1 ZBVWBAAUURREBF-UHFFFAOYSA-N 0.000 description 1
- JASHTKAXQWIZGF-UHFFFAOYSA-N 2-benzylnaphthalene Chemical compound C=1C=C2C=CC=CC2=CC=1CC1=CC=CC=C1 JASHTKAXQWIZGF-UHFFFAOYSA-N 0.000 description 1
- QLQNUEHTRQBVTD-UHFFFAOYSA-N 2-bromo-5-phenyl-1h-imidazole Chemical compound N1C(Br)=NC=C1C1=CC=CC=C1 QLQNUEHTRQBVTD-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- YTAGJMFBUAHVDP-UHFFFAOYSA-N 2-chloro-6-phenylpyridine Chemical compound ClC1=CC=CC(C=2C=CC=CC=2)=N1 YTAGJMFBUAHVDP-UHFFFAOYSA-N 0.000 description 1
- NDAXYJIUSLEMIY-UHFFFAOYSA-N 2-chloroacridine Chemical compound C1=CC=CC2=CC3=CC(Cl)=CC=C3N=C21 NDAXYJIUSLEMIY-UHFFFAOYSA-N 0.000 description 1
- ZNJQWPJMTIZOHA-UHFFFAOYSA-N 2-chlorodibenzothiophene Chemical compound C1=CC=C2C3=CC(Cl)=CC=C3SC2=C1 ZNJQWPJMTIZOHA-UHFFFAOYSA-N 0.000 description 1
- SEUYUUNXDKEMLI-UHFFFAOYSA-N 2-chloroiminonaphthalen-1-one Chemical compound C1=CC=C2C(=O)C(=NCl)C=CC2=C1 SEUYUUNXDKEMLI-UHFFFAOYSA-N 0.000 description 1
- OFUFXTHGZWIDDB-UHFFFAOYSA-N 2-chloroquinoline Chemical compound C1=CC=CC2=NC(Cl)=CC=C21 OFUFXTHGZWIDDB-UHFFFAOYSA-N 0.000 description 1
- GNUGVECARVKIPH-UHFFFAOYSA-N 2-ethenoxypropane Chemical compound CC(C)OC=C GNUGVECARVKIPH-UHFFFAOYSA-N 0.000 description 1
- YGIJVERMYRLOTF-UHFFFAOYSA-N 2-ethenyl-2-methyl-1h-pyridine Chemical compound C=CC1(C)NC=CC=C1 YGIJVERMYRLOTF-UHFFFAOYSA-N 0.000 description 1
- SEAQTGXUOXUPQN-UHFFFAOYSA-N 2-ethenyl-4,6-dimethyl-1,3,5-triazine Chemical compound CC1=NC(C)=NC(C=C)=N1 SEAQTGXUOXUPQN-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- TZYRSLHNPKPEFV-UHFFFAOYSA-N 2-ethyl-1-butanol Chemical compound CCC(CC)CO TZYRSLHNPKPEFV-UHFFFAOYSA-N 0.000 description 1
- RLAASDPFGKXAIY-UHFFFAOYSA-N 2-ethyl-1-methylphenanthrene Chemical compound C1=CC=C2C3=CC=C(CC)C(C)=C3C=CC2=C1 RLAASDPFGKXAIY-UHFFFAOYSA-N 0.000 description 1
- SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 description 1
- CHNGPLVDGWOPMD-UHFFFAOYSA-N 2-ethylbutyl 2-methylprop-2-enoate Chemical compound CCC(CC)COC(=O)C(C)=C CHNGPLVDGWOPMD-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- XCIZVKSCLVSDHN-UHFFFAOYSA-N 2-ethylquinoline Chemical compound C1=CC=CC2=NC(CC)=CC=C21 XCIZVKSCLVSDHN-UHFFFAOYSA-N 0.000 description 1
- NLEPLDKPYLYCSY-UHFFFAOYSA-N 2-fluoroquinoline Chemical compound C1=CC=CC2=NC(F)=CC=C21 NLEPLDKPYLYCSY-UHFFFAOYSA-N 0.000 description 1
- IEYTYHPAPAAGCS-UHFFFAOYSA-N 2-iodonaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(I)=CC(=O)C2=C1 IEYTYHPAPAAGCS-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- BYVDYBMDKJLNFV-UHFFFAOYSA-N 2-methyl-1,3-diphenylisoindole Chemical compound C=12C=CC=CC2=C(C=2C=CC=CC=2)N(C)C=1C1=CC=CC=C1 BYVDYBMDKJLNFV-UHFFFAOYSA-N 0.000 description 1
- FZJUONUBFWNHNU-UHFFFAOYSA-N 2-methyl-1-oxidoquinolin-1-ium Chemical compound C1=CC=CC2=[N+]([O-])C(C)=CC=C21 FZJUONUBFWNHNU-UHFFFAOYSA-N 0.000 description 1
- WWXBHJICFDGVQR-UHFFFAOYSA-N 2-methyl-1-phenylpyrrole Chemical compound CC1=CC=CN1C1=CC=CC=C1 WWXBHJICFDGVQR-UHFFFAOYSA-N 0.000 description 1
- RCQDLJXVQRWEON-UHFFFAOYSA-N 2-methyl-3-(3,7,11-trimethyldodeca-2,6,10-trienyl)naphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(CC=C(C)CCC=C(C)CCC=C(C)C)=C(C)C(=O)C2=C1 RCQDLJXVQRWEON-UHFFFAOYSA-N 0.000 description 1
- LPXDOYLEJMCQJO-UHFFFAOYSA-N 2-methyl-3-(3-phenylprop-2-enyl)naphthalene-1,4-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C(C)=C1CC=CC1=CC=CC=C1 LPXDOYLEJMCQJO-UHFFFAOYSA-N 0.000 description 1
- RPTYBOWTTKHRKG-UHFFFAOYSA-N 2-methyl-3-trityl-1h-indole Chemical compound CC=1NC2=CC=CC=C2C=1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 RPTYBOWTTKHRKG-UHFFFAOYSA-N 0.000 description 1
- JSTFROSQSCXFPA-UHFFFAOYSA-N 2-methyl-3h-1,2-thiazole Chemical compound CN1CC=CS1 JSTFROSQSCXFPA-UHFFFAOYSA-N 0.000 description 1
- QLQIWRCWPJRJJA-UHFFFAOYSA-N 2-methyl-4,5-diphenyl-1,3-oxazole Chemical compound O1C(C)=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 QLQIWRCWPJRJJA-UHFFFAOYSA-N 0.000 description 1
- ZFYWCVZNRMSXBT-UHFFFAOYSA-N 2-methyl-4,5-diphenyl-1,3-thiazole Chemical compound S1C(C)=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 ZFYWCVZNRMSXBT-UHFFFAOYSA-N 0.000 description 1
- FGTSBVMVXJRFBS-UHFFFAOYSA-N 2-methyl-4-phenyl-1,3-oxazole Chemical compound O1C(C)=NC(C=2C=CC=CC=2)=C1 FGTSBVMVXJRFBS-UHFFFAOYSA-N 0.000 description 1
- XROORURTAQOYLW-UHFFFAOYSA-N 2-methyl-4-phenyl-1,3-thiazole Chemical compound S1C(C)=NC(C=2C=CC=CC=2)=C1 XROORURTAQOYLW-UHFFFAOYSA-N 0.000 description 1
- WEEKSQBGSMJFMW-UHFFFAOYSA-N 2-methyl-4-phenyl-1h-pyrrole Chemical compound N1C(C)=CC(C=2C=CC=CC=2)=C1 WEEKSQBGSMJFMW-UHFFFAOYSA-N 0.000 description 1
- MBXIOFXLAGTBGI-UHFFFAOYSA-N 2-methyl-4-phenylquinoline Chemical compound C=12C=CC=CC2=NC(C)=CC=1C1=CC=CC=C1 MBXIOFXLAGTBGI-UHFFFAOYSA-N 0.000 description 1
- PXBSHTWLLVDXIH-UHFFFAOYSA-N 2-methyl-5-phenyl-1,3-oxazole Chemical compound O1C(C)=NC=C1C1=CC=CC=C1 PXBSHTWLLVDXIH-UHFFFAOYSA-N 0.000 description 1
- LOLZVJJIBIGCFD-UHFFFAOYSA-N 2-methyl-5-phenyl-1h-pyrrole Chemical compound N1C(C)=CC=C1C1=CC=CC=C1 LOLZVJJIBIGCFD-UHFFFAOYSA-N 0.000 description 1
- WONYVCKUEUULQN-UHFFFAOYSA-N 2-methyl-n-(2-methylphenyl)aniline Chemical compound CC1=CC=CC=C1NC1=CC=CC=C1C WONYVCKUEUULQN-UHFFFAOYSA-N 0.000 description 1
- JTMODJXOTWYBOZ-UHFFFAOYSA-N 2-methyl-n-phenylaniline Chemical compound CC1=CC=CC=C1NC1=CC=CC=C1 JTMODJXOTWYBOZ-UHFFFAOYSA-N 0.000 description 1
- JPKKMFOXWKNEEN-UHFFFAOYSA-N 2-methylcholine Chemical compound CC(O)C[N+](C)(C)C JPKKMFOXWKNEEN-UHFFFAOYSA-N 0.000 description 1
- WIAZTPUQHUFMQA-UHFFFAOYSA-N 2-methylnaphthalene-1-carbaldehyde Chemical compound C1=CC=CC2=C(C=O)C(C)=CC=C21 WIAZTPUQHUFMQA-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- AFKSITGTMMVRQX-UHFFFAOYSA-N 2-methylsulfonyl-5-phenyl-1,3,4-thiadiazole Chemical compound S1C(S(=O)(=O)C)=NN=C1C1=CC=CC=C1 AFKSITGTMMVRQX-UHFFFAOYSA-N 0.000 description 1
- MNUUAKJFDJVFQI-UHFFFAOYSA-N 2-naphthalen-1-yl-2-oxoacetaldehyde Chemical compound C1=CC=C2C(C(=O)C=O)=CC=CC2=C1 MNUUAKJFDJVFQI-UHFFFAOYSA-N 0.000 description 1
- GVQSKNGMWJDYSQ-UHFFFAOYSA-N 2-naphthalen-1-yl-3-trityl-1h-indole Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=C(C=2C3=CC=CC=C3C=CC=2)NC2=CC=CC=C12 GVQSKNGMWJDYSQ-UHFFFAOYSA-N 0.000 description 1
- OQRMWUNUKVUHQO-UHFFFAOYSA-N 2-naphthalen-1-ylacetonitrile Chemical compound C1=CC=C2C(CC#N)=CC=CC2=C1 OQRMWUNUKVUHQO-UHFFFAOYSA-N 0.000 description 1
- IBENYRAUOZMVRG-UHFFFAOYSA-N 2-naphthalen-1-ylpropan-2-ol Chemical compound C1=CC=C2C(C(C)(O)C)=CC=CC2=C1 IBENYRAUOZMVRG-UHFFFAOYSA-N 0.000 description 1
- FDZMEYJSJZWIEJ-UHFFFAOYSA-N 2-naphthalen-2-yl-2-oxoacetaldehyde Chemical compound C1=CC=CC2=CC(C(=O)C=O)=CC=C21 FDZMEYJSJZWIEJ-UHFFFAOYSA-N 0.000 description 1
- CSONNHKIVVSLQQ-UHFFFAOYSA-N 2-naphthalen-2-ylpropan-2-ol Chemical compound C1=CC=CC2=CC(C(C)(O)C)=CC=C21 CSONNHKIVVSLQQ-UHFFFAOYSA-N 0.000 description 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 1
- JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 1
- VGXDTOMHQFSMGM-UHFFFAOYSA-N 2-nitro-1-phenylnaphthalene Chemical compound [O-][N+](=O)C1=CC=C2C=CC=CC2=C1C1=CC=CC=C1 VGXDTOMHQFSMGM-UHFFFAOYSA-N 0.000 description 1
- GXLYVLHWXVRVKI-UHFFFAOYSA-N 2-nitrodibenzothiophene Chemical compound C1=CC=C2C3=CC([N+](=O)[O-])=CC=C3SC2=C1 GXLYVLHWXVRVKI-UHFFFAOYSA-N 0.000 description 1
- PIAOLBVUVDXHHL-UHFFFAOYSA-N 2-nitroethenylbenzene Chemical compound [O-][N+](=O)C=CC1=CC=CC=C1 PIAOLBVUVDXHHL-UHFFFAOYSA-N 0.000 description 1
- UDAIGHZFMLGNDQ-UHFFFAOYSA-N 2-nitroquinoline Chemical compound C1=CC=CC2=NC([N+](=O)[O-])=CC=C21 UDAIGHZFMLGNDQ-UHFFFAOYSA-N 0.000 description 1
- FOZRXNFKVJZBPI-UHFFFAOYSA-N 2-oxido-3-phenyl-1,2,5-oxadiazol-2-ium Chemical compound O1N=CC(C=2C=CC=CC=2)=[N+]1[O-] FOZRXNFKVJZBPI-UHFFFAOYSA-N 0.000 description 1
- MCHGPIKQVQBUMX-UHFFFAOYSA-N 2-oxo-1h-naphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(C=O)C(=O)C=CC2=C1 MCHGPIKQVQBUMX-UHFFFAOYSA-N 0.000 description 1
- ZMJRUUBDMPKHJS-UHFFFAOYSA-N 2-phenyl-1,3,4-thiadiazole Chemical compound S1C=NN=C1C1=CC=CC=C1 ZMJRUUBDMPKHJS-UHFFFAOYSA-N 0.000 description 1
- XBHOUXSGHYZCNH-UHFFFAOYSA-N 2-phenyl-1,3-benzothiazole Chemical compound C1=CC=CC=C1C1=NC2=CC=CC=C2S1 XBHOUXSGHYZCNH-UHFFFAOYSA-N 0.000 description 1
- RQCBPOPQTLHDFC-UHFFFAOYSA-N 2-phenyl-1,3-oxazole Chemical compound C1=COC(C=2C=CC=CC=2)=N1 RQCBPOPQTLHDFC-UHFFFAOYSA-N 0.000 description 1
- AXEWHCCRSVCUKW-UHFFFAOYSA-N 2-phenyl-1h-benzo[e][1,2]benzothiazole Chemical compound S1C2=CC=C3C=CC=CC3=C2CN1C1=CC=CC=C1 AXEWHCCRSVCUKW-UHFFFAOYSA-N 0.000 description 1
- ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 description 1
- AJHQOVPQWVDPEJ-UHFFFAOYSA-N 2-phenyl-3-trityl-1h-indole Chemical compound C1=CC=CC=C1C1=C(C(C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)C2=CC=CC=C2N1 AJHQOVPQWVDPEJ-UHFFFAOYSA-N 0.000 description 1
- UDHQYCHTORTPRF-UHFFFAOYSA-N 2-phenylcyclohepta-2,4,6-trien-1-one Chemical compound O=C1C=CC=CC=C1C1=CC=CC=C1 UDHQYCHTORTPRF-UHFFFAOYSA-N 0.000 description 1
- XJCQBQWPASYUHR-UHFFFAOYSA-N 2-phenylcyclohexa-2,4-diene-1,1-diamine Chemical group NC1(N)CC=CC=C1C1=CC=CC=C1 XJCQBQWPASYUHR-UHFFFAOYSA-N 0.000 description 1
- GCXNJAXHHFZVIM-UHFFFAOYSA-N 2-phenylfuran Chemical compound C1=COC(C=2C=CC=CC=2)=C1 GCXNJAXHHFZVIM-UHFFFAOYSA-N 0.000 description 1
- IXOZZKPZLXAEAX-UHFFFAOYSA-N 2-phenylindazole Chemical compound N1=C2C=CC=CC2=CN1C1=CC=CC=C1 IXOZZKPZLXAEAX-UHFFFAOYSA-N 0.000 description 1
- CUZKCNWZBXLAJX-UHFFFAOYSA-N 2-phenylmethoxyethanol Chemical compound OCCOCC1=CC=CC=C1 CUZKCNWZBXLAJX-UHFFFAOYSA-N 0.000 description 1
- CIDYIYSNDAJNGX-UHFFFAOYSA-N 2-phenylnaphthalene-1,4-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 CIDYIYSNDAJNGX-UHFFFAOYSA-N 0.000 description 1
- QKCKCXFWENOGER-UHFFFAOYSA-N 2-phenyloxazol-5(4H)-one Chemical compound O1C(=O)CN=C1C1=CC=CC=C1 QKCKCXFWENOGER-UHFFFAOYSA-N 0.000 description 1
- PJRGDKFLFAYRBV-UHFFFAOYSA-N 2-phenylthiophene Chemical compound C1=CSC(C=2C=CC=CC=2)=C1 PJRGDKFLFAYRBV-UHFFFAOYSA-N 0.000 description 1
- JYBWAYHAOLQZJX-UHFFFAOYSA-N 2-phenyltriazole Chemical compound N1=CC=NN1C1=CC=CC=C1 JYBWAYHAOLQZJX-UHFFFAOYSA-N 0.000 description 1
- HCGFUIQPSOCUHI-UHFFFAOYSA-N 2-propan-2-yloxyethanol Chemical compound CC(C)OCCO HCGFUIQPSOCUHI-UHFFFAOYSA-N 0.000 description 1
- KXYAVSFOJVUIHT-UHFFFAOYSA-N 2-vinylnaphthalene Chemical compound C1=CC=CC2=CC(C=C)=CC=C21 KXYAVSFOJVUIHT-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- BBKZDKYIYIIMKE-UHFFFAOYSA-N 2h-1,2,3-benzotriazin-3-amine Chemical compound C1=CC=CC2=CN(N)NN=C21 BBKZDKYIYIIMKE-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
- QNXWBZYCPMWRPF-UHFFFAOYSA-N 3,10-dinitroperylene Chemical group C=12C3=CC=C([N+]([O-])=O)C2=CC=CC=1C1=CC=CC2=C1C3=CC=C2[N+](=O)[O-] QNXWBZYCPMWRPF-UHFFFAOYSA-N 0.000 description 1
- ZVOMKZHDZNGXPN-UHFFFAOYSA-N 3,4,5-triphenyl-1,2-oxazole Chemical compound C1=CC=CC=C1C1=NOC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 ZVOMKZHDZNGXPN-UHFFFAOYSA-N 0.000 description 1
- FZLPJLFDDSLQOB-UHFFFAOYSA-N 3,4-dichloronaphtho[2,3-h]cinnoline Chemical compound C1=CC=C2C=C3C4=NN=C(Cl)C(Cl)=C4C=CC3=CC2=C1 FZLPJLFDDSLQOB-UHFFFAOYSA-N 0.000 description 1
- SEBPXHSZHLFWRL-UHFFFAOYSA-N 3,4-dihydro-2,2,5,7,8-pentamethyl-2h-1-benzopyran-6-ol Chemical compound O1C(C)(C)CCC2=C1C(C)=C(C)C(O)=C2C SEBPXHSZHLFWRL-UHFFFAOYSA-N 0.000 description 1
- OSBWKHOBLYJAEW-UHFFFAOYSA-N 3,4-dihydro-2h-naphthalene-1,1-diamine Chemical compound C1=CC=C2C(N)(N)CCCC2=C1 OSBWKHOBLYJAEW-UHFFFAOYSA-N 0.000 description 1
- RIIIXRZGXAJVEQ-UHFFFAOYSA-N 3,4-diphenyl-1,2,5-oxadiazole Chemical compound C1=CC=CC=C1C1=NON=C1C1=CC=CC=C1 RIIIXRZGXAJVEQ-UHFFFAOYSA-N 0.000 description 1
