JP2007056020A - 貯蔵安定性および酸系のための特別な適性 - Google Patents
貯蔵安定性および酸系のための特別な適性 Download PDFInfo
- Publication number
- JP2007056020A JP2007056020A JP2006224694A JP2006224694A JP2007056020A JP 2007056020 A JP2007056020 A JP 2007056020A JP 2006224694 A JP2006224694 A JP 2006224694A JP 2006224694 A JP2006224694 A JP 2006224694A JP 2007056020 A JP2007056020 A JP 2007056020A
- Authority
- JP
- Japan
- Prior art keywords
- thiourea
- composition according
- dental composition
- phenyl
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000003860 storage Methods 0.000 title claims description 11
- 239000002253 acid Substances 0.000 title claims description 10
- 239000000203 mixture Substances 0.000 claims abstract description 51
- -1 hydroperoxide compound Chemical class 0.000 claims abstract description 46
- 239000003999 initiator Substances 0.000 claims abstract description 29
- 239000005749 Copper compound Substances 0.000 claims abstract description 18
- 150000001880 copper compounds Chemical class 0.000 claims abstract description 18
- 238000002360 preparation method Methods 0.000 claims abstract description 12
- 150000001412 amines Chemical class 0.000 claims abstract description 9
- 150000003585 thioureas Chemical class 0.000 claims abstract description 8
- MHAJPDPJQMAIIY-UHFFFAOYSA-M hydroperoxide group Chemical group [O-]O MHAJPDPJQMAIIY-UHFFFAOYSA-M 0.000 claims abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract 3
- 229910052799 carbon Inorganic materials 0.000 claims abstract 3
- 239000000178 monomer Substances 0.000 claims description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 14
- 239000000945 filler Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 11
- 230000002378 acidificating effect Effects 0.000 claims description 9
- 239000000853 adhesive Substances 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 9
- 230000001070 adhesive effect Effects 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 239000005368 silicate glass Substances 0.000 claims description 5
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- 239000002131 composite material Substances 0.000 claims description 3
- YIWFBNMYFYINAD-UHFFFAOYSA-N ethenylcyclopropane Chemical compound C=CC1CC1 YIWFBNMYFYINAD-UHFFFAOYSA-N 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- XIBAZLLABMNRRJ-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene hydrogen peroxide Chemical compound OO.CC(C)C1=CC=C(C(C)C)C=C1 XIBAZLLABMNRRJ-UHFFFAOYSA-N 0.000 claims description 2
- LIZVXGBYTGTTTI-UHFFFAOYSA-N 2-[(4-methylphenyl)sulfonylamino]-2-phenylacetic acid Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(C(O)=O)C1=CC=CC=C1 LIZVXGBYTGTTTI-UHFFFAOYSA-N 0.000 claims description 2
- 229910052788 barium Inorganic materials 0.000 claims description 2
- YQHLDYVWEZKEOX-UHFFFAOYSA-N cumene hydroperoxide Chemical compound OOC(C)(C)C1=CC=CC=C1 YQHLDYVWEZKEOX-UHFFFAOYSA-N 0.000 claims description 2
- 229910021485 fumed silica Inorganic materials 0.000 claims description 2
- 239000010453 quartz Substances 0.000 claims description 2
- 238000004806 packaging method and process Methods 0.000 claims 5
- 239000002904 solvent Substances 0.000 claims 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 3
- 150000007513 acids Chemical class 0.000 claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 2
- 239000005407 aluminoborosilicate glass Substances 0.000 claims 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- 239000004568 cement Substances 0.000 claims 2
- 229910044991 metal oxide Inorganic materials 0.000 claims 2
- 150000004706 metal oxides Chemical class 0.000 claims 2
- 150000004767 nitrides Chemical class 0.000 claims 2
- 150000003014 phosphoric acid esters Chemical class 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- AKUNSTOMHUXJOZ-UHFFFAOYSA-N 1-hydroperoxybutane Chemical compound CCCCOO AKUNSTOMHUXJOZ-UHFFFAOYSA-N 0.000 claims 1
- XRXANEMIFVRKLN-UHFFFAOYSA-N 2-hydroperoxy-2-methylbutane Chemical compound CCC(C)(C)OO XRXANEMIFVRKLN-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- MQSMIOKTOYAPHO-WEVVVXLNSA-N [(e)-5-hydroperoxypent-1-enyl]benzene Chemical compound OOCCC\C=C\C1=CC=CC=C1 MQSMIOKTOYAPHO-WEVVVXLNSA-N 0.000 claims 1