- KFGFVPMRLOQXNB-UHFFFAOYSA-N 3,5,5-trimethylhexanoyl 3,5,5-trimethylhexaneperoxoate Chemical compound CC(C)(C)CC(C)CC(=O)OOC(=O)CC(C)CC(C)(C)C KFGFVPMRLOQXNB-UHFFFAOYSA-N 0.000 description 1
- ULPBJGVRVXWECP-UHFFFAOYSA-N 3,5-dimethyl-1-(4-nitrophenyl)pyrazole Chemical compound N1=C(C)C=C(C)N1C1=CC=C([N+]([O-])=O)C=C1 ULPBJGVRVXWECP-UHFFFAOYSA-N 0.000 description 1
- FARDGLNBVDMFLZ-UHFFFAOYSA-N 3,6-diaminophenanthrene-1,2-dione Chemical compound C1=C(N)C=C2C(C=C(C(C3=O)=O)N)=C3C=CC2=C1 FARDGLNBVDMFLZ-UHFFFAOYSA-N 0.000 description 1
- YAILYEMDUBVLNS-UHFFFAOYSA-N 3,6-diphenyl-1h-pyrazin-2-one Chemical compound O=C1NC(C=2C=CC=CC=2)=CN=C1C1=CC=CC=C1 YAILYEMDUBVLNS-UHFFFAOYSA-N 0.000 description 1
- HQOCJWXUUAJSMJ-UHFFFAOYSA-N 3,9-diphenyl-9h-xanthene Chemical compound C12=CC=C(C=3C=CC=CC=3)C=C2OC2=CC=CC=C2C1C1=CC=CC=C1 HQOCJWXUUAJSMJ-UHFFFAOYSA-N 0.000 description 1
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 1
- XDXBQTMZTULWMV-UHFFFAOYSA-N 3-(2-nitrophenyl)-1h-indole Chemical compound [O-][N+](=O)C1=CC=CC=C1C1=CNC2=CC=CC=C12 XDXBQTMZTULWMV-UHFFFAOYSA-N 0.000 description 1
- AXSPMUDWTDIMLH-UHFFFAOYSA-N 3-(bromomethyl)isoquinoline Chemical compound C1=CC=C2C=NC(CBr)=CC2=C1 AXSPMUDWTDIMLH-UHFFFAOYSA-N 0.000 description 1
- PIIQLZXRLGJEKE-LSDHHAIUSA-N 3-[(3r,4r)-3-ethenylpiperidin-4-yl]-1-quinolin-4-ylpropan-1-one Chemical compound C=C[C@H]1CNCC[C@H]1CCC(=O)C1=CC=NC2=CC=CC=C12 PIIQLZXRLGJEKE-LSDHHAIUSA-N 0.000 description 1
- LBBAKTMYSIFTBS-UHFFFAOYSA-N 3-[(4-aminophenyl)diazenyl]benzene-1,2-diamine Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC(N)=C1N LBBAKTMYSIFTBS-UHFFFAOYSA-N 0.000 description 1
- YNSCKPCDFIDINW-UHFFFAOYSA-N 3-[[2-[[1-[2-(dimethylamino)acetyl]-6-methoxy-4,4-dimethyl-2,3-dihydroquinolin-7-yl]amino]-7h-pyrrolo[2,3-d]pyrimidin-4-yl]amino]thiophene-2-carboxamide Chemical compound COC1=CC(C(CCN2C(=O)CN(C)C)(C)C)=C2C=C1NC(N=C1NC=CC1=1)=NC=1NC=1C=CSC=1C(N)=O YNSCKPCDFIDINW-UHFFFAOYSA-N 0.000 description 1
- CKSHWZXSTMVBAG-UHFFFAOYSA-N 3-benzoyl-6-chloro-2-phenylchromen-4-one Chemical compound C=1C=CC=CC=1C(=O)C=1C(=O)C2=CC(Cl)=CC=C2OC=1C1=CC=CC=C1 CKSHWZXSTMVBAG-UHFFFAOYSA-N 0.000 description 1
- ZGIKWINFUGEQEO-UHFFFAOYSA-N 3-bromoquinoline Chemical compound C1=CC=CC2=CC(Br)=CN=C21 ZGIKWINFUGEQEO-UHFFFAOYSA-N 0.000 description 1
- UFIGOYSEDNHKGT-UHFFFAOYSA-N 3-fluoroquinoline Chemical compound C1=CC=CC2=CC(F)=CN=C21 UFIGOYSEDNHKGT-UHFFFAOYSA-N 0.000 description 1
- LWFKFPKCTLFBCB-UHFFFAOYSA-N 3-imino-2-phenylchromen-4-one Chemical compound O1C2=CC=CC=C2C(=O)C(=N)C1C1=CC=CC=C1 LWFKFPKCTLFBCB-UHFFFAOYSA-N 0.000 description 1
- FTULWSIJOKUBOV-UHFFFAOYSA-N 3-methoxy-4-(2-methoxybut-3-enoxy)but-1-ene Chemical compound COC(C=C)COCC(OC)C=C FTULWSIJOKUBOV-UHFFFAOYSA-N 0.000 description 1
- ZOOFOAYUIMNTDZ-UHFFFAOYSA-N 3-methyl-2,4-diphenylfuran Chemical compound CC=1C(C=2C=CC=CC=2)=COC=1C1=CC=CC=C1 ZOOFOAYUIMNTDZ-UHFFFAOYSA-N 0.000 description 1
- ZCTBUBMRXYVEHX-UHFFFAOYSA-N 3-methyl-4-phenyl-1,2-oxazol-5-amine Chemical compound CC1=NOC(N)=C1C1=CC=CC=C1 ZCTBUBMRXYVEHX-UHFFFAOYSA-N 0.000 description 1
- ZTWRWSTUMWZTAU-UHFFFAOYSA-N 3-methyl-5-phenyl-1,2,4-oxadiazole Chemical compound CC1=NOC(C=2C=CC=CC=2)=N1 ZTWRWSTUMWZTAU-UHFFFAOYSA-N 0.000 description 1
- CEYRROMZZGLFSL-UHFFFAOYSA-N 3-methylcinnoline Chemical compound C1=CC=C2N=NC(C)=CC2=C1 CEYRROMZZGLFSL-UHFFFAOYSA-N 0.000 description 1
- BJPNADFNSANIPF-UHFFFAOYSA-N 3-methylquinoxaline-2-carboxylic acid Chemical compound C1=CC=C2N=C(C(O)=O)C(C)=NC2=C1 BJPNADFNSANIPF-UHFFFAOYSA-N 0.000 description 1
- CMJXSNIHVCVAEZ-UHFFFAOYSA-N 3-n-pyridin-3-ylbenzene-1,3-diamine Chemical compound NC1=CC=CC(NC=2C=NC=CC=2)=C1 CMJXSNIHVCVAEZ-UHFFFAOYSA-N 0.000 description 1
- VVUXXNFYPNKDJY-UHFFFAOYSA-N 3-n-pyridin-4-ylbenzene-1,3-diamine Chemical compound NC1=CC=CC(NC=2C=CN=CC=2)=C1 VVUXXNFYPNKDJY-UHFFFAOYSA-N 0.000 description 1
- ZXVRNZRQQRBDLX-UHFFFAOYSA-N 3-nitroquinoline Chemical compound C1=CC=CC2=CC([N+](=O)[O-])=CN=C21 ZXVRNZRQQRBDLX-UHFFFAOYSA-N 0.000 description 1
- WYVBOPZYVJIBSW-UHFFFAOYSA-N 3-oxido-4-phenyl-1,2,3-benzotriazin-3-ium Chemical compound [O-][N+]1=NN=C2C=CC=CC2=C1C1=CC=CC=C1 WYVBOPZYVJIBSW-UHFFFAOYSA-N 0.000 description 1
- CHJJHGSNNPEDNJ-UHFFFAOYSA-N 3-phenyl-1,2,5-oxadiazole Chemical compound C1=NON=C1C1=CC=CC=C1 CHJJHGSNNPEDNJ-UHFFFAOYSA-N 0.000 description 1
- SSYBGLWXGRWEFE-UHFFFAOYSA-N 3-phenyl-1-benzofuran Chemical compound C=1OC2=CC=CC=C2C=1C1=CC=CC=C1 SSYBGLWXGRWEFE-UHFFFAOYSA-N 0.000 description 1
- MXBKCOLSUUYOHT-UHFFFAOYSA-N 3-phenyl-1h-indazole Chemical compound C1=CC=CC=C1C1=NNC2=CC=CC=C12 MXBKCOLSUUYOHT-UHFFFAOYSA-N 0.000 description 1
- ORXSOQFSAQHWSR-UHFFFAOYSA-N 3-phenyl-1h-quinolin-2-one Chemical compound O=C1NC2=CC=CC=C2C=C1C1=CC=CC=C1 ORXSOQFSAQHWSR-UHFFFAOYSA-N 0.000 description 1
- REGAHGRRCZCIDN-UHFFFAOYSA-N 3-trityl-1h-indole Chemical compound C=1NC2=CC=CC=C2C=1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 REGAHGRRCZCIDN-UHFFFAOYSA-N 0.000 description 1
- UNTNRNUQVKDIPV-UHFFFAOYSA-N 3h-dithiazole Chemical compound N1SSC=C1 UNTNRNUQVKDIPV-UHFFFAOYSA-N 0.000 description 1
- OGRBAJCMDMEFIB-UHFFFAOYSA-N 4,4-dinitro-2,3-dihydro-1h-naphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])([N+]([O-])=O)CCCC2=C1 OGRBAJCMDMEFIB-UHFFFAOYSA-N 0.000 description 1
- PUYRDPWAITXGOH-UHFFFAOYSA-N 4,5-bis(bromomethyl)phenanthrene Chemical compound C1=CC=C(CBr)C2=C3C(CBr)=CC=CC3=CC=C21 PUYRDPWAITXGOH-UHFFFAOYSA-N 0.000 description 1
- WPEBMUGUTWAODF-UHFFFAOYSA-N 4,5-dimethyl-2-phenyl-1,3-oxazole Chemical compound O1C(C)=C(C)N=C1C1=CC=CC=C1 WPEBMUGUTWAODF-UHFFFAOYSA-N 0.000 description 1
- OQVKZPBAFRTWEE-UHFFFAOYSA-N 4,5-dimethyl-2-phenyl-3H-1,3-oxazol-2-ol Chemical compound N1C(C)=C(C)OC1(O)C1=CC=CC=C1 OQVKZPBAFRTWEE-UHFFFAOYSA-N 0.000 description 1
- HEBQNHXMMOMBII-UHFFFAOYSA-N 4,5-dinitro-3-phenyl-1h-indazole Chemical compound C12=C([N+]([O-])=O)C([N+](=O)[O-])=CC=C2NN=C1C1=CC=CC=C1 HEBQNHXMMOMBII-UHFFFAOYSA-N 0.000 description 1
- BGTVICKPWACXLR-UHFFFAOYSA-N 4,5-diphenyl-1,3-thiazole Chemical compound S1C=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 BGTVICKPWACXLR-UHFFFAOYSA-N 0.000 description 1
- CPHGOBGXZQKCKI-UHFFFAOYSA-N 4,5-diphenyl-1h-imidazole Chemical compound N1C=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 CPHGOBGXZQKCKI-UHFFFAOYSA-N 0.000 description 1
- TVNUWBFICZWTRU-UHFFFAOYSA-N 4,6-dimethyl-2-phenylpyrimidine Chemical compound CC1=CC(C)=NC(C=2C=CC=CC=2)=N1 TVNUWBFICZWTRU-UHFFFAOYSA-N 0.000 description 1
- DNQSBSBAVKNFBM-UHFFFAOYSA-N 4,7-phenanthrolin-5-amine Chemical compound C1=CN=C2C(N)=CC3=NC=CC=C3C2=C1 DNQSBSBAVKNFBM-UHFFFAOYSA-N 0.000 description 1
- SLLOVNWUCAZDJC-UHFFFAOYSA-N 4-(1,3-oxazol-2-yl)aniline Chemical compound C1=CC(N)=CC=C1C1=NC=CO1 SLLOVNWUCAZDJC-UHFFFAOYSA-N 0.000 description 1
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 1
- VYRRJMIFTUWRBX-UHFFFAOYSA-N 4-aminophenanthren-1-ol Chemical compound C1=CC=CC2=C3C(N)=CC=C(O)C3=CC=C21 VYRRJMIFTUWRBX-UHFFFAOYSA-N 0.000 description 1
- JRHBDYVANXBNPZ-UHFFFAOYSA-N 4-benzhydrylbenzaldehyde Chemical compound C1=CC(C=O)=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 JRHBDYVANXBNPZ-UHFFFAOYSA-N 0.000 description 1
- FCEWTGMJFIDTPT-UHFFFAOYSA-N 4-benzhydrylnaphthalene-1,2-dione Chemical compound C12=CC=CC=C2C(=O)C(=O)C=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 FCEWTGMJFIDTPT-UHFFFAOYSA-N 0.000 description 1
- HWRXVMYFKGLIJE-UHFFFAOYSA-N 4-benzoylcyclohexa-2,4-dien-1-one Chemical compound C=1C=CC=CC=1C(=O)C1=CCC(=O)C=C1 HWRXVMYFKGLIJE-UHFFFAOYSA-N 0.000 description 1
- SESASPRCAIMYLA-UHFFFAOYSA-N 4-bromonaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(Br)=CC=C(C=O)C2=C1 SESASPRCAIMYLA-UHFFFAOYSA-N 0.000 description 1
- XLKQQTZNAXAKFP-UHFFFAOYSA-N 4-chloro-1,2-dihydronaphthalene Chemical compound C1=CC=C2C(Cl)=CCCC2=C1 XLKQQTZNAXAKFP-UHFFFAOYSA-N 0.000 description 1
- IJSFFUOWXQRDMS-UHFFFAOYSA-N 4-chlorocinnoline Chemical compound C1=CC=C2C(Cl)=CN=NC2=C1 IJSFFUOWXQRDMS-UHFFFAOYSA-N 0.000 description 1
- GVRRXASZZAKBMN-UHFFFAOYSA-N 4-chloroquinazoline Chemical compound C1=CC=C2C(Cl)=NC=NC2=C1 GVRRXASZZAKBMN-UHFFFAOYSA-N 0.000 description 1
- KNDOFJFSHZCKGT-UHFFFAOYSA-N 4-chloroquinoline Chemical compound C1=CC=C2C(Cl)=CC=NC2=C1 KNDOFJFSHZCKGT-UHFFFAOYSA-N 0.000 description 1
- APQGUVGBMIKOFN-UHFFFAOYSA-N 4-ethyl-2-phenylphthalazin-1-one Chemical compound O=C1C2=CC=CC=C2C(CC)=NN1C1=CC=CC=C1 APQGUVGBMIKOFN-UHFFFAOYSA-N 0.000 description 1
- LVSQXDHWDCMMRJ-UHFFFAOYSA-N 4-hydroxybutan-2-one Chemical compound CC(=O)CCO LVSQXDHWDCMMRJ-UHFFFAOYSA-N 0.000 description 1
- MVXMNHYVCLMLDD-UHFFFAOYSA-N 4-methoxynaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(OC)=CC=C(C=O)C2=C1 MVXMNHYVCLMLDD-UHFFFAOYSA-N 0.000 description 1
- PVNJFQGMFSSSFS-UHFFFAOYSA-N 4-methyl-2,5-diphenyl-3H-1,3-oxazol-2-ol Chemical compound N1C(C)=C(C=2C=CC=CC=2)OC1(O)C1=CC=CC=C1 PVNJFQGMFSSSFS-UHFFFAOYSA-N 0.000 description 1
- HDJXQTMAHXKBJP-UHFFFAOYSA-N 4-methyl-2-[4-(4-methyl-1,3-thiazol-2-yl)phenyl]-1,3-thiazole Chemical compound CC1=CSC(C=2C=CC(=CC=2)C=2SC=C(C)N=2)=N1 HDJXQTMAHXKBJP-UHFFFAOYSA-N 0.000 description 1
- KIDJISUVJMVGAN-UHFFFAOYSA-N 4-methyl-2-phenyl-1,3-oxazole Chemical compound CC1=COC(C=2C=CC=CC=2)=N1 KIDJISUVJMVGAN-UHFFFAOYSA-N 0.000 description 1
- IPOHWQDCODUHTD-UHFFFAOYSA-N 4-methyl-2-phenyl-1,3-thiazole Chemical compound CC1=CSC(C=2C=CC=CC=2)=N1 IPOHWQDCODUHTD-UHFFFAOYSA-N 0.000 description 1
- YIAAMAHGPLMCJP-UHFFFAOYSA-N 4-methyl-2-phenyl-1h-pyrrole Chemical compound CC1=CNC(C=2C=CC=CC=2)=C1 YIAAMAHGPLMCJP-UHFFFAOYSA-N 0.000 description 1
- LQPDCTIPWIJXCR-UHFFFAOYSA-N 4-methyl-3-phenylchromen-2-one Chemical compound O=C1OC=2C=CC=CC=2C(C)=C1C1=CC=CC=C1 LQPDCTIPWIJXCR-UHFFFAOYSA-N 0.000 description 1
- GJNOITCBWGUZLQ-UHFFFAOYSA-N 4-methyl-3H-chromene-2,5,7-trione Chemical compound O=C1C2=C(CC(OC2=CC(C1)=O)=O)C GJNOITCBWGUZLQ-UHFFFAOYSA-N 0.000 description 1
- DNHKSCAYDWTXHD-UHFFFAOYSA-N 4-methyl-5-phenyl-1,3-thiazole Chemical compound N1=CSC(C=2C=CC=CC=2)=C1C DNHKSCAYDWTXHD-UHFFFAOYSA-N 0.000 description 1
- PQEOPHYIUYAVDQ-UHFFFAOYSA-N 4-methyl-n-phenylbenzamide Chemical compound C1=CC(C)=CC=C1C(=O)NC1=CC=CC=C1 PQEOPHYIUYAVDQ-UHFFFAOYSA-N 0.000 description 1
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 1
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 description 1
- UTMDJGPRCLQPBT-UHFFFAOYSA-N 4-nitro-1h-1,2,3-benzotriazole Chemical compound [O-][N+](=O)C1=CC=CC2=NNN=C12 UTMDJGPRCLQPBT-UHFFFAOYSA-N 0.000 description 1
- FQEPRUKGWGZQFA-UHFFFAOYSA-N 4-nitronaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=C(C=O)C2=C1 FQEPRUKGWGZQFA-UHFFFAOYSA-N 0.000 description 1
- ZPVSFHWMXABGPU-UHFFFAOYSA-N 4-nitroquinoline Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=NC2=C1 ZPVSFHWMXABGPU-UHFFFAOYSA-N 0.000 description 1
- JCEXBUYUHYXFME-UHFFFAOYSA-N 4-nitrosonaphthalen-1-amine Chemical compound C1=CC=C2C(N)=CC=C(N=O)C2=C1 JCEXBUYUHYXFME-UHFFFAOYSA-N 0.000 description 1
- ZVNOVIBCAIDQOE-UHFFFAOYSA-N 4-nitrosonaphthalen-1-ol Chemical compound C1=CC=C2C(O)=CC=C(N=O)C2=C1 ZVNOVIBCAIDQOE-UHFFFAOYSA-N 0.000 description 1
- NTFMLYSGIKHECT-UHFFFAOYSA-N 4-phenyl-1,3-oxazole Chemical compound O1C=NC(C=2C=CC=CC=2)=C1 NTFMLYSGIKHECT-UHFFFAOYSA-N 0.000 description 1
- KXCQDIWJQBSUJF-UHFFFAOYSA-N 4-phenyl-1,3-thiazole Chemical compound S1C=NC(C=2C=CC=CC=2)=C1 KXCQDIWJQBSUJF-UHFFFAOYSA-N 0.000 description 1
- GPGKNEKFDGOXPO-UHFFFAOYSA-N 4-phenyl-1h-pyrazole Chemical compound C1=NNC=C1C1=CC=CC=C1 GPGKNEKFDGOXPO-UHFFFAOYSA-N 0.000 description 1
- FHUBTSLLILWICW-UHFFFAOYSA-N 4-phenyl-1h-quinazolin-2-one Chemical compound C12=CC=CC=C2NC(=O)N=C1C1=CC=CC=C1 FHUBTSLLILWICW-UHFFFAOYSA-N 0.000 description 1
- QLVZBXFOEUEIOZ-UHFFFAOYSA-N 4-phenyliminonaphthalen-1-one Chemical compound C12=CC=CC=C2C(=O)C=CC1=NC1=CC=CC=C1 QLVZBXFOEUEIOZ-UHFFFAOYSA-N 0.000 description 1