- 150000008065 acid anhydrides Chemical class 0.000 claims 1
- 239000005354 aluminosilicate glass Substances 0.000 claims 1
- 239000004327 boric acid Substances 0.000 claims 1
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims 1
- 239000008119 colloidal silica Substances 0.000 claims 1
- 238000005336 cracking Methods 0.000 claims 1
- 239000008393 encapsulating agent Substances 0.000 claims 1
- 229910052735 hafnium Inorganic materials 0.000 claims 1
- 239000010954 inorganic particle Substances 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical class 0.000 claims 1
- 229910052746 lanthanum Inorganic materials 0.000 claims 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims 1
- 239000013615 primer Substances 0.000 claims 1
- 239000002987 primer (paints) Substances 0.000 claims 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 1
- 239000000565 sealant Substances 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 230000003068 static effect Effects 0.000 claims 1
- 229910052712 strontium Inorganic materials 0.000 claims 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 claims 1
- 150000003455 sulfinic acids Chemical class 0.000 claims 1
- 150000003460 sulfonic acids Chemical class 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 229910052727 yttrium Inorganic materials 0.000 claims 1
- 229910052725 zinc Inorganic materials 0.000 claims 1
- 229910052726 zirconium Inorganic materials 0.000 claims 1
- 229910001928 zirconium oxide Inorganic materials 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 abstract description 8
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 66
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 36
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 9
- 229910052802 copper Inorganic materials 0.000 description 9
- 239000010949 copper Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 7
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 6
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 150000001879 copper Chemical class 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 5
- IPCRBOOJBPETMF-UHFFFAOYSA-N N-acetylthiourea Chemical compound CC(=O)NC(N)=S IPCRBOOJBPETMF-UHFFFAOYSA-N 0.000 description 5
- 238000002845 discoloration Methods 0.000 description 5
- 238000006479 redox reaction Methods 0.000 description 4
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 3
- KQJQICVXLJTWQD-UHFFFAOYSA-N N-Methylthiourea Chemical compound CNC(N)=S KQJQICVXLJTWQD-UHFFFAOYSA-N 0.000 description 3
- 235000019400 benzoyl peroxide Nutrition 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 150000002736 metal compounds Chemical class 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- HXCHZMHFZXNFIX-UHFFFAOYSA-N (2-methoxyphenyl)thiourea Chemical compound COC1=CC=CC=C1NC(N)=S HXCHZMHFZXNFIX-UHFFFAOYSA-N 0.000 description 2
- YKOBLHQALWQKTC-UHFFFAOYSA-N (3-fluorophenyl)thiourea Chemical compound NC(=S)NC1=CC=CC(F)=C1 YKOBLHQALWQKTC-UHFFFAOYSA-N 0.000 description 2
- YGMXDSWMRIXNTI-UHFFFAOYSA-N (3-methoxyphenyl)thiourea Chemical compound COC1=CC=CC(NC(N)=S)=C1 YGMXDSWMRIXNTI-UHFFFAOYSA-N 0.000 description 2
- QGLYTNIXHPCRCF-UHFFFAOYSA-N (4-ethoxyphenyl)thiourea Chemical compound CCOC1=CC=C(NC(N)=S)C=C1 QGLYTNIXHPCRCF-UHFFFAOYSA-N 0.000 description 2
- BRWKXKNZRVALNZ-UHFFFAOYSA-N (4-fluorophenyl)thiourea Chemical compound NC(=S)NC1=CC=C(F)C=C1 BRWKXKNZRVALNZ-UHFFFAOYSA-N 0.000 description 2
- SRYLJBWDZZMDSK-UHFFFAOYSA-N (4-methoxyphenyl)thiourea Chemical compound COC1=CC=C(NC(N)=S)C=C1 SRYLJBWDZZMDSK-UHFFFAOYSA-N 0.000 description 2
- PZCDNWLGSCLQCC-UHFFFAOYSA-N 1-(4-methoxyphenyl)-3-pyridin-2-ylthiourea Chemical compound C1=CC(OC)=CC=C1NC(=S)NC1=CC=CC=N1 PZCDNWLGSCLQCC-UHFFFAOYSA-N 0.000 description 2
- NXCBDDGSOXJEFZ-UHFFFAOYSA-N 1-benzyl-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NCC1=CC=CC=C1 NXCBDDGSOXJEFZ-UHFFFAOYSA-N 0.000 description 2