- MVTFMJPVPXNIFC-UHFFFAOYSA-N 4-phenylisoquinoline Chemical compound C1=CC=CC=C1C1=CN=CC2=CC=CC=C12 MVTFMJPVPXNIFC-UHFFFAOYSA-N 0.000 description 1
- LOCUXGFHUYBUHF-UHFFFAOYSA-N 4-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=NC2=CC=CC=C12 LOCUXGFHUYBUHF-UHFFFAOYSA-N 0.000 description 1
- KYDWNVBQXHQXPT-UHFFFAOYSA-N 4-sulfanylnaphthalen-1-ol Chemical compound C1=CC=C2C(O)=CC=C(S)C2=C1 KYDWNVBQXHQXPT-UHFFFAOYSA-N 0.000 description 1
- IVURTNNWJAPOML-UHFFFAOYSA-N 5,10-dihydrophenazine Chemical compound C1=CC=C2NC3=CC=CC=C3NC2=C1 IVURTNNWJAPOML-UHFFFAOYSA-N 0.000 description 1
- NYNSNUNMTUNAEO-UHFFFAOYSA-N 5,6,7,8-tetrahydronaphthalene-2-carbaldehyde Chemical compound C1CCCC2=CC(C=O)=CC=C21 NYNSNUNMTUNAEO-UHFFFAOYSA-N 0.000 description 1
- YPDRKSCNHYYJCO-UHFFFAOYSA-N 5,6-diphenyl-1,2,4-triazine Chemical compound C1=CC=CC=C1C1=NC=NN=C1C1=CC=CC=C1 YPDRKSCNHYYJCO-UHFFFAOYSA-N 0.000 description 1
- KLNUDQHISIUUAS-UHFFFAOYSA-N 5,7-dibromo-2-phenyl-1h-indole Chemical compound C=1C2=CC(Br)=CC(Br)=C2NC=1C1=CC=CC=C1 KLNUDQHISIUUAS-UHFFFAOYSA-N 0.000 description 1
- WMIDZSJJZVLDQI-UHFFFAOYSA-N 5,7-dichloro-2-phenyl-1h-indole Chemical compound C=1C2=CC(Cl)=CC(Cl)=C2NC=1C1=CC=CC=C1 WMIDZSJJZVLDQI-UHFFFAOYSA-N 0.000 description 1
- FYZHLRMYDRUDES-UHFFFAOYSA-N 5,7-dimethylocta-1,6-diene Chemical compound CC(C)=CC(C)CCC=C FYZHLRMYDRUDES-UHFFFAOYSA-N 0.000 description 1
- ZFPXYLWYSNUYNG-UHFFFAOYSA-N 5-(4-aminophenyl)-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound C1=CC(N)=CC=C1C1=NC(=S)NN1 ZFPXYLWYSNUYNG-UHFFFAOYSA-N 0.000 description 1
- YBKRZMVRSWNPRC-UHFFFAOYSA-N 5-(4-fluorophenyl)-1,3-thiazole Chemical compound C1=CC(F)=CC=C1C1=CN=CS1 YBKRZMVRSWNPRC-UHFFFAOYSA-N 0.000 description 1
- NGNNFDYHJKDHJN-UHFFFAOYSA-N 5-aminoimidazole-2,4-dione Chemical compound N=C1NC(=O)NC1=O NGNNFDYHJKDHJN-UHFFFAOYSA-N 0.000 description 1
- CYJZJGYYTFQQBY-UHFFFAOYSA-N 5-bromoisoquinoline Chemical compound N1=CC=C2C(Br)=CC=CC2=C1 CYJZJGYYTFQQBY-UHFFFAOYSA-N 0.000 description 1
- VVIOWSQDCCLDJX-UHFFFAOYSA-N 5-chloro-1,2-diphenylimidazole Chemical compound C=1C=CC=CC=1N1C(Cl)=CN=C1C1=CC=CC=C1 VVIOWSQDCCLDJX-UHFFFAOYSA-N 0.000 description 1
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 1
- WMFXCDGQRHJFKL-UHFFFAOYSA-N 5-fluoroquinoline Chemical compound C1=CC=C2C(F)=CC=CC2=N1 WMFXCDGQRHJFKL-UHFFFAOYSA-N 0.000 description 1
- CUILFTFMBBGSFT-UHFFFAOYSA-N 5-iodoisoquinoline Chemical compound N1=CC=C2C(I)=CC=CC2=C1 CUILFTFMBBGSFT-UHFFFAOYSA-N 0.000 description 1
- MULZWPFQTUDZPD-UHFFFAOYSA-N 5-methyl-2-phenyl-1,3-oxazole Chemical compound O1C(C)=CN=C1C1=CC=CC=C1 MULZWPFQTUDZPD-UHFFFAOYSA-N 0.000 description 1
- TYOXIFXYEIILLY-UHFFFAOYSA-N 5-methyl-2-phenyl-1h-imidazole Chemical compound N1C(C)=CN=C1C1=CC=CC=C1 TYOXIFXYEIILLY-UHFFFAOYSA-N 0.000 description 1
- QHRSESMSOJZMCO-UHFFFAOYSA-N 5-methyl-3-phenyl-1h-pyrazole Chemical compound N1C(C)=CC(C=2C=CC=CC=2)=N1 QHRSESMSOJZMCO-UHFFFAOYSA-N 0.000 description 1
- JJQPALVTXOQWGU-UHFFFAOYSA-N 5-methyl-4-phenyl-1,3-thiazole Chemical compound S1C=NC(C=2C=CC=CC=2)=C1C JJQPALVTXOQWGU-UHFFFAOYSA-N 0.000 description 1
- PYGMPFQCCWBTJQ-UHFFFAOYSA-N 5-nitroisoquinoline Chemical compound N1=CC=C2C([N+](=O)[O-])=CC=CC2=C1 PYGMPFQCCWBTJQ-UHFFFAOYSA-N 0.000 description 1
- YPYPBEGIASEWKA-UHFFFAOYSA-N 5-phenyl-1,3-oxazole Chemical compound O1C=NC=C1C1=CC=CC=C1 YPYPBEGIASEWKA-UHFFFAOYSA-N 0.000 description 1
- XHLKOHSAWQPOFO-UHFFFAOYSA-N 5-phenyl-1h-imidazole Chemical compound N1C=NC=C1C1=CC=CC=C1 XHLKOHSAWQPOFO-UHFFFAOYSA-N 0.000 description 1
- AWLDDDPIAFHCFV-UHFFFAOYSA-N 5-phenyl-1h-pyrrole-2-carbaldehyde Chemical compound N1C(C=O)=CC=C1C1=CC=CC=C1 AWLDDDPIAFHCFV-UHFFFAOYSA-N 0.000 description 1
- MARUHZGHZWCEQU-UHFFFAOYSA-N 5-phenyl-2h-tetrazole Chemical compound C1=CC=CC=C1C1=NNN=N1 MARUHZGHZWCEQU-UHFFFAOYSA-N 0.000 description 1
- NYJHOCZVKHRRLG-UHFFFAOYSA-N 5-phenyldithiole-3-thione Chemical group S1SC(=S)C=C1C1=CC=CC=C1 NYJHOCZVKHRRLG-UHFFFAOYSA-N 0.000 description 1
- NWOANCZCVIUCTG-UHFFFAOYSA-N 5-phenyltetrazol-1-amine Chemical compound NN1N=NN=C1C1=CC=CC=C1 NWOANCZCVIUCTG-UHFFFAOYSA-N 0.000 description 1
- MXTVVTVVBOYKCU-UHFFFAOYSA-N 5-phenylthiadiazole Chemical compound N1=NSC(C=2C=CC=CC=2)=C1 MXTVVTVVBOYKCU-UHFFFAOYSA-N 0.000 description 1
- XHVULKQHRQZNMW-UHFFFAOYSA-N 5H-benzocycloheptene Chemical compound C1C=CC=CC2=CC=CC=C12 XHVULKQHRQZNMW-UHFFFAOYSA-N 0.000 description 1
- QGXBDMJGAMFCBF-HLUDHZFRSA-N 5α-Androsterone Chemical compound C1[C@H](O)CC[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CC[C@H]21 QGXBDMJGAMFCBF-HLUDHZFRSA-N 0.000 description 1
- POAVRNPUPPJLKZ-UHFFFAOYSA-N 6,11-dihydro-5h-dibenzo[1,2-a:1',2'-e][7]annulen-11-ol Chemical compound C1CC2=CC=CC=C2C(O)C2=CC=CC=C21 POAVRNPUPPJLKZ-UHFFFAOYSA-N 0.000 description 1
- KNSJCCNMJYXLOL-UHFFFAOYSA-N 6,12-epoxy-6h,12h-dibenzo[b,f][1,5]dioxocin Chemical compound O1C2=CC=CC=C2C2OC1C1=CC=CC=C1O2 KNSJCCNMJYXLOL-UHFFFAOYSA-N 0.000 description 1
- SNZIMMWYSCVVFG-UHFFFAOYSA-N 6,13-dihydropentacene Chemical compound C1=CC=C2C=C3CC4=CC5=CC=CC=C5C=C4CC3=CC2=C1 SNZIMMWYSCVVFG-UHFFFAOYSA-N 0.000 description 1
- JKOCGAMDKVAHCI-UHFFFAOYSA-N 6,7-Benzocoumarin Chemical compound C1=CC=C2C=C(OC(=O)C=C3)C3=CC2=C1 JKOCGAMDKVAHCI-UHFFFAOYSA-N 0.000 description 1
- WMAPLTCNVJVJNP-UHFFFAOYSA-N 6,7-dimethoxy-2-phenyl-1-benzofuran Chemical compound COC1=C(C2=C(C=C(O2)C2=CC=CC=C2)C=C1)OC WMAPLTCNVJVJNP-UHFFFAOYSA-N 0.000 description 1
- CQBUOADZONQUQT-UHFFFAOYSA-N 6-benzoylcyclohexa-2,4-dien-1-one Chemical compound C=1C=CC=CC=1C(=O)C1C=CC=CC1=O CQBUOADZONQUQT-UHFFFAOYSA-N 0.000 description 1
- VDOYSQQOKJDYDR-UHFFFAOYSA-N 6-ethylquinoline Chemical compound N1=CC=CC2=CC(CC)=CC=C21 VDOYSQQOKJDYDR-UHFFFAOYSA-N 0.000 description 1
- RMDCSDVIVXJELQ-UHFFFAOYSA-N 6-fluoroquinoline Chemical compound N1=CC=CC2=CC(F)=CC=C21 RMDCSDVIVXJELQ-UHFFFAOYSA-N 0.000 description 1
- GJEZBVHHZQAEDB-UHFFFAOYSA-N 6-oxabicyclo[3.1.0]hexane Chemical compound C1CCC2OC21 GJEZBVHHZQAEDB-UHFFFAOYSA-N 0.000 description 1
- DTKWJHIAZGYBLD-UHFFFAOYSA-N 6-phenylchromen-2-one Chemical compound C=1C=C2OC(=O)C=CC2=CC=1C1=CC=CC=C1 DTKWJHIAZGYBLD-UHFFFAOYSA-N 0.000 description 1
- XXWONCALJGBUFK-UHFFFAOYSA-N 6-phenylphenanthridine Chemical class C1=CC=CC=C1C1=NC2=CC=CC=C2C2=CC=CC=C12 XXWONCALJGBUFK-UHFFFAOYSA-N 0.000 description 1
- OKLKICXAGRLLGF-UHFFFAOYSA-N 6-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=C(N=CC=C2)C2=C1 OKLKICXAGRLLGF-UHFFFAOYSA-N 0.000 description 1
- DTGNUIQZXLZDTM-UHFFFAOYSA-N 7-bromo-5-chloro-2-phenyl-1h-indole Chemical compound C=1C2=CC(Cl)=CC(Br)=C2NC=1C1=CC=CC=C1 DTGNUIQZXLZDTM-UHFFFAOYSA-N 0.000 description 1
- KJCITCNQWWFFQM-UHFFFAOYSA-N 7-chloro-2-phenyl-1h-indole Chemical compound N1C=2C(Cl)=CC=CC=2C=C1C1=CC=CC=C1 KJCITCNQWWFFQM-UHFFFAOYSA-N 0.000 description 1
- JYRVSRMFQWYDGM-UHFFFAOYSA-N 7-cyclopenta-2,4-dien-1-ylidenecyclohepta-1,3,5-triene Chemical compound C1=CC=CC1=C1C=CC=CC=C1 JYRVSRMFQWYDGM-UHFFFAOYSA-N 0.000 description 1
- XUIRHRWOJCYEDJ-UHFFFAOYSA-N 7-fluoroquinoline Chemical compound C1=CC=NC2=CC(F)=CC=C21 XUIRHRWOJCYEDJ-UHFFFAOYSA-N 0.000 description 1
- OOYSHAXCXQSKEM-UHFFFAOYSA-N 7-methyl-2-(4-methylphenyl)-1H-1,2,3,4-benzotetrazine Chemical compound Cc1ccc(cc1)N1Nc2cc(C)ccc2N=N1 OOYSHAXCXQSKEM-UHFFFAOYSA-N 0.000 description 1
- YPWFNLSXQIGJCK-UHFFFAOYSA-N 7-oxabicyclo[2.2.1]heptane Chemical compound C1CC2CCC1O2 YPWFNLSXQIGJCK-UHFFFAOYSA-N 0.000 description 1
- ODPYDILFQYARBK-UHFFFAOYSA-N 7-thiabicyclo[4.1.0]hepta-1,3,5-triene Chemical compound C1=CC=C2SC2=C1 ODPYDILFQYARBK-UHFFFAOYSA-N 0.000 description 1
- AATMCCVYMZDTCD-UHFFFAOYSA-N 7H-benzocycloheptene Chemical compound C1=CCC=CC2=CC=CC=C21 AATMCCVYMZDTCD-UHFFFAOYSA-N 0.000 description 1
- WREVVZMUNPAPOV-UHFFFAOYSA-N 8-aminoquinoline Chemical compound C1=CN=C2C(N)=CC=CC2=C1 WREVVZMUNPAPOV-UHFFFAOYSA-N 0.000 description 1
- RNAAXKYOTPSFGV-UHFFFAOYSA-N 8-fluoroquinoline Chemical compound C1=CN=C2C(F)=CC=CC2=C1 RNAAXKYOTPSFGV-UHFFFAOYSA-N 0.000 description 1
- JZENKAZHWWTAGL-UHFFFAOYSA-N 8-methyl-1,7-phenanthroline Chemical compound C1=CN=C2C3=CC=C(C)N=C3C=CC2=C1 JZENKAZHWWTAGL-UHFFFAOYSA-N 0.000 description 1
- PCFMUWBCZZUMRX-UHFFFAOYSA-N 9,10-Dihydroxyanthracene Chemical compound C1=CC=C2C(O)=C(C=CC=C3)C3=C(O)C2=C1 PCFMUWBCZZUMRX-UHFFFAOYSA-N 0.000 description 1
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 1
- 229940076442 9,10-anthraquinone Drugs 0.000 description 1
- JURXVMQHSBALPL-UHFFFAOYSA-N 9,10-diethylphenanthrene Chemical compound C1=CC=C2C(CC)=C(CC)C3=CC=CC=C3C2=C1 JURXVMQHSBALPL-UHFFFAOYSA-N 0.000 description 1
- XYPMAZCBFKBIFK-UHFFFAOYSA-N 9,10-dinitroanthracene Chemical compound C1=CC=C2C([N+](=O)[O-])=C(C=CC=C3)C3=C([N+]([O-])=O)C2=C1 XYPMAZCBFKBIFK-UHFFFAOYSA-N 0.000 description 1
- SECWSIFCFMVOAN-UHFFFAOYSA-N 9,10-diphenylphenanthrene Chemical compound C1=CC=CC=C1C(C1=CC=CC=C1C1=CC=CC=C11)=C1C1=CC=CC=C1 SECWSIFCFMVOAN-UHFFFAOYSA-N 0.000 description 1
- YYVYAPXYZVYDHN-UHFFFAOYSA-N 9,10-phenanthroquinone Chemical compound C1=CC=C2C(=O)C(=O)C3=CC=CC=C3C2=C1 YYVYAPXYZVYDHN-UHFFFAOYSA-N 0.000 description 1
- GPYAGEJQCXTMET-UHFFFAOYSA-N 9,9-diphenylxanthene Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C1(C=1C=CC=CC=1)C1=CC=CC=C1 GPYAGEJQCXTMET-UHFFFAOYSA-N 0.000 description 1
- XHJCHUVWJCDJPN-UHFFFAOYSA-N 9-bromo-10-nitrophenanthrene Chemical compound C1=CC=C2C([N+](=O)[O-])=C(Br)C3=CC=CC=C3C2=C1 XHJCHUVWJCDJPN-UHFFFAOYSA-N 0.000 description 1
- OGOYZCQQQFAGRI-UHFFFAOYSA-N 9-ethenylanthracene Chemical compound C1=CC=C2C(C=C)=C(C=CC=C3)C3=CC2=C1 OGOYZCQQQFAGRI-UHFFFAOYSA-N 0.000 description 1
- YBIPHTBHFGUBBX-UHFFFAOYSA-N 9-nitrophenanthren-3-ol Chemical compound C1=CC=C2C3=CC(O)=CC=C3C=C([N+]([O-])=O)C2=C1 YBIPHTBHFGUBBX-UHFFFAOYSA-N 0.000 description 1
- MFCLDPQGJMEEBE-UHFFFAOYSA-N 9-phenoxyacridine Chemical compound C=12C=CC=CC2=NC2=CC=CC=C2C=1OC1=CC=CC=C1 MFCLDPQGJMEEBE-UHFFFAOYSA-N 0.000 description 1
- VLEHHVSMUYZMDB-UHFFFAOYSA-N 9-phenyl-11h-benzo[a]fluorene Chemical compound C=1C=C2C3=CC=C4C=CC=CC4=C3CC2=CC=1C1=CC=CC=C1 VLEHHVSMUYZMDB-UHFFFAOYSA-N 0.000 description 1
- JAPCXGFREZPNHK-UHFFFAOYSA-N 9-phenyl-9h-xanthene Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C1C1=CC=CC=C1 JAPCXGFREZPNHK-UHFFFAOYSA-N 0.000 description 1
- MTRFEWTWIPAXLG-UHFFFAOYSA-N 9-phenylacridine Chemical compound C1=CC=CC=C1C1=C(C=CC=C2)C2=NC2=CC=CC=C12 MTRFEWTWIPAXLG-UHFFFAOYSA-N 0.000 description 1
- OEHBIJLLEOFRNN-UHFFFAOYSA-N 9-pyridin-3-ylacridine Chemical compound C=12C=CC=CC2=NC2=CC=CC=C2C=1C1=CC=CN=C1 OEHBIJLLEOFRNN-UHFFFAOYSA-N 0.000 description 1
- SXXWAWNPJCEOGD-UHFFFAOYSA-N 9-xanthen-9-ylidenexanthene Chemical group C12=CC=CC=C2OC2=CC=CC=C2C1=C1C2=CC=CC=C2OC2=CC=CC=C21 SXXWAWNPJCEOGD-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 229930008281 A03AD01 - Papaverine Natural products 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- MUJFBNIGLPDCAE-UHFFFAOYSA-N Acronidine Natural products C1=CC(C)(C)OC2=C1C1=C(OC)C(C=CO3)=C3N=C1C=C2OC MUJFBNIGLPDCAE-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- DVICWXUADSCSLL-DDEWRDOISA-N Alloxanthin/Tetradehydrozeaxanthin/(Cynthiaxanthin)/(Pectenoxanthin) Chemical compound C([C@H](O)CC=1C)C(C)(C)C=1C#CC(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)C#CC1=C(C)C[C@@H](O)CC1(C)C DVICWXUADSCSLL-DDEWRDOISA-N 0.000 description 1
- 229920000945 Amylopectin Polymers 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- TXVHTIQJNYSSKO-UHFFFAOYSA-N BeP Natural products C1=CC=C2C3=CC=CC=C3C3=CC=CC4=CC=C1C2=C34 TXVHTIQJNYSSKO-UHFFFAOYSA-N 0.000 description 1
- KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- DBMJZOMNXBSRED-UHFFFAOYSA-N Bergamottin Natural products O1C(=O)C=CC2=C1C=C1OC=CC1=C2OCC=C(C)CCC=C(C)C DBMJZOMNXBSRED-UHFFFAOYSA-N 0.000 description 1
- GWZYPXHJIZCRAJ-UHFFFAOYSA-N Biliverdin Natural products CC1=C(C=C)C(=C/C2=NC(=Cc3[nH]c(C=C/4NC(=O)C(=C4C)C=C)c(C)c3CCC(=O)O)C(=C2C)CCC(=O)O)NC1=O GWZYPXHJIZCRAJ-UHFFFAOYSA-N 0.000 description 1
- RCNSAJSGRJSBKK-NSQVQWHSSA-N Biliverdin IX Chemical compound N1C(=O)C(C)=C(C=C)\C1=C\C1=C(C)C(CCC(O)=O)=C(\C=C/2C(=C(C)C(=C/C=3C(=C(C=C)C(=O)N=3)C)/N\2)CCC(O)=O)N1 RCNSAJSGRJSBKK-NSQVQWHSSA-N 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- LURGALYXLLHNTD-UHFFFAOYSA-N BrC(C1=C2)=CC3=CC=CC=C3C1=N[S+]2C1=CC=CC=C1 Chemical compound BrC(C1=C2)=CC3=CC=CC=C3C1=N[S+]2C1=CC=CC=C1 LURGALYXLLHNTD-UHFFFAOYSA-N 0.000 description 1
- LMLAXZNAJDHGRI-UHFFFAOYSA-M Br[Mg]c1c2ccccc2c(Br)c2ccccc12 Chemical compound Br[Mg]c1c2ccccc2c(Br)c2ccccc12 LMLAXZNAJDHGRI-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- MRABAEUHTLLEML-UHFFFAOYSA-N Butyl lactate Chemical compound CCCCOC(=O)C(C)O MRABAEUHTLLEML-UHFFFAOYSA-N 0.000 description 1
- SQIGIJKLVVZGBR-UHFFFAOYSA-N C1(=CC=CC2=CC=CC=C12)C(=O)C1=CC=CC2=CC=CC=C12.C1(=CC=CC=C1)C1=CC=CC=C1 Chemical compound C1(=CC=CC2=CC=CC=C12)C(=O)C1=CC=CC2=CC=CC=C12.C1(=CC=CC=C1)C1=CC=CC=C1 SQIGIJKLVVZGBR-UHFFFAOYSA-N 0.000 description 1
- RAWNHOPITXYBPP-UHFFFAOYSA-N C1(=CC=CC=C1)C(O)(C1OC=CC=C1)C1=CC=CC=C1 Chemical compound C1(=CC=CC=C1)C(O)(C1OC=CC=C1)C1=CC=CC=C1 RAWNHOPITXYBPP-UHFFFAOYSA-N 0.000 description 1
- PHQMNHHPDQEUBE-UHFFFAOYSA-N C1=CC=CC=2C3=CC=CC=C3C=CC12.O1OC=CC=C1 Chemical compound C1=CC=CC=2C3=CC=CC=C3C=CC12.O1OC=CC=C1 PHQMNHHPDQEUBE-UHFFFAOYSA-N 0.000 description 1
- ZTEDPPUXWFWGFL-UHFFFAOYSA-N C=CC(OC1=CC(C#N)=CSC1)=O Chemical compound C=CC(OC1=CC(C#N)=CSC1)=O ZTEDPPUXWFWGFL-UHFFFAOYSA-N 0.000 description 1
- MBUABWWWKZZYEH-UHFFFAOYSA-N C=CC.C1=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45 Chemical group C=CC.C1=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45 MBUABWWWKZZYEH-UHFFFAOYSA-N 0.000 description 1
- ROQHAEDYUXKRRV-UHFFFAOYSA-N CC(C=C)N=C=N Chemical compound CC(C=C)N=C=N ROQHAEDYUXKRRV-UHFFFAOYSA-N 0.000 description 1
- PKYRDBZZQORFMX-UHFFFAOYSA-N CC1=C2C(=C(C(C(=C3C(=C(C(=C(C=4C(=NC(=NC5=NN=C1N5)N4)C)C)N3)C)C)C)=N2)C)C.[Mg] Chemical compound CC1=C2C(=C(C(C(=C3C(=C(C(=C(C=4C(=NC(=NC5=NN=C1N5)N4)C)C)N3)C)C)C)=N2)C)C.[Mg] PKYRDBZZQORFMX-UHFFFAOYSA-N 0.000 description 1
- SCQWVVLHQGLIJS-UHFFFAOYSA-N CC1=CC=CC2=CC(C)=CC=C21.C1=CC=C(C)C2=CC(C)=CC=C21 Chemical compound CC1=CC=CC2=CC(C)=CC=C21.C1=CC=C(C)C2=CC(C)=CC=C21 SCQWVVLHQGLIJS-UHFFFAOYSA-N 0.000 description 1
- CBWYGECGCQPVBS-UHFFFAOYSA-N CCN1C(C2=CC=CC=C2)=NC(Cl)=C1 Chemical compound CCN1C(C2=CC=CC=C2)=NC(Cl)=C1 CBWYGECGCQPVBS-UHFFFAOYSA-N 0.000 description 1
- AJHQZABDXFJKHY-UHFFFAOYSA-N C[S+]1N=C(C=CC2=CC=CC=C22)C2=C1 Chemical compound C[S+]1N=C(C=CC2=CC=CC=C22)C2=C1 AJHQZABDXFJKHY-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 240000006162 Chenopodium quinoa Species 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- DQRWOEOJTKIGGI-UHFFFAOYSA-N ClC1=C(C=CC(=C1)Cl)N1NC(=C(NN1C1=C(C=C(C=C1)Cl)Cl)C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound ClC1=C(C=CC(=C1)Cl)N1NC(=C(NN1C1=C(C=C(C=C1)Cl)Cl)C1=CC=CC=C1)C1=CC=CC=C1 DQRWOEOJTKIGGI-UHFFFAOYSA-N 0.000 description 1
- OKORHWXYDBSYNO-UHFFFAOYSA-N Codamine Natural products C1=C(OC)C(OC)=CC=C1CC1C2=CC(O)=C(OC)C=C2CCN1C OKORHWXYDBSYNO-UHFFFAOYSA-N 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- RIXOVHWIYRZQDC-UHFFFAOYSA-N Cusparine Natural products C1=CC=C2C(OC)=CC(CCC=3C=C4OCOC4=CC=3)=NC2=C1 RIXOVHWIYRZQDC-UHFFFAOYSA-N 0.000 description 1
- HBQJTBXZMPSVBP-UHFFFAOYSA-N Cyanidine Natural products OC1=CC(=C2/Oc3cc(O)cc(O)c3C=C2O)C=CC1=O HBQJTBXZMPSVBP-UHFFFAOYSA-N 0.000 description 1
- YIQVPNZGGSTDKI-UHFFFAOYSA-N D-bicucculine Natural products C12=CC=C3OCOC3=C2C(=O)OC1C1C2=CC(OCO3)=C3C=C2CCN1 YIQVPNZGGSTDKI-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- FWKBXSPDFCAHFN-UHFFFAOYSA-N Dracorubin Natural products C1CC=2C(OC)=CC=3OC(C=45)=C(C)C(=O)C=C5OC(C=5C=CC=CC=5)=CC=4C=3C=2OC1C1=CC=CC=C1 FWKBXSPDFCAHFN-UHFFFAOYSA-N 0.000 description 1
- 102100025027 E3 ubiquitin-protein ligase TRIM69 Human genes 0.000 description 1
- 241000257465 Echinoidea Species 0.000 description 1
- DNXHEGUUPJUMQT-CBZIJGRNSA-N Estrone Chemical compound OC1=CC=C2[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 DNXHEGUUPJUMQT-CBZIJGRNSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- XXRCUYVCPSWGCC-UHFFFAOYSA-N Ethyl pyruvate Chemical compound CCOC(=O)C(C)=O XXRCUYVCPSWGCC-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- QGXBDMJGAMFCBF-UHFFFAOYSA-N Etiocholanolone Natural products C1C(O)CCC2(C)C3CCC(C)(C(CC4)=O)C4C3CCC21 QGXBDMJGAMFCBF-UHFFFAOYSA-N 0.000 description 1
- OPUFDNZTKHPZHM-UHFFFAOYSA-N Euparin Chemical compound CC(=O)C1=C(O)C=C2OC(C(=C)C)=CC2=C1 OPUFDNZTKHPZHM-UHFFFAOYSA-N 0.000 description 1
- FDFXOWJHWJKKRT-UHFFFAOYSA-N Evolatine Natural products N1=C2C=C(OCC(O)C(C)(C)O)C(OC)=CC2=C(OC)C2=C1OC=C2 FDFXOWJHWJKKRT-UHFFFAOYSA-N 0.000 description 1
- OIYFAUVFZZOOFG-INIZCTEOSA-N Evoxine Natural products COc1c(OC[C@H](O)C(C)(C)O)ccc2c(OC)c3ccoc3cc12 OIYFAUVFZZOOFG-INIZCTEOSA-N 0.000 description 1
- QJWPOMFSLSFMET-UHFFFAOYSA-N Evoxoidine Natural products N1=C2C(OC)=C(OCC(=O)C(C)C)C=CC2=C(OC)C2=C1OC=C2 QJWPOMFSLSFMET-UHFFFAOYSA-N 0.000 description 1
- IMDNUXFWNXWHQT-UHFFFAOYSA-N Flindersine Natural products CC1(C)OC2C(C=C1)C(=O)Nc3ccccc23 IMDNUXFWNXWHQT-UHFFFAOYSA-N 0.000 description 1
- IMIXFUXOSFSXPC-IYIVSNSKSA-N Fukugetin Chemical compound C1=CC(O)=CC=C1[C@H]1[C@H](C=2C=3OC(CC(=O)C=3C(O)=CC=2O)C=2C=C(O)C(O)=CC=2)C(=O)C2=C(O)C=C(O)C=C2O1 IMIXFUXOSFSXPC-IYIVSNSKSA-N 0.000 description 1
- GFWPWSNIXRDQJC-LMSSTIIKSA-N Fukugetin Natural products C1=CC(O)=CC=C1[C@@H]1[C@@H](C=2C3=C(C(C=C(O3)C=3C=C(O)C(O)=CC=3)=O)C(O)=CC=2O)C(=O)C2=C(O)C=C(O)C=C2O1 GFWPWSNIXRDQJC-LMSSTIIKSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- 229920002527 Glycogen Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000000899 Gutta-Percha Substances 0.000 description 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 101000830203 Homo sapiens E3 ubiquitin-protein ligase TRIM69 Proteins 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- SDPOFOYJCOPMMV-UHFFFAOYSA-N Kokusagine Natural products C1=C2C(OC)=C(C=CO3)C3=NC2=C2OCOC2=C1 SDPOFOYJCOPMMV-UHFFFAOYSA-N 0.000 description 1
- LYBYYVXQSFDBQO-INIZCTEOSA-N L-(+)-Laudanidine Natural products O(C)c1c(OC)cc2c([C@H](Cc3cc(O)c(OC)cc3)[N+](C)CC2)c1 LYBYYVXQSFDBQO-INIZCTEOSA-N 0.000 description 1
- KGPAYJZAMGEDIQ-KRWDZBQOSA-N Laudanosine Chemical compound C1=C(OC)C(OC)=CC=C1C[C@H]1C2=CC(OC)=C(OC)C=C2CCN1C KGPAYJZAMGEDIQ-KRWDZBQOSA-N 0.000 description 1
- VHRSWCTVFBWHKE-UHFFFAOYSA-N Laudanosoline Chemical compound CN1CCC2=CC(O)=C(O)C=C2C1CC1=CC=C(O)C(O)=C1 VHRSWCTVFBWHKE-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- WVBLHNOAFTUBSS-UHFFFAOYSA-N Medicosmine Natural products O1C(C)(C)C=CC2=C3C(OC)=C(C=CO4)C4=NC3=CC=C21 WVBLHNOAFTUBSS-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- PEWWLIQAXYMMAN-UHFFFAOYSA-N Melicopine Chemical compound C1=CC=C2C(=O)C3=C(OC)C(OC)=C(OCO4)C4=C3N(C)C2=C1 PEWWLIQAXYMMAN-UHFFFAOYSA-N 0.000 description 1
- NKZNKBLXNLBATF-UHFFFAOYSA-N Melicopine Natural products CN1C2=CC=CC=C2C(=O)C(C=C2OC)=C1C1=C2OCO1 NKZNKBLXNLBATF-UHFFFAOYSA-N 0.000 description 1
- ABSPRNADVQNDOU-UHFFFAOYSA-N Menaquinone 1 Natural products C1=CC=C2C(=O)C(CC=C(C)C)=C(C)C(=O)C2=C1 ABSPRNADVQNDOU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- RJTOSFZZYBCYTM-UHFFFAOYSA-N Moperone hydrochloride Chemical compound [Cl-].C1=CC(C)=CC=C1C1(O)CC[NH+](CCCC(=O)C=2C=CC(F)=CC=2)CC1 RJTOSFZZYBCYTM-UHFFFAOYSA-N 0.000 description 1
- NNOTUGMONRPGDJ-UHFFFAOYSA-N N(=O)C=1C(=NOC1)C1=CC=CC=C1 Chemical compound N(=O)C=1C(=NOC1)C1=CC=CC=C1 NNOTUGMONRPGDJ-UHFFFAOYSA-N 0.000 description 1
- UTGQNNCQYDRXCH-UHFFFAOYSA-N N,N'-diphenyl-1,4-phenylenediamine Chemical compound C=1C=C(NC=2C=CC=CC=2)C=CC=1NC1=CC=CC=C1 UTGQNNCQYDRXCH-UHFFFAOYSA-N 0.000 description 1
- NULAJYZBOLVQPQ-UHFFFAOYSA-N N-(1-naphthyl)ethylenediamine Chemical compound C1=CC=C2C(NCCN)=CC=CC2=C1 NULAJYZBOLVQPQ-UHFFFAOYSA-N 0.000 description 1
- CWFINLADSFPMHF-UHFFFAOYSA-N N-hydroxynaphthalen-1-amine Chemical compound C1=CC=C2C(NO)=CC=CC2=C1 CWFINLADSFPMHF-UHFFFAOYSA-N 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 101100103030 Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) xanC gene Proteins 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CAOJVPRATKOZIN-UHFFFAOYSA-N O=C1CC(=CC=C1)C(C1=CC=CC=C1)=O Chemical compound O=C1CC(=CC=C1)C(C1=CC=CC=C1)=O CAOJVPRATKOZIN-UHFFFAOYSA-N 0.000 description 1
- LCTBJGTVIYGQMA-UHFFFAOYSA-N O=C=CCSCC=C=O Chemical compound O=C=CCSCC=C=O LCTBJGTVIYGQMA-UHFFFAOYSA-N 0.000 description 1
- FQCPXIJRWHRHIP-UHFFFAOYSA-N Oroselone Natural products C1=CC(=O)OC2=C1C=CC1=C2C=C(C(=C)C)O1 FQCPXIJRWHRHIP-UHFFFAOYSA-N 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- 240000000342 Palaquium gutta Species 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- XPFRXWCVYUEORT-UHFFFAOYSA-N Phenacemide Chemical compound NC(=O)NC(=O)CC1=CC=CC=C1 XPFRXWCVYUEORT-UHFFFAOYSA-N 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- HCOLPNRPCMFHOH-UHFFFAOYSA-N Prodigiosin Natural products CCCCCC1C=C(C=C/2N=C(C=C2OC)c3ccc[nH]3)N=C1C HCOLPNRPCMFHOH-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 108091034057 RNA (poly(A)) Proteins 0.000 description 1
- PLXBWHJQWKZRKG-UHFFFAOYSA-N Resazurin Chemical compound C1=CC(=O)C=C2OC3=CC(O)=CC=C3[N+]([O-])=C21 PLXBWHJQWKZRKG-UHFFFAOYSA-N 0.000 description 1
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 108010013296 Sericins Proteins 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- TYOWQSLRVAUSMI-UHFFFAOYSA-N Sterecobilin-IXalpha Natural products N1C(=O)C(C)C(CC)C1CC(C(=C1CCC(O)=O)C)=NC1=CC1=C(CCC(O)=O)C(C)=C(CC2C(C(CC)C(=O)N2)C)N1 TYOWQSLRVAUSMI-UHFFFAOYSA-N 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- MRQIXHXHHPWVIL-ISLYRVAYSA-N Sudan I Chemical compound OC1=CC=C2C=CC=CC2=C1\N=N\C1=CC=CC=C1 MRQIXHXHHPWVIL-ISLYRVAYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- PQECCKIOFCWGRJ-UHFFFAOYSA-N Tetrahydro-berberine Natural products C1=C2C3CC4=CC=C(OC)C(O)=C4CN3CCC2=CC2=C1OCO2 PQECCKIOFCWGRJ-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- FTIHFTVXYNBUSM-BUHFOSPRSA-N [(e)-1,2-dichloro-2-phenylethenyl]benzene Chemical compound C=1C=CC=CC=1C(/Cl)=C(\Cl)C1=CC=CC=C1 FTIHFTVXYNBUSM-BUHFOSPRSA-N 0.000 description 1
- OVZXISBUYCEVEV-OUKQBFOZSA-N [(e)-1-phenylprop-1-en-2-yl]benzene Chemical compound C=1C=CC=CC=1C(/C)=C/C1=CC=CC=C1 OVZXISBUYCEVEV-OUKQBFOZSA-N 0.000 description 1
- XDLYGHNFZIWNMG-ISLYRVAYSA-N [(e)-4-phenylhex-3-en-3-yl]benzene Chemical compound C=1C=CC=CC=1C(/CC)=C(\CC)C1=CC=CC=C1 XDLYGHNFZIWNMG-ISLYRVAYSA-N 0.000 description 1
- QIFBVYLHLLTNLI-KAMYIIQDSA-N [(z)-2-nitro-2-phenylethenyl]benzene Chemical compound C=1C=CC=CC=1/C([N+](=O)[O-])=C/C1=CC=CC=C1 QIFBVYLHLLTNLI-KAMYIIQDSA-N 0.000 description 1
- BQFJXYBNTQREBM-UHFFFAOYSA-N [1,3]thiazolo[4,5-h]quinoline Chemical compound C1=CC=NC2=C(SC=N3)C3=CC=C21 BQFJXYBNTQREBM-UHFFFAOYSA-N 0.000 description 1
- FJSWJJOLFPIDER-UHFFFAOYSA-N [3-(methanesulfonamidomethyl)phenyl]boronic acid Chemical compound CS(=O)(=O)NCC1=CC=CC(B(O)O)=C1 FJSWJJOLFPIDER-UHFFFAOYSA-N 0.000 description 1
- BRHJUILQKFBMTL-UHFFFAOYSA-N [4,4-bis(dimethylamino)cyclohexa-1,5-dien-1-yl]-phenylmethanone Chemical compound C1=CC(N(C)C)(N(C)C)CC=C1C(=O)C1=CC=CC=C1 BRHJUILQKFBMTL-UHFFFAOYSA-N 0.000 description 1
- KIPLYOUQVMMOHB-MXWBXKMOSA-L [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O Chemical compound [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O KIPLYOUQVMMOHB-MXWBXKMOSA-L 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- JYPJNTLDVNRJMG-UHFFFAOYSA-L [S-]SS[S-].[Na+].C(CCl)Cl.[Na+] Chemical compound [S-]SS[S-].[Na+].C(CCl)Cl.[Na+] JYPJNTLDVNRJMG-UHFFFAOYSA-L 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 1
- 125000004054 acenaphthylenyl group Chemical group C1(=CC2=CC=CC3=CC=CC1=C23)* 0.000 description 1
- NOSIYYJFMPDDSA-UHFFFAOYSA-N acepromazine Chemical compound C1=C(C(C)=O)C=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 NOSIYYJFMPDDSA-UHFFFAOYSA-N 0.000 description 1
- URSFLPCGEBSGAU-UHFFFAOYSA-N acetic acid anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C12.C(C)(=O)O.C(C)(=O)O URSFLPCGEBSGAU-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- KVXNKFYSHAUJIA-UHFFFAOYSA-N acetic acid;ethoxyethane Chemical compound CC(O)=O.CCOCC KVXNKFYSHAUJIA-UHFFFAOYSA-N 0.000 description 1
- ZUQXNLCTJRBSAC-UHFFFAOYSA-N acetic acid;naphthalen-1-ol Chemical compound CC(O)=O.C1=CC=C2C(O)=CC=CC2=C1 ZUQXNLCTJRBSAC-UHFFFAOYSA-N 0.000 description 1
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- BGLGAKMTYHWWKW-UHFFFAOYSA-N acridine yellow Chemical compound [H+].[Cl-].CC1=C(N)C=C2N=C(C=C(C(C)=C3)N)C3=CC2=C1 BGLGAKMTYHWWKW-UHFFFAOYSA-N 0.000 description 1
- FBSKJMQYURKNSU-ZLSOWSIRSA-N acteoside Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]1[C@H](OC(=O)\C=C\C=2C=C(O)C(O)=CC=2)[C@@H](CO)O[C@@H](OCCC=2C=C(O)C(O)=CC=2)[C@@H]1O FBSKJMQYURKNSU-ZLSOWSIRSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- DVICWXUADSCSLL-GUPSQEAKSA-N all-trans-Alloxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C#CC1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C#CC2=C(C)CC(O)CC2(C)C DVICWXUADSCSLL-GUPSQEAKSA-N 0.000 description 1
- UFRRRMXNFIGHPC-CPZJCIGYSA-N alloxanthin Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C#CC1=C(C)CC(O)CC1(C)C)C=CC=C(/C)C=CC#CC2=C(C)CC(O)CC2(C)C UFRRRMXNFIGHPC-CPZJCIGYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 1
- 150000005018 aminopurines Chemical class 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 229940061641 androsterone Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- YUENFNPLGJCNRB-UHFFFAOYSA-N anthracen-1-amine Chemical compound C1=CC=C2C=C3C(N)=CC=CC3=CC2=C1 YUENFNPLGJCNRB-UHFFFAOYSA-N 0.000 description 1
- KRLBTHCAZSDQCI-UHFFFAOYSA-N anthracene-1,10-dione Chemical compound C1=CC=C2C=C3C(=O)C=CC=C3C(=O)C2=C1 KRLBTHCAZSDQCI-UHFFFAOYSA-N 0.000 description 1
- RGHILYZRVFRRNK-UHFFFAOYSA-N anthracene-1,2-dione Chemical compound C1=CC=C2C=C(C(C(=O)C=C3)=O)C3=CC2=C1 RGHILYZRVFRRNK-UHFFFAOYSA-N 0.000 description 1
- LSOTZYUVGZKSHR-UHFFFAOYSA-N anthracene-1,4-dione Chemical compound C1=CC=C2C=C3C(=O)C=CC(=O)C3=CC2=C1 LSOTZYUVGZKSHR-UHFFFAOYSA-N 0.000 description 1
- PQJKLTRMSHJEEN-UHFFFAOYSA-N anthracene-1,5-dione Chemical compound O=C1C=CC=C2C=C3C(=O)C=CC=C3C=C21 PQJKLTRMSHJEEN-UHFFFAOYSA-N 0.000 description 1
- RSAFJKGIUBIAJP-UHFFFAOYSA-N anthracene-2,3-dione Chemical compound C1=CC=CC2=CC3=CC(=O)C(=O)C=C3C=C21 RSAFJKGIUBIAJP-UHFFFAOYSA-N 0.000 description 1
- SWYXZZAQKFGYFF-UHFFFAOYSA-N anthracene-2,6-dione Chemical compound O=C1C=CC2=CC3=CC(=O)C=CC3=CC2=C1 SWYXZZAQKFGYFF-UHFFFAOYSA-N 0.000 description 1
- YMNKUHIVVMFOFO-UHFFFAOYSA-N anthracene-9-carbaldehyde Chemical compound C1=CC=C2C(C=O)=C(C=CC=C3)C3=CC2=C1 YMNKUHIVVMFOFO-UHFFFAOYSA-N 0.000 description 1
- CTUXILQBEJGEAT-UHFFFAOYSA-N anthracene-9-thiol Chemical compound C1=CC=C2C(S)=C(C=CC=C3)C3=CC2=C1 CTUXILQBEJGEAT-UHFFFAOYSA-N 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- 125000005427 anthranyl group Chemical group 0.000 description 1
- VEQOALNAAJBPNY-UHFFFAOYSA-N antipyrine Chemical compound CN1C(C)=CC(=O)N1C1=CC=CC=C1 VEQOALNAAJBPNY-UHFFFAOYSA-N 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000008365 aromatic ketones Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- DMLAVOWQYNRWNQ-UHFFFAOYSA-N azobenzene Chemical compound C1=CC=CC=C1N=NC1=CC=CC=C1 DMLAVOWQYNRWNQ-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- XILYOLONIFWGMT-UHFFFAOYSA-N benzene;dihydrochloride Chemical compound Cl.Cl.C1=CC=CC=C1 XILYOLONIFWGMT-UHFFFAOYSA-N 0.000 description 1
- ULKGULQGPBMIJU-UHFFFAOYSA-N benzene;hydron;bromide Chemical compound Br.C1=CC=CC=C1 ULKGULQGPBMIJU-UHFFFAOYSA-N 0.000 description 1
- DALDUXIBIKGWTK-UHFFFAOYSA-N benzene;toluene Chemical compound C1=CC=CC=C1.CC1=CC=CC=C1 DALDUXIBIKGWTK-UHFFFAOYSA-N 0.000 description 1
- VJPAMLCBTIWAHI-UHFFFAOYSA-N benzo[7]annulen-7-one Chemical compound C1=CC(=O)C=CC2=CC=CC=C21 VJPAMLCBTIWAHI-UHFFFAOYSA-N 0.000 description 1
- OXWHZARNAGLRFL-UHFFFAOYSA-N benzo[b]pyrene-1,6-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C=CC(=O)C4=C3C2=C1C=C4 OXWHZARNAGLRFL-UHFFFAOYSA-N 0.000 description 1
- XYKSABPYIZPLRX-UHFFFAOYSA-N benzo[e][1,2]benzothiazole Chemical compound C1=CC=CC2=C3C=NSC3=CC=C21 XYKSABPYIZPLRX-UHFFFAOYSA-N 0.000 description 1
- LGMRJEZNTZJDHP-UHFFFAOYSA-N benzo[e]azulene Chemical compound C1=CC2=CC=CC=C2C2=CC=CC2=C1 LGMRJEZNTZJDHP-UHFFFAOYSA-N 0.000 description 1
- GDUFLCCHLCZVCJ-UHFFFAOYSA-N benzo[f][1]benzothiole-4,9-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1SC=C2 GDUFLCCHLCZVCJ-UHFFFAOYSA-N 0.000 description 1
- QGGSWEDJFFDTIQ-UHFFFAOYSA-N benzo[f][2]benzothiole Chemical compound C1=CC=CC2=CC3=CSC=C3C=C21 QGGSWEDJFFDTIQ-UHFFFAOYSA-N 0.000 description 1
- YUFRAQHYKKPYLH-UHFFFAOYSA-N benzo[f]quinoxaline Chemical compound C1=CN=C2C3=CC=CC=C3C=CC2=N1 YUFRAQHYKKPYLH-UHFFFAOYSA-N 0.000 description 1
- RGBMMOMUOWOGBF-UHFFFAOYSA-N benzo[g][2,1]benzothiazole Chemical compound C1=CC=C2C3=NSC=C3C=CC2=C1 RGBMMOMUOWOGBF-UHFFFAOYSA-N 0.000 description 1
- YPEFMQGGABUYFX-UHFFFAOYSA-N benzo[g][2]benzothiole Chemical compound C1=CC=C2C3=CSC=C3C=CC2=C1 YPEFMQGGABUYFX-UHFFFAOYSA-N 0.000 description 1
- WARCRYXKINZHGQ-UHFFFAOYSA-N benzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1 WARCRYXKINZHGQ-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- MNRAIQRGNRYJHM-UHFFFAOYSA-N benzoic acid;2,3,5,6-tetrachlorobenzene-1,4-diol Chemical compound OC(=O)C1=CC=CC=C1.OC1=C(Cl)C(Cl)=C(O)C(Cl)=C1Cl MNRAIQRGNRYJHM-UHFFFAOYSA-N 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- 150000004054 benzoquinones Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229940093265 berberine Drugs 0.000 description 1
- 229960002045 bergapten Drugs 0.000 description 1
- KGZDKFWCIPZMRK-UHFFFAOYSA-N bergapten Natural products COC1C2=C(Cc3ccoc13)C=CC(=O)O2 KGZDKFWCIPZMRK-UHFFFAOYSA-N 0.000 description 1
- 229950011260 betanaphthol Drugs 0.000 description 1
- QBUVFDKTZJNUPP-UHFFFAOYSA-N biliverdin-IXalpha Natural products N1C(=O)C(C)=C(C=C)C1=CC1=C(C)C(CCC(O)=O)=C(C=C2C(=C(C)C(C=C3C(=C(C=C)C(=O)N3)C)=N2)CCC(O)=O)N1 QBUVFDKTZJNUPP-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical group C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- LXAHJTLFCWQKCR-UHFFFAOYSA-N but-3-enylcyclohexane Chemical compound C=CCCC1CCCCC1 LXAHJTLFCWQKCR-UHFFFAOYSA-N 0.000 description 1
- IRXBNHGNHKNOJI-UHFFFAOYSA-N butanedioyl dichloride Chemical compound ClC(=O)CCC(Cl)=O IRXBNHGNHKNOJI-UHFFFAOYSA-N 0.000 description 1
- 150000004648 butanoic acid derivatives Chemical class 0.000 description 1
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- VZTUIEROBZXUFA-UHFFFAOYSA-N canadine Chemical compound C1=C2C3CC4=CC=C(OC)C(OC)=C4CN3CCC2=CC2=C1OCO2 VZTUIEROBZXUFA-UHFFFAOYSA-N 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001716 carbazoles Chemical class 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229950005499 carbon tetrachloride Drugs 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N carbostyril Natural products C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 229960001701 chloroform Drugs 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 229930002868 chlorophyll a Natural products 0.000 description 1
- NSMUHPMZFPKNMZ-VBYMZDBQSA-M chlorophyll b Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C=O)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 NSMUHPMZFPKNMZ-VBYMZDBQSA-M 0.000 description 1
- 229930002869 chlorophyll b Natural products 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 229940107161 cholesterol Drugs 0.000 description 1
- QZHPTGXQGDFGEN-UHFFFAOYSA-N chromene Chemical compound C1=CC=C2C=C[CH]OC2=C1 QZHPTGXQGDFGEN-UHFFFAOYSA-N 0.000 description 1
- 150000008371 chromenes Chemical class 0.000 description 1
- MCDZAXCSYDQTAB-UHFFFAOYSA-N chromenol Natural products CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCC1(C)Oc2ccc(O)cc2C=C1)C)C)C)C)C)C MCDZAXCSYDQTAB-UHFFFAOYSA-N 0.000 description 1
- OTAFHZMPRISVEM-UHFFFAOYSA-N chromone Chemical compound C1=CC=C2C(=O)C=COC2=C1 OTAFHZMPRISVEM-UHFFFAOYSA-N 0.000 description 1
- DODZTSARNRLOKY-UHFFFAOYSA-N cinnolin-4-amine Chemical compound C1=CC=C2C(N)=CN=NC2=C1 DODZTSARNRLOKY-UHFFFAOYSA-N 0.000 description 1
- WCZVZNOTHYJIEI-UHFFFAOYSA-N cinnoline Chemical compound N1=NC=CC2=CC=CC=C21 WCZVZNOTHYJIEI-UHFFFAOYSA-N 0.000 description 1
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cis-cyclohexene Natural products C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 1
- 229960001338 colchicine Drugs 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- GLNDAGDHSLMOKX-UHFFFAOYSA-N coumarin 120 Chemical compound C1=C(N)C=CC2=C1OC(=O)C=C2C GLNDAGDHSLMOKX-UHFFFAOYSA-N 0.000 description 1
- CEJANLKHJMMNQB-UHFFFAOYSA-M cryptocyanin Chemical compound [I-].C12=CC=CC=C2N(CC)C=CC1=CC=CC1=CC=[N+](CC)C2=CC=CC=C12 CEJANLKHJMMNQB-UHFFFAOYSA-M 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 description 1
- VEVZSMAEJFVWIL-UHFFFAOYSA-O cyanidin cation Chemical compound [O+]=1C2=CC(O)=CC(O)=C2C=C(O)C=1C1=CC=C(O)C(O)=C1 VEVZSMAEJFVWIL-UHFFFAOYSA-O 0.000 description 1
- LNDJVIYUJOJFSO-UHFFFAOYSA-N cyanoacetylene Chemical group C#CC#N LNDJVIYUJOJFSO-UHFFFAOYSA-N 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- ZYRKBGIIBMTQHN-UHFFFAOYSA-N cyclodecapentaene Chemical compound C1=CC=CC=CC=CC=C1 ZYRKBGIIBMTQHN-UHFFFAOYSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
- ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical compound C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohexene oxide Natural products O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- KIRQMGOOUCTVMV-UHFFFAOYSA-N cyclohexyl ethaneperoxoate Chemical compound CC(=O)OOC1CCCCC1 KIRQMGOOUCTVMV-UHFFFAOYSA-N 0.000 description 1
- WXAYGJXNCLBUDJ-UHFFFAOYSA-N cyclooctadecanone Chemical compound O=C1CCCCCCCCCCCCCCCCC1 WXAYGJXNCLBUDJ-UHFFFAOYSA-N 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical group C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- IYGYMKDQCDOMRE-UHFFFAOYSA-N d-Bicucullin Natural products CN1CCC2=CC=3OCOC=3C=C2C1C1OC(=O)C2=C1C=CC1=C2OCO1 IYGYMKDQCDOMRE-UHFFFAOYSA-N 0.000 description 1
- 229960001577 dantron Drugs 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- AQEFLFZSWDEAIP-UHFFFAOYSA-N di-tert-butyl ether Chemical compound CC(C)(C)OC(C)(C)C AQEFLFZSWDEAIP-UHFFFAOYSA-N 0.000 description 1
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 1
- 229910000071 diazene Inorganic materials 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- LHRCREOYAASXPZ-UHFFFAOYSA-N dibenz[a,h]anthracene Chemical compound C1=CC=C2C(C=C3C=CC=4C(C3=C3)=CC=CC=4)=C3C=CC2=C1 LHRCREOYAASXPZ-UHFFFAOYSA-N 0.000 description 1
- MMSPDYSXIHHWTH-UHFFFAOYSA-N dibenzothiophene-2,8-diamine Chemical compound C1=C(N)C=C2C3=CC(N)=CC=C3SC2=C1 MMSPDYSXIHHWTH-UHFFFAOYSA-N 0.000 description 1
- DOBMPNYZJYQDGZ-UHFFFAOYSA-N dicoumarol Chemical compound C1=CC=CC2=C1OC(=O)C(CC=1C(OC3=CC=CC=C3C=1O)=O)=C2O DOBMPNYZJYQDGZ-UHFFFAOYSA-N 0.000 description 1
- 229960001912 dicoumarol Drugs 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 229940120503 dihydroxyacetone Drugs 0.000 description 1
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical compound O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- CJSBUWDGPXGFGA-UHFFFAOYSA-N dimethyl-butadiene Natural products CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 1
- UBHZUDXTHNMNLD-UHFFFAOYSA-N dimethylsilane Chemical compound C[SiH2]C UBHZUDXTHNMNLD-UHFFFAOYSA-N 0.000 description 1
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- CHYUXCABJMXHJN-UHFFFAOYSA-N diphenyl(sulfanylidene)phosphanium Chemical compound C=1C=CC=CC=1[P+](=S)C1=CC=CC=C1 CHYUXCABJMXHJN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- FGXWKSZFVQUSTL-UHFFFAOYSA-N domperidone Chemical compound C12=CC=CC=C2NC(=O)N1CCCN(CC1)CCC1N1C2=CC=C(Cl)C=C2NC1=O FGXWKSZFVQUSTL-UHFFFAOYSA-N 0.000 description 1
- FWKBXSPDFCAHFN-DEOSSOPVSA-N dracorubin Chemical compound C1([C@H]2OC=3C=4C=5C=C(OC6=CC(=O)C(C)=C(C=56)OC=4C=C(C=3CC2)OC)C=2C=CC=CC=2)=CC=CC=C1 FWKBXSPDFCAHFN-DEOSSOPVSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229960003399 estrone Drugs 0.000 description 1
- YTNSORHOXXXTHX-UHFFFAOYSA-N ethene perylene Chemical group C=C.C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 YTNSORHOXXXTHX-UHFFFAOYSA-N 0.000 description 1
- AZDCYKCDXXPQIK-UHFFFAOYSA-N ethenoxymethylbenzene Chemical compound C=COCC1=CC=CC=C1 AZDCYKCDXXPQIK-UHFFFAOYSA-N 0.000 description 1
- YCUBDDIKWLELPD-UHFFFAOYSA-N ethenyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC=C YCUBDDIKWLELPD-UHFFFAOYSA-N 0.000 description 1
- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
- WNMORWGTPVWAIB-UHFFFAOYSA-N ethenyl 2-methylpropanoate Chemical compound CC(C)C(=O)OC=C WNMORWGTPVWAIB-UHFFFAOYSA-N 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- UJRIYYLGNDXVTA-UHFFFAOYSA-N ethenyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC=C UJRIYYLGNDXVTA-UHFFFAOYSA-N 0.000 description 1
- LZWYWAIOTBEZFN-UHFFFAOYSA-N ethenyl hexanoate Chemical compound CCCCCC(=O)OC=C LZWYWAIOTBEZFN-UHFFFAOYSA-N 0.000 description 1
- NCHRDVARPJUMRC-UHFFFAOYSA-N ethenyl methyl carbonate Chemical compound COC(=O)OC=C NCHRDVARPJUMRC-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- VEWLDLAARDMXSB-UHFFFAOYSA-N ethenyl sulfate;hydron Chemical compound OS(=O)(=O)OC=C VEWLDLAARDMXSB-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- XKHPEMKBJGUYCM-UHFFFAOYSA-N ethyl 2-oxochromene-3-carboxylate Chemical compound C1=CC=C2OC(=O)C(C(=O)OCC)=CC2=C1 XKHPEMKBJGUYCM-UHFFFAOYSA-N 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 229940035423 ethyl ether Drugs 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 229940117360 ethyl pyruvate Drugs 0.000 description 1
- BFUWRLFOXRAWGF-UHFFFAOYSA-N ethylsulfanylformic acid Chemical compound CCSC(O)=O BFUWRLFOXRAWGF-UHFFFAOYSA-N 0.000 description 1
- BUMHLZPAQKNDBJ-JTQLQIEISA-N euparin Natural products CC=C[C@H]1Cc2cc(C(=O)C)c(O)cc2O1 BUMHLZPAQKNDBJ-JTQLQIEISA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- XHEFDIBZLJXQHF-UHFFFAOYSA-N fisetin Chemical compound C=1C(O)=CC=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 XHEFDIBZLJXQHF-UHFFFAOYSA-N 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 150000002212 flavone derivatives Chemical class 0.000 description 1
- 150000002213 flavones Chemical class 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- GANXFQTZEVGPPI-UHFFFAOYSA-N fluorosulfonyloxyethene Chemical compound FS(=O)(=O)OC=C GANXFQTZEVGPPI-UHFFFAOYSA-N 0.000 description 1
- YEQFXLJGRXZCFU-UHFFFAOYSA-N formaldehyde;4-methylbenzenesulfonamide Chemical compound O=C.CC1=CC=C(S(N)(=O)=O)C=C1 YEQFXLJGRXZCFU-UHFFFAOYSA-N 0.000 description 1
- CNUDBTRUORMMPA-UHFFFAOYSA-N formylthiophene Chemical compound O=CC1=CC=CS1 CNUDBTRUORMMPA-UHFFFAOYSA-N 0.000 description 1
- XEOSBIMHSUFHQH-UHFFFAOYSA-N fulvalene Chemical compound C1=CC=CC1=C1C=CC=C1 XEOSBIMHSUFHQH-UHFFFAOYSA-N 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 150000002238 fumaric acids Chemical class 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940096919 glycogen Drugs 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229920000588 gutta-percha Polymers 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 0.000 description 1
- KDEZIUOWTXJEJK-UHFFFAOYSA-N heptacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC6=CC7=CC=CC=C7C=C6C=C5C=C4C=C3C=C21 KDEZIUOWTXJEJK-UHFFFAOYSA-N 0.000 description 1
- DDTGNKBZWQHIEH-UHFFFAOYSA-N heptalene Chemical compound C1=CC=CC=C2C=CC=CC=C21 DDTGNKBZWQHIEH-UHFFFAOYSA-N 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- QSQIGGCOCHABAP-UHFFFAOYSA-N hexacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC6=CC=CC=C6C=C5C=C4C=C3C=C21 QSQIGGCOCHABAP-UHFFFAOYSA-N 0.000 description 1
- PMYUVOOOQDGQNW-UHFFFAOYSA-N hexasodium;trioxido(trioxidosilyloxy)silane Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])O[Si]([O-])([O-])[O-] PMYUVOOOQDGQNW-UHFFFAOYSA-N 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- PFOARMALXZGCHY-UHFFFAOYSA-N homoegonol Natural products C1=C(OC)C(OC)=CC=C1C1=CC2=CC(CCCO)=CC(OC)=C2O1 PFOARMALXZGCHY-UHFFFAOYSA-N 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- JBFYUZGYRGXSFL-UHFFFAOYSA-N imidazolide Chemical compound C1=C[N-]C=N1 JBFYUZGYRGXSFL-UHFFFAOYSA-N 0.000 description 1
- QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical compound C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 150000002475 indoles Chemical class 0.000 description 1
- CGCYNUCJTZKIJR-UHFFFAOYSA-N indolo[1,2-c]quinazoline Chemical compound N12C=NC3=CC=C[CH]C3=C2C=C2[C]1C=CC=C2 CGCYNUCJTZKIJR-UHFFFAOYSA-N 0.000 description 1
- RSAZYXZUJROYKR-UHFFFAOYSA-N indophenol Chemical compound C1=CC(O)=CC=C1N=C1C=CC(=O)C=C1 RSAZYXZUJROYKR-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- ZTKMNYDOFAYRAK-UHFFFAOYSA-N isoacronycine Natural products CN1C2=CC=CC=C2C(=O)C2=C1C=C1OC(C)(C)C=CC1=C2OC ZTKMNYDOFAYRAK-UHFFFAOYSA-N 0.000 description 1
- 125000003151 isocoumarinyl group Chemical class C1(=O)OC(=CC2=CC=CC=C12)* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- WARQUFORVQESFF-UHFFFAOYSA-N isocyanatoethene Chemical compound C=CN=C=O WARQUFORVQESFF-UHFFFAOYSA-N 0.000 description 1
- 229930012930 isoflavone derivative Natural products 0.000 description 1
- 150000002515 isoflavone derivatives Chemical class 0.000 description 1
- 150000002518 isoindoles Chemical class 0.000 description 1
- OSILBMSORKFRTB-UHFFFAOYSA-N isoquinolin-1-amine Chemical compound C1=CC=C2C(N)=NC=CC2=C1 OSILBMSORKFRTB-UHFFFAOYSA-N 0.000 description 1
- HJHXYSBRTVFEDD-UHFFFAOYSA-N isoquinoline-1-carbonitrile Chemical compound C1=CC=C2C(C#N)=NC=CC2=C1 HJHXYSBRTVFEDD-UHFFFAOYSA-N 0.000 description 1
- 150000002545 isoxazoles Chemical class 0.000 description 1
- IYRMWMYZSQPJKC-UHFFFAOYSA-N kaempferol Chemical compound C1=CC(O)=CC=C1C1=C(O)C(=O)C2=C(O)C=C(O)C=C2O1 IYRMWMYZSQPJKC-UHFFFAOYSA-N 0.000 description 1
- KGPAYJZAMGEDIQ-UHFFFAOYSA-N laudanosine Natural products C1=C(OC)C(OC)=CC=C1CC1C2=CC(OC)=C(OC)C=C2CCN1C KGPAYJZAMGEDIQ-UHFFFAOYSA-N 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- OCWMFVJKFWXKNZ-UHFFFAOYSA-L lead(2+);oxygen(2-);sulfate Chemical compound [O-2].[O-2].[O-2].[Pb+2].[Pb+2].[Pb+2].[Pb+2].[O-]S([O-])(=O)=O OCWMFVJKFWXKNZ-UHFFFAOYSA-L 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 108010003491 maclurin Proteins 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Inorganic materials O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 1
- DCUFMVPCXCSVNP-UHFFFAOYSA-N methacrylic anhydride Chemical compound CC(=C)C(=O)OC(=O)C(C)=C DCUFMVPCXCSVNP-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 1
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 1
- 229940012189 methyl orange Drugs 0.000 description 1
- CEQFOVLGLXCDCX-WUKNDPDISA-N methyl red Chemical compound C1=CC(N(C)C)=CC=C1\N=N\C1=CC=CC=C1C(O)=O CEQFOVLGLXCDCX-WUKNDPDISA-N 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- SAWKFRBJGLMMES-UHFFFAOYSA-N methylphosphine Chemical compound PC SAWKFRBJGLMMES-UHFFFAOYSA-N 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- GFWPWSNIXRDQJC-UHFFFAOYSA-N morrelloflavone Natural products C1=CC(O)=CC=C1C1C(C=2C3=C(C(C=C(O3)C=3C=C(O)C(O)=CC=3)=O)C(O)=CC=2O)C(=O)C2=C(O)C=C(O)C=C2O1 GFWPWSNIXRDQJC-UHFFFAOYSA-N 0.000 description 1
- QAOHUQQBIYCWLD-UHFFFAOYSA-N n,n'-dibutylmethanediimine Chemical compound CCCCN=C=NCCCC QAOHUQQBIYCWLD-UHFFFAOYSA-N 0.000 description 1
- UHAAFJWANJYDIS-UHFFFAOYSA-N n,n'-diethylmethanediimine Chemical compound CCN=C=NCC UHAAFJWANJYDIS-UHFFFAOYSA-N 0.000 description 1
- TXOUDPQJASQYBZ-UHFFFAOYSA-N n,n'-dihexylmethanediimine Chemical compound CCCCCCN=C=NCCCCCC TXOUDPQJASQYBZ-UHFFFAOYSA-N 0.000 description 1
- CMESPBFFDMPSIY-UHFFFAOYSA-N n,n'-diphenylmethanediimine Chemical compound C1=CC=CC=C1N=C=NC1=CC=CC=C1 CMESPBFFDMPSIY-UHFFFAOYSA-N 0.000 description 1
- SHXOKQKTZJXHHR-UHFFFAOYSA-N n,n-diethyl-5-iminobenzo[a]phenoxazin-9-amine;hydrochloride Chemical compound [Cl-].C1=CC=C2C3=NC4=CC=C(N(CC)CC)C=C4OC3=CC(=[NH2+])C2=C1 SHXOKQKTZJXHHR-UHFFFAOYSA-N 0.000 description 1
- JBHJUPSXUYRTPU-UHFFFAOYSA-N n,n-dimethylanthracen-2-amine Chemical compound C1=CC=CC2=CC3=CC(N(C)C)=CC=C3C=C21 JBHJUPSXUYRTPU-UHFFFAOYSA-N 0.000 description 1
- XXTISPYPIAPDGY-UHFFFAOYSA-N n,n-diphenylmethanimidamide Chemical compound C=1C=CC=CC=1N(C=N)C1=CC=CC=C1 XXTISPYPIAPDGY-UHFFFAOYSA-N 0.000 description 1
- DIZIHZIDOWAXHD-UHFFFAOYSA-N n-(1,4-dioxonaphthalen-2-yl)nitrous amide Chemical compound C1=CC=C2C(=O)C(NN=O)=CC(=O)C2=C1 DIZIHZIDOWAXHD-UHFFFAOYSA-N 0.000 description 1
- YFZFXBKXXAVGIB-UHFFFAOYSA-N n-(3-chloro-1,4-dioxonaphthalen-2-yl)-n-(4-methylphenyl)nitrous amide Chemical compound C1=CC(C)=CC=C1N(N=O)C1=C(Cl)C(=O)C2=CC=CC=C2C1=O YFZFXBKXXAVGIB-UHFFFAOYSA-N 0.000 description 1
- GCEKYTPKZPOBRL-UHFFFAOYSA-N n-(7-chloro-5,8-dioxo-6-phenylnaphthalen-1-yl)nitrous amide Chemical compound O=C1C2=CC=CC(NN=O)=C2C(=O)C(Cl)=C1C1=CC=CC=C1 GCEKYTPKZPOBRL-UHFFFAOYSA-N 0.000 description 1
- RBHDHUYOZLKADU-UHFFFAOYSA-N n-benzylnaphthalen-1-amine Chemical compound C=1C=CC2=CC=CC=C2C=1NCC1=CC=CC=C1 RBHDHUYOZLKADU-UHFFFAOYSA-N 0.000 description 1
- HNHVTXYLRVGMHD-UHFFFAOYSA-N n-butyl isocyanate Chemical compound CCCCN=C=O HNHVTXYLRVGMHD-UHFFFAOYSA-N 0.000 description 1
- KDFFXYVOTKKBDI-UHFFFAOYSA-N n-ethylnaphthalen-1-amine Chemical compound C1=CC=C2C(NCC)=CC=CC2=C1 KDFFXYVOTKKBDI-UHFFFAOYSA-N 0.000 description 1
- IAFPDMZRLPCYAB-UHFFFAOYSA-N n-hydroxy-n-naphthalen-1-ylnitrous amide Chemical compound C1=CC=C2C(N(N=O)O)=CC=CC2=C1 IAFPDMZRLPCYAB-UHFFFAOYSA-N 0.000 description 1
- XQMQIMWCQMZJMX-UHFFFAOYSA-N n-methylanthracen-9-amine Chemical compound C1=CC=C2C(NC)=C(C=CC=C3)C3=CC2=C1 XQMQIMWCQMZJMX-UHFFFAOYSA-N 0.000 description 1
- AKEYUWUEAXIBTF-UHFFFAOYSA-N n-methylnaphthalen-1-amine Chemical compound C1=CC=C2C(NC)=CC=CC2=C1 AKEYUWUEAXIBTF-UHFFFAOYSA-N 0.000 description 1
- JKWBKJBGDIARCA-UHFFFAOYSA-N n-naphthalen-1-yl-n-nitronitramide Chemical compound C1=CC=C2C(N([N+](=O)[O-])[N+]([O-])=O)=CC=CC2=C1 JKWBKJBGDIARCA-UHFFFAOYSA-N 0.000 description 1
- VCCSDHQQJGGZHD-UHFFFAOYSA-N n-naphthalen-1-ylcarbamoyl chloride Chemical compound C1=CC=C2C(NC(=O)Cl)=CC=CC2=C1 VCCSDHQQJGGZHD-UHFFFAOYSA-N 0.000 description 1
- XSCFKJGIAYKLRV-UHFFFAOYSA-N n-naphthalen-1-ylnitramide Chemical compound C1=CC=C2C(N[N+](=O)[O-])=CC=CC2=C1 XSCFKJGIAYKLRV-UHFFFAOYSA-N 0.000 description 1
- FVDWCUCFCUDCRO-UHFFFAOYSA-N n-naphthalen-2-ylnitrous amide Chemical compound C1=CC=CC2=CC(NN=O)=CC=C21 FVDWCUCFCUDCRO-UHFFFAOYSA-N 0.000 description 1
- LNVQBBHYPGFSMX-UHFFFAOYSA-N n-phenylacridin-9-amine Chemical compound C=12C=CC=CC2=NC2=CC=CC=C2C=1NC1=CC=CC=C1 LNVQBBHYPGFSMX-UHFFFAOYSA-N 0.000 description 1
- BIWQNAUHSWTLBO-UHFFFAOYSA-N n-phenylanthracen-2-amine Chemical compound C=1C=C2C=C3C=CC=CC3=CC2=CC=1NC1=CC=CC=C1 BIWQNAUHSWTLBO-UHFFFAOYSA-N 0.000 description 1
- CIPHTOQKGSLCLV-UHFFFAOYSA-N n-phenylnaphthalene-1-carboxamide Chemical compound C=1C=CC2=CC=CC=C2C=1C(=O)NC1=CC=CC=C1 CIPHTOQKGSLCLV-UHFFFAOYSA-N 0.000 description 1
- 150000004002 naphthaldehydes Chemical class 0.000 description 1
- QFVRQPUZNPEPGA-UHFFFAOYSA-N naphthalen-1-yl(diphenyl)methanol Chemical compound C=1C=CC=CC=1C(C=1C2=CC=CC=C2C=CC=1)(O)C1=CC=CC=C1 QFVRQPUZNPEPGA-UHFFFAOYSA-N 0.000 description 1
- STUPJDVVIONFLI-UHFFFAOYSA-N naphthalen-1-yl(phenyl)methanol Chemical compound C=1C=CC2=CC=CC=C2C=1C(O)C1=CC=CC=C1 STUPJDVVIONFLI-UHFFFAOYSA-N 0.000 description 1
- NVSYANRBXPURRQ-UHFFFAOYSA-N naphthalen-1-ylmethanamine Chemical compound C1=CC=C2C(CN)=CC=CC2=C1 NVSYANRBXPURRQ-UHFFFAOYSA-N 0.000 description 1
- FVSUYFWWFUVGRG-UHFFFAOYSA-N naphthalen-1-ylurea Chemical compound C1=CC=C2C(NC(=O)N)=CC=CC2=C1 FVSUYFWWFUVGRG-UHFFFAOYSA-N 0.000 description 1
- MXNXGPHHIUHJRF-UHFFFAOYSA-N naphthalene-1,2,3,4-tetramine Chemical compound C1=CC=CC2=C(N)C(N)=C(N)C(N)=C21 MXNXGPHHIUHJRF-UHFFFAOYSA-N 0.000 description 1
- WMPJPAMWRAOQSU-UHFFFAOYSA-N naphthalene-1,2-dicarbaldehyde Chemical compound C1=CC=CC2=C(C=O)C(C=O)=CC=C21 WMPJPAMWRAOQSU-UHFFFAOYSA-N 0.000 description 1
- AAPAGLBSROJFGM-UHFFFAOYSA-N naphthalene-1,5-dithiol Chemical compound C1=CC=C2C(S)=CC=CC2=C1S AAPAGLBSROJFGM-UHFFFAOYSA-N 0.000 description 1
- YJMNOKOLADGBKA-UHFFFAOYSA-N naphthalene-1-carbonitrile Chemical compound C1=CC=C2C(C#N)=CC=CC2=C1 YJMNOKOLADGBKA-UHFFFAOYSA-N 0.000 description 1
- RMHJJUOPOWPRBP-UHFFFAOYSA-N naphthalene-1-carboxamide Chemical compound C1=CC=C2C(C(=O)N)=CC=CC2=C1 RMHJJUOPOWPRBP-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- SLBHRPOLVUEFSG-UHFFFAOYSA-N naphthalene-2,6-dione Chemical compound O=C1C=CC2=CC(=O)C=CC2=C1 SLBHRPOLVUEFSG-UHFFFAOYSA-N 0.000 description 1
- IHRUNHAGYIHWNV-UHFFFAOYSA-N naphtho[2,3-h]cinnoline Chemical compound C1=NN=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 IHRUNHAGYIHWNV-UHFFFAOYSA-N 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- PGSADBUBUOPOJS-UHFFFAOYSA-N neutral red Chemical compound Cl.C1=C(C)C(N)=CC2=NC3=CC(N(C)C)=CC=C3N=C21 PGSADBUBUOPOJS-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 150000002832 nitroso derivatives Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- LSQODMMMSXHVCN-UHFFFAOYSA-N ovalene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3C5=C6C(C=C3)=CC=C3C6=C6C(C=C3)=C3)C4=C5C6=C2C3=C1 LSQODMMMSXHVCN-UHFFFAOYSA-N 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- DTHHUAXKOMWYBI-UHFFFAOYSA-N oxadiazolidine Chemical compound C1CONN1 DTHHUAXKOMWYBI-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 150000002916 oxazoles Chemical class 0.000 description 1
- ATYBXHSAIOKLMG-UHFFFAOYSA-N oxepin Chemical compound O1C=CC=CC=C1 ATYBXHSAIOKLMG-UHFFFAOYSA-N 0.000 description 1
- WKGDNXBDNLZSKC-UHFFFAOYSA-N oxido(phenyl)phosphanium Chemical compound O=[PH2]c1ccccc1 WKGDNXBDNLZSKC-UHFFFAOYSA-N 0.000 description 1
- 229960003625 oxolamine Drugs 0.000 description 1
- HDBWAWNLGGMZRQ-UHFFFAOYSA-N p-Vinylbiphenyl Chemical group C1=CC(C=C)=CC=C1C1=CC=CC=C1 HDBWAWNLGGMZRQ-UHFFFAOYSA-N 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 229960001789 papaverine Drugs 0.000 description 1
- AFAIELJLZYUNPW-UHFFFAOYSA-N pararosaniline free base Chemical compound C1=CC(N)=CC=C1C(C=1C=CC(N)=CC=1)=C1C=CC(=N)C=C1 AFAIELJLZYUNPW-UHFFFAOYSA-N 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- RQPUZGKLFDPSJD-UHFFFAOYSA-N pent-1-enylcyclohexane Chemical compound CCCC=CC1CCCCC1 RQPUZGKLFDPSJD-UHFFFAOYSA-N 0.000 description 1
- SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 description 1
- JKPCLJPYZMKPHM-UHFFFAOYSA-N pentahelicene Chemical compound C1=CC=C2C3=C4C5=CC=CC=C5C=CC4=CC=C3C=CC2=C1 JKPCLJPYZMKPHM-UHFFFAOYSA-N 0.000 description 1
- JZRYQZJSTWVBBD-UHFFFAOYSA-N pentaporphyrin i Chemical compound N1C(C=C2NC(=CC3=NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 JZRYQZJSTWVBBD-UHFFFAOYSA-N 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- XDJOIMJURHQYDW-UHFFFAOYSA-N phenalene Chemical compound C1=CC(CC=C2)=C3C2=CC=CC3=C1 XDJOIMJURHQYDW-UHFFFAOYSA-N 0.000 description 1
- KYFGEYPMYUNWFP-UHFFFAOYSA-N phenanthren-1-yl(phenyl)methanone Chemical compound C=1C=CC(C2=CC=CC=C2C=C2)=C2C=1C(=O)C1=CC=CC=C1 KYFGEYPMYUNWFP-UHFFFAOYSA-N 0.000 description 1
- SCOAVUHOIJMIBW-UHFFFAOYSA-N phenanthrene-1,2-dione Chemical compound C1=CC=C2C(C=CC(C3=O)=O)=C3C=CC2=C1 SCOAVUHOIJMIBW-UHFFFAOYSA-N 0.000 description 1
- POZPGRADIOPGIR-UHFFFAOYSA-N phenanthrene-1,4-dione Chemical compound C1=CC2=CC=CC=C2C2=C1C(=O)C=CC2=O POZPGRADIOPGIR-UHFFFAOYSA-N 0.000 description 1
- NKGGYWQZHFAHRK-UHFFFAOYSA-N phenanthrene-3,4-dione Chemical compound C1=CC=CC2=C(C(C(=O)C=C3)=O)C3=CC=C21 NKGGYWQZHFAHRK-UHFFFAOYSA-N 0.000 description 1
- 150000002987 phenanthrenes Chemical class 0.000 description 1
- 229960005222 phenazone Drugs 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- BSCCSDNZEIHXOK-UHFFFAOYSA-N phenyl carbamate Chemical compound NC(=O)OC1=CC=CC=C1 BSCCSDNZEIHXOK-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- CSITWAJZNCHZGS-UHFFFAOYSA-N phenyl-(2-phenyl-1H-indol-3-yl)diazene Chemical compound c1ccc(cc1)N=Nc1c([nH]c2ccccc12)-c1ccccc1 CSITWAJZNCHZGS-UHFFFAOYSA-N 0.000 description 1
- ZBVQEUUTPTVMHY-UHFFFAOYSA-N phenyl-(2-phenylphenyl)methanone Chemical compound C=1C=CC=C(C=2C=CC=CC=2)C=1C(=O)C1=CC=CC=C1 ZBVQEUUTPTVMHY-UHFFFAOYSA-N 0.000 description 1
- WBZKJWFHFKJJOU-UHFFFAOYSA-N phenyl-(4,4,6,6-tetramethylcyclohex-2-en-1-yl)methanone Chemical compound CC1(C(C(=O)C2=CC=CC=C2)C=CC(C1)(C)C)C WBZKJWFHFKJJOU-UHFFFAOYSA-N 0.000 description 1
- RPGWZZNNEUHDAQ-UHFFFAOYSA-N phenylphosphine Chemical compound PC1=CC=CC=C1 RPGWZZNNEUHDAQ-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical compound NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
- 229940061584 phosphoramidic acid Drugs 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- LFSXCDWNBUNEEM-UHFFFAOYSA-N phthalazine Chemical compound C1=NN=CC2=CC=CC=C21 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- MBWXNTAXLNYFJB-NKFFZRIASA-N phylloquinone Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CCC[C@H](C)CCC[C@H](C)CCCC(C)C)=C(C)C(=O)C2=C1 MBWXNTAXLNYFJB-NKFFZRIASA-N 0.000 description 1
- MBWXNTAXLNYFJB-LKUDQCMESA-N phylloquinone Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CCCC(C)CCCC(C)CCCC(C)C)=C(C)C(=O)C2=C1 MBWXNTAXLNYFJB-LKUDQCMESA-N 0.000 description 1
- SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 description 1
- 235000019175 phylloquinone Nutrition 0.000 description 1
- 239000011772 phylloquinone Substances 0.000 description 1
- 229960001898 phytomenadione Drugs 0.000 description 1
- DVDDCKBJLHNFTJ-UHFFFAOYSA-N picene-5,6-dione Chemical compound C12=CC=CC=C2C(=O)C(=O)C2=C1C=CC1=C2C=CC2=CC=CC=C12 DVDDCKBJLHNFTJ-UHFFFAOYSA-N 0.000 description 1
- QWYZFXLSWMXLDM-UHFFFAOYSA-M pinacyanol iodide Chemical compound [I-].C1=CC2=CC=CC=C2N(CC)C1=CC=CC1=CC=C(C=CC=C2)C2=[N+]1CC QWYZFXLSWMXLDM-UHFFFAOYSA-M 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001597 poly(4-chlorostyrene) Polymers 0.000 description 1
- 229920002939 poly(N,N-dimethylacrylamides) Polymers 0.000 description 1
- 229920001584 poly(acrylomorpholines) Polymers 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000052 poly(p-xylylene) Polymers 0.000 description 1
- 229920000917 poly(propylene sulfide) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 229920003251 poly(α-methylstyrene) Polymers 0.000 description 1
- 229920001197 polyacetylene Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920002577 polybenzoxazole Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002338 polyhydroxyethylmethacrylate Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229940045916 polymetaphosphate Drugs 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 108010082974 polysarcosine Proteins 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- TWFGRJUTAULJPZ-USZBIXTISA-N prodigiosin Chemical compound N1=C(C)C(CCCCC)=C\C1=C/C1=NC(C=2[N]C=CC=2)=C[C]1OC TWFGRJUTAULJPZ-USZBIXTISA-N 0.000 description 1
- ARJOQCYCJMAIFR-UHFFFAOYSA-N prop-2-enoyl prop-2-enoate Chemical compound C=CC(=O)OC(=O)C=C ARJOQCYCJMAIFR-UHFFFAOYSA-N 0.000 description 1
- KIWATKANDHUUOB-UHFFFAOYSA-N propan-2-yl 2-hydroxypropanoate Chemical compound CC(C)OC(=O)C(C)O KIWATKANDHUUOB-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- GDISDVBCNPLSDU-UHFFFAOYSA-N pyrido[2,3-g]quinoline Chemical compound C1=CC=NC2=CC3=CC=CN=C3C=C21 GDISDVBCNPLSDU-UHFFFAOYSA-N 0.000 description 1
- 235000008160 pyridoxine Nutrition 0.000 description 1
- 239000011677 pyridoxine Substances 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- LTIAEPYUMKCFJZ-UHFFFAOYSA-N pyrimido[4,5-b]quinoline Chemical compound N1=CN=CC2=CC3=CC=CC=C3N=C21 LTIAEPYUMKCFJZ-UHFFFAOYSA-N 0.000 description 1
- SMUQFGGVLNAIOZ-UHFFFAOYSA-N quinaldine Chemical compound C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- KXYNLLGPBDUAHW-UHFFFAOYSA-N quinolin-4-ylmethanol Chemical compound C1=CC=C2C(CO)=CC=NC2=C1 KXYNLLGPBDUAHW-UHFFFAOYSA-N 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- YHQSXWOXIHDVHQ-UHFFFAOYSA-N quinoline;hydrobromide Chemical compound [Br-].[NH+]1=CC=CC2=CC=CC=C21 YHQSXWOXIHDVHQ-UHFFFAOYSA-N 0.000 description 1
- YOWAEZWWQFSEJD-UHFFFAOYSA-N quinoxalin-2-amine Chemical compound C1=CC=CC2=NC(N)=CN=C21 YOWAEZWWQFSEJD-UHFFFAOYSA-N 0.000 description 1
- FFRYUAVNPBUEIC-UHFFFAOYSA-N quinoxalin-2-ol Chemical compound C1=CC=CC2=NC(O)=CN=C21 FFRYUAVNPBUEIC-UHFFFAOYSA-N 0.000 description 1
- LUDZVVVPVCUUBP-UHFFFAOYSA-N quinoxaline-2,3-diamine Chemical compound C1=CC=C2N=C(N)C(N)=NC2=C1 LUDZVVVPVCUUBP-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229920002477 rna polymer Polymers 0.000 description 1
- 229940043266 rosin Drugs 0.000 description 1
- OARRHUQTFTUEOS-UHFFFAOYSA-N safranin Chemical compound [Cl-].C=12C=C(N)C(C)=CC2=NC2=CC(C)=C(N)C=C2[N+]=1C1=CC=CC=C1 OARRHUQTFTUEOS-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- SRRKNRDXURUMPP-UHFFFAOYSA-N sodium disulfide Chemical compound [Na+].[Na+].[S-][S-] SRRKNRDXURUMPP-UHFFFAOYSA-N 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 1
- 229960004306 sulfadiazine Drugs 0.000 description 1
- MBDNRNMVTZADMQ-UHFFFAOYSA-N sulfolene Chemical compound O=S1(=O)CC=CC1 MBDNRNMVTZADMQ-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 229940052367 sulfur,colloidal Drugs 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940063650 terramycin Drugs 0.000 description 1
- QHSPZGZEUDEIQM-AATRIKPKSA-N tert-butyl (e)-but-2-enoate Chemical compound C\C=C\C(=O)OC(C)(C)C QHSPZGZEUDEIQM-AATRIKPKSA-N 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- POWFTOSLLWLEBN-UHFFFAOYSA-N tetrasodium;silicate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])[O-] POWFTOSLLWLEBN-UHFFFAOYSA-N 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 1
- 210000001541 thymus gland Anatomy 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
- OVZXISBUYCEVEV-UHFFFAOYSA-N trans-alpha-methylstilbene Natural products C=1C=CC=CC=1C(C)=CC1=CC=CC=C1 OVZXISBUYCEVEV-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 229960002415 trichloroethylene Drugs 0.000 description 1
- ULIAPOFMBCCSPE-UHFFFAOYSA-N tridecan-7-one Chemical compound CCCCCCC(=O)CCCCCC ULIAPOFMBCCSPE-UHFFFAOYSA-N 0.000 description 1
- 229960004453 trimethadione Drugs 0.000 description 1
- DOKTZMKBGPRAPB-UHFFFAOYSA-N trimethyl(naphthalen-1-yl)azanium Chemical class C1=CC=C2C([N+](C)(C)C)=CC=CC2=C1 DOKTZMKBGPRAPB-UHFFFAOYSA-N 0.000 description 1
- 125000005580 triphenylene group Chemical group 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- QFRYQWYZSQDFOS-UHFFFAOYSA-N verbascoside Natural products CC1OC(COC2C(O)C(COC3OC(C(O)C(O)C3O)C(=O)O)OC(Oc4cc(O)cc5OC(=CC(=O)c45)c6ccc(O)c(O)c6)C2O)C(O)C(O)C1O QFRYQWYZSQDFOS-UHFFFAOYSA-N 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/002—Scale prevention in a polymerisation reactor or its auxiliary parts
- C08F2/004—Scale prevention in a polymerisation reactor or its auxiliary parts by a prior coating on the reactor walls
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15252284A JPS6131406A (ja) | 1984-07-23 | 1984-07-23 | 塩化ビニル系重合体の製造方法 |
| JP15596784A JPS6134006A (ja) | 1984-07-26 | 1984-07-26 | 塩化ビニル系重合体の製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK358591A3 true SK358591A3 (en) | 1995-09-13 |
| SK277971B6 SK277971B6 (en) | 1995-09-13 |
Family
ID=26481418
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK3585-91A SK277971B6 (en) | 1984-07-23 | 1985-07-23 | Method of production of vinylchloride polymer |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US4757124A (OSRAM) |
| EP (1) | EP0172427B2 (OSRAM) |
| KR (1) | KR920004802B1 (OSRAM) |
| AR (1) | AR242595A1 (OSRAM) |
| AU (1) | AU578109B2 (OSRAM) |
| BG (1) | BG50388A3 (OSRAM) |
| BR (1) | BR8503491A (OSRAM) |
| CA (1) | CA1249099A (OSRAM) |
| DD (1) | DD237514B5 (OSRAM) |
| DE (1) | DE3571324D1 (OSRAM) |
| EG (1) | EG17349A (OSRAM) |
| ES (1) | ES8701201A1 (OSRAM) |
| FI (1) | FI81816C (OSRAM) |
| GR (1) | GR851794B (OSRAM) |
| HK (1) | HK71690A (OSRAM) |
| HU (1) | HU201786B (OSRAM) |
| ID (1) | ID977B (OSRAM) |
| IN (1) | IN165525B (OSRAM) |
| MX (1) | MX163186B (OSRAM) |
| NO (1) | NO165757C (OSRAM) |
| NZ (1) | NZ212815A (OSRAM) |
| PH (1) | PH20811A (OSRAM) |
| PL (1) | PL146867B1 (OSRAM) |
| PT (1) | PT80846B (OSRAM) |
| RO (1) | RO92870B (OSRAM) |
| RU (1) | RU2012565C1 (OSRAM) |
| SG (1) | SG15690G (OSRAM) |
| SK (1) | SK277971B6 (OSRAM) |
| YU (1) | YU44514B (OSRAM) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PH26338A (en) * | 1988-08-10 | 1992-04-29 | Shinetsu Chemical Co | Method of preventing polymer scale formation |
| JPH0739445B2 (ja) * | 1988-12-07 | 1995-05-01 | 信越化学工業株式会社 | 重合体スケールの付着防止方法 |
| US5068130A (en) * | 1990-10-23 | 1991-11-26 | E. I. Dupont De Nemours And Company | Inhibition of polymer formation on surfaces including vents by using an inhibitor paint |
| DE69209672T2 (de) * | 1991-01-22 | 1996-09-26 | Shinetsu Chemical Co | Beschichtungslösung zur Verhinderung von Polymeransatzbildung und Verfahren zu ihrem Gebrauch |
| JPH04370101A (ja) * | 1991-04-08 | 1992-12-22 | Shin Etsu Chem Co Ltd | 重合体スケール付着防止剤及び重合体スケールの付着防止方法 |
| US5486582A (en) * | 1991-07-03 | 1996-01-23 | Shin-Etsu Chemical Co., Ltd. | Polymer scale preventive process using a coating of chitosan salt and phenothiazine |
| DE69217327D1 (de) * | 1991-10-21 | 1997-03-20 | Shinetsu Chemical Co | Mittel zur Verhinderung von Polymerverkrustung, Polymerisationsgefäss, in dem die Verkrustung vermieden wird und Verfahren zur Herstellung von Polymeren unter Benutzung dieses Gefässes |
| US5493017A (en) * | 1992-08-14 | 1996-02-20 | The Trustees Of The University Of Pennsylvania | Ring-metalated porphyrins |
| US5817830A (en) * | 1992-08-14 | 1998-10-06 | Trustees Of The University Of Pennsylvania | Pyrrolic compounds |
| US5599924A (en) * | 1992-08-14 | 1997-02-04 | Trustees Of The University Of Pennsylvania | Electron-deficient porphyrins and processes and intermediates for preparing same |
| US5371199B1 (en) * | 1992-08-14 | 1995-12-26 | Univ Pennsylvania | Substituted porphyrins porphyrin-containing polymers and synthetic methods therefor |
| JP2678711B2 (ja) * | 1992-08-28 | 1997-11-17 | 信越化学工業株式会社 | 重合体スケール付着防止剤及びそれを使用する重合体製造方法 |
| GB9312853D0 (en) * | 1993-06-22 | 1993-08-04 | Euro Celtique Sa | Chemical compounds |
| US5607503A (en) * | 1993-09-03 | 1997-03-04 | Refract-A-Gard Pty Limited | Silica-based binder |
| JP3091355B2 (ja) * | 1993-11-16 | 2000-09-25 | 信越化学工業株式会社 | 重合体スケール付着防止剤及びそれを使用する重合体製造方法 |
| US5922751A (en) * | 1994-06-24 | 1999-07-13 | Euro-Celtique, S.A. | Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same |
| US5591776A (en) * | 1994-06-24 | 1997-01-07 | Euro-Celtique, S.A. | Pheynl or benzyl-substituted rolipram-based compounds for and method of inhibiting phosphodiesterase IV |
| EP0702033B1 (en) | 1994-09-14 | 1997-12-03 | Shin-Etsu Chemical Co., Ltd. | Process of producing vinyl chloride type polymer |
| CA2206804C (en) * | 1994-12-13 | 2002-03-19 | Euro-Celtique, S.A. | Trisubstituted thioxanthines |
| WO1996018399A1 (en) * | 1994-12-13 | 1996-06-20 | Euro-Celtique, S.A. | Aryl thioxanthines |
| US6025361A (en) * | 1994-12-13 | 2000-02-15 | Euro-Celtique, S.A. | Trisubstituted thioxanthines |
| US6166041A (en) * | 1995-10-11 | 2000-12-26 | Euro-Celtique, S.A. | 2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma |
| US6075016A (en) * | 1996-04-10 | 2000-06-13 | Euro-Celtique S.A. | 6,5-fused aromatic ring systems having enhanced phosphodiesterase IV inhibitory activity |
| IT1286525B1 (it) * | 1996-12-04 | 1998-07-15 | 3V Sigma Spa | Agenti anti-incrostazione,composizioni che li contengono e loro impiego nei processi di polimerizzazione |
| US5851988A (en) | 1997-01-15 | 1998-12-22 | Terrapin Technologies, Inc. | Nonpeptide insulin receptor agonists |
| KR20010020610A (ko) * | 1997-07-03 | 2001-03-15 | 해피 페너 ; 해리 에이치. 페너 2세 | 엔피와이 특이적 리간드 유형인 디아릴이미다졸 유도체 |
| DE69821432T2 (de) * | 1997-10-16 | 2004-12-30 | Mitsubishi Gas Chemical Co., Inc. | Packung und Destillationsverfahren zur Polymerisationsinhibierung von Vinylverbindungen |
| US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
| RU2292355C2 (ru) * | 2002-04-11 | 2007-01-27 | Акцо Нобель Н.В. | Способ нанесения средства против обрастания |
| DE10234398B4 (de) * | 2002-07-23 | 2006-07-27 | Ls-Medcap Gmbh | Beschichtungszusammensetzung für eine implantierbare medizinische Vorrichtung und Verfahren zur Beschichtung einer solchen Vorrichtung und seine Verwendung |
| US20090260767A1 (en) * | 2003-04-14 | 2009-10-22 | Every Penny Counts, Inc. | Use of hydrophobic dyes to monitor hydrophobic contaminants in a papermaking process |
| EP1553107B1 (en) * | 2004-01-07 | 2008-05-21 | Kuraray Co., Ltd. | Anti-fouling agent and method for producing the same |
| EP2581421A1 (en) | 2011-10-12 | 2013-04-17 | Ineos Europe AG | Additive |
| CN105318109A (zh) * | 2014-06-30 | 2016-02-10 | 江苏大力城电气有限公司 | 一种恒力支吊架用连接卡扣 |
| RU2699104C1 (ru) * | 2018-07-18 | 2019-09-03 | Акционерное общество Научный центр "Малотоннажная химия" | Новые флуоресцентные производные α-гидрокси-бисфосфонатов в качестве ингибиторов солеотложений и способы их получения |
| CN110252411B (zh) * | 2019-06-26 | 2022-02-08 | 江西蓝星星火有机硅有限公司 | 一种端环氧硅油生产用络合型铂催化剂及其制备方法和用途 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4814437B1 (OSRAM) * | 1969-12-15 | 1973-05-07 | ||
| DE91560C (OSRAM) * | 1970-05-07 | |||
| GB1365590A (en) * | 1972-03-09 | 1974-09-04 | Shinetsu Chemical Co | Method of suspension polymerizing vinyl chloride |
| DE2248607A1 (de) * | 1972-10-04 | 1974-04-11 | Wacker Chemie Gmbh | Verfahren zur herstellung von polyvinylhalogeniden |
| AU503273B2 (en) * | 1975-08-26 | 1979-08-30 | Imperial Chemical Industries Limited | Reactor and process for vinyl chloride polymerisation |
| GR64894B (en) * | 1977-01-25 | 1980-06-07 | Shinetsu Chemical Co | Method for the polymerization of a vinyl menomer |
| US4068059A (en) * | 1977-02-17 | 1978-01-10 | The B. F. Goodrich Company | Internally coated reaction vessel for use in olefinic polymerization |
| AU526104B2 (en) * | 1978-09-08 | 1982-12-16 | Geon Company, The | Polymerization of vinyl chloride |
| DE3061334D1 (en) | 1979-06-16 | 1983-01-20 | Beecham Group Plc | Ethanamine derivatives, their preparation and use in pharmaceutical compositions |
| JPH0138544B2 (OSRAM) | 1980-08-18 | 1989-08-15 | Goodrich Co B F | |
| JPS5761001A (en) | 1980-09-30 | 1982-04-13 | Shin Etsu Chem Co Ltd | Polymerizer |
| JPS5911303A (ja) | 1982-07-12 | 1984-01-20 | Shin Etsu Chem Co Ltd | ビニル系単量体の重合方法 |
| NO841249L (no) * | 1983-04-04 | 1984-10-05 | Shinetsu Chemical Co | Fremgangsmaate for fjerning av utfelt polymerskall paa reaktorvegger samt et middel for utfoerelse av fremgangsmaaten |
| JPS59202201A (ja) * | 1983-04-28 | 1984-11-16 | Shin Etsu Chem Co Ltd | 重合体スケ−ル付着防止剤およびそれを使用する方法 |
-
1985
- 1985-07-03 IN IN525/DEL/85A patent/IN165525B/en unknown
- 1985-07-17 CA CA000486934A patent/CA1249099A/en not_active Expired
- 1985-07-17 RO RO119582A patent/RO92870B/ro unknown
- 1985-07-17 PH PH35233A patent/PH20811A/en unknown
- 1985-07-17 YU YU1181/85A patent/YU44514B/xx unknown
- 1985-07-18 MX MX206034A patent/MX163186B/es unknown
- 1985-07-18 GR GR851794A patent/GR851794B/el unknown
- 1985-07-18 ES ES545331A patent/ES8701201A1/es not_active Expired
- 1985-07-19 DD DD27878385A patent/DD237514B5/de not_active IP Right Cessation
- 1985-07-19 AR AR85301041A patent/AR242595A1/es active
- 1985-07-20 KR KR1019850005185A patent/KR920004802B1/ko not_active Expired
- 1985-07-21 EG EG433/85A patent/EG17349A/xx active
- 1985-07-22 EP EP85109161A patent/EP0172427B2/en not_active Expired - Lifetime
- 1985-07-22 NZ NZ212815A patent/NZ212815A/xx unknown
- 1985-07-22 FI FI852857A patent/FI81816C/fi not_active IP Right Cessation
- 1985-07-22 RU SU853960627A patent/RU2012565C1/ru active
- 1985-07-22 PT PT80846A patent/PT80846B/pt not_active IP Right Cessation
- 1985-07-22 DE DE8585109161T patent/DE3571324D1/de not_active Expired
- 1985-07-22 HU HU852786A patent/HU201786B/hu not_active IP Right Cessation
- 1985-07-22 ID IDP410985A patent/ID977B/id unknown
- 1985-07-22 NO NO852907A patent/NO165757C/no not_active IP Right Cessation
- 1985-07-23 PL PL1985254652A patent/PL146867B1/pl unknown
- 1985-07-23 SK SK3585-91A patent/SK277971B6/sk unknown
- 1985-07-23 BG BG071188A patent/BG50388A3/xx unknown
- 1985-07-23 AU AU45274/85A patent/AU578109B2/en not_active Ceased
- 1985-07-23 BR BR8503491A patent/BR8503491A/pt not_active IP Right Cessation
-
1987
- 1987-07-21 US US07/076,996 patent/US4757124A/en not_active Expired - Lifetime
-
1990
- 1990-03-05 SG SG156/90A patent/SG15690G/en unknown
- 1990-09-13 HK HK716/90A patent/HK71690A/en not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SK358591A3 (en) | Method of production of vinylchloride polymer | |
| US4105839A (en) | Method for polymerizing ethylenically unsaturated monomers in order to eliminate polymer deposition | |
| CZ293434B6 (cs) | Způsob výroby polymeru polymerací monomeru s ethylenickou dvojnou vazbou | |
| US20110282065A1 (en) | Solid supported gold nanoparticles, methods of use thereof, and methods for making same | |
| CZ278591B6 (en) | Process for preparing polymer of vinyl chloride | |
| CZ278202B6 (en) | Process for preparing vinyl chloride polymer | |
| JPH0370723B2 (OSRAM) | ||
| JP2001011102A (ja) | エチレン性二重結合を有する単量体の重合体を製造する方法 | |
| PL102539B1 (pl) | Sposob polimeryzacji chlorku winylu | |
| DD237514A5 (de) | Verfahren zur Herstellung von Vinylchlorid-Polymeren | |
| CN1006386B (zh) | 氯乙烯聚合物的生产方法 | |
| EP0116951B1 (en) | Photosensitive compositions | |
| US4374966A (en) | Process for the manufacture of vinyl chloride polymers by coating polymerization vessels | |
| JPS5941443B2 (ja) | 重合体の製造方法 | |
| JP3665496B2 (ja) | エチレン性二重結合を有する単量体の重合による重合体の製造方法 | |
| JP2727402B2 (ja) | 重合体スケール付着防止剤及びそれを使用する重合体製造方法 | |
| CS203963B2 (cs) | Způsob potlačování usazování šupin polymeru na povrchu polymerační nádoby | |
| JPH05320210A (ja) | 重合体スケール付着防止剤ならびに重合体スケールの付着を防止する重合器及び重合体の製造方法 | |
| JPH08109203A (ja) | 塩化ビニル系重合体の製造方法 | |
| JPH08109202A (ja) | 重合体の製造方法 | |
| EP0102793A1 (en) | A process for removing polymer scale adhering to a polymerization vessel | |
| MXPA99001361A (en) | Procedure to produce a polymer by means of polymerization of a monomer that has a double link ethelin | |
| JPH0248162B2 (ja) | Enkabinirukeijugotainoseizohoho | |
| JPH07224101A (ja) | 重合体スケール付着防止剤及びそれを使用する重合体製造方法 |