- KPHXIOWPVPBEKR-UHFFFAOYSA-N 1-phenyl-3-(1-phenylethyl)thiourea Chemical compound C=1C=CC=CC=1C(C)NC(=S)NC1=CC=CC=C1 KPHXIOWPVPBEKR-UHFFFAOYSA-N 0.000 description 2
- MQCPOLNSJCWPGT-UHFFFAOYSA-N 2,2'-Bisphenol F Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1O MQCPOLNSJCWPGT-UHFFFAOYSA-N 0.000 description 2
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
- JRQJYVACDJEUDZ-UHFFFAOYSA-N 3-(carbamothioylamino)benzoic acid Chemical compound NC(=S)NC1=CC=CC(C(O)=O)=C1 JRQJYVACDJEUDZ-UHFFFAOYSA-N 0.000 description 2
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- FCSHMCFRCYZTRQ-UHFFFAOYSA-N N,N'-diphenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1=CC=CC=C1 FCSHMCFRCYZTRQ-UHFFFAOYSA-N 0.000 description 2
- FULZLIGZKMKICU-UHFFFAOYSA-N N-phenylthiourea Chemical compound NC(=S)NC1=CC=CC=C1 FULZLIGZKMKICU-UHFFFAOYSA-N 0.000 description 2
- AMFGWXWBFGVCKG-UHFFFAOYSA-N Panavia opaque Chemical compound C1=CC(OCC(O)COC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OCC(O)COC(=O)C(C)=C)C=C1 AMFGWXWBFGVCKG-UHFFFAOYSA-N 0.000 description 2
- RIDAQLWHGMOKNW-UHFFFAOYSA-N [3-(carbamimidoylsulfanylmethyl)phenyl]methyl methanimidothioate Chemical compound C1=CC(=CC(=C1)CSC(=N)N)CSC=N RIDAQLWHGMOKNW-UHFFFAOYSA-N 0.000 description 2
- WKRUQAYFMKZMPJ-UHFFFAOYSA-N [3-(trifluoromethyl)phenyl]thiourea Chemical compound NC(=S)NC1=CC=CC(C(F)(F)F)=C1 WKRUQAYFMKZMPJ-UHFFFAOYSA-N 0.000 description 2
- VVAYUDFHMYSYOU-UHFFFAOYSA-N [4-(carbamimidoylsulfanylmethyl)phenyl]methyl methanimidothioate Chemical compound C1=CC(=CC=C1CSC=N)CSC(=N)N VVAYUDFHMYSYOU-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 150000007656 barbituric acids Chemical class 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- QUZSUMLPWDHKCJ-UHFFFAOYSA-N bisphenol A dimethacrylate Chemical compound C1=CC(OC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OC(=O)C(C)=C)C=C1 QUZSUMLPWDHKCJ-UHFFFAOYSA-N 0.000 description 2
- GMEGXJPUFRVCPX-UHFFFAOYSA-N butylthiourea Chemical compound CCCCNC(N)=S GMEGXJPUFRVCPX-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- YEOCHZFPBYUXMC-UHFFFAOYSA-L copper benzoate Chemical compound [Cu+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 YEOCHZFPBYUXMC-UHFFFAOYSA-L 0.000 description 2
- 229910001431 copper ion Inorganic materials 0.000 description 2
- 239000005548 dental material Substances 0.000 description 2
- MKVYSRNJLWTVIK-UHFFFAOYSA-N ethyl carbamate;2-methylprop-2-enoic acid Chemical compound CCOC(N)=O.CC(=C)C(O)=O.CC(=C)C(O)=O MKVYSRNJLWTVIK-UHFFFAOYSA-N 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- OYQJFWIXVCUZEO-UHFFFAOYSA-N hydrogen peroxide;thiourea Chemical compound OO.NC(N)=S OYQJFWIXVCUZEO-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- UJNPFRWNURYKFC-UHFFFAOYSA-N n-(dimethylcarbamothioyl)benzamide Chemical compound CN(C)C(=S)NC(=O)C1=CC=CC=C1 UJNPFRWNURYKFC-UHFFFAOYSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- XAYQUBJWNNEKCO-UHFFFAOYSA-N (1,1-dioxo-2,5-dihydrothiophen-3-yl)methyl carbamimidothioate Chemical compound NC(=N)SCC1=CCS(=O)(=O)C1 XAYQUBJWNNEKCO-UHFFFAOYSA-N 0.000 description 1
- HAXRIUKKDXWGLU-SGWCAAJKSA-N (1E)-1-[(4-hydroxy-6-methyl-2-oxopyran-3-yl)methylidene]-3-octadecylthiourea Chemical compound CCCCCCCCCCCCCCCCCCNC(=S)\N=C\c1c(O)cc(C)oc1=O HAXRIUKKDXWGLU-SGWCAAJKSA-N 0.000 description 1
- WWKSOQLEJQRSQH-OVCLIPMQSA-N (1E)-1-[(4-hydroxy-6-methyl-2-oxopyran-3-yl)methylidene]-3-phenylthiourea Chemical compound Cc1cc(O)c(\C=N\C(=S)Nc2ccccc2)c(=O)o1 WWKSOQLEJQRSQH-OVCLIPMQSA-N 0.000 description 1
- OUTYNBVXPUYWLB-RBKNKUFQSA-N (1E)-1-[(E)-2-benzoyl-3-hydroxy-3-phenylprop-2-enylidene]-3-(2-tert-butyl-6-ethylphenyl)thiourea Chemical compound CCc1cccc(c1NC(=S)\N=C\C(=C(/O)c1ccccc1)\C(=O)c1ccccc1)C(C)(C)C OUTYNBVXPUYWLB-RBKNKUFQSA-N 0.000 description 1
- UUQZTECZSCPOLX-UHFFFAOYSA-N (2,3-difluorophenyl)thiourea Chemical compound NC(=S)NC1=CC=CC(F)=C1F UUQZTECZSCPOLX-UHFFFAOYSA-N 0.000 description 1
- VDTKXIMDQWHJSA-UHFFFAOYSA-N (2,3-dimethylphenyl)thiourea Chemical compound CC1=CC=CC(NC(N)=S)=C1C VDTKXIMDQWHJSA-UHFFFAOYSA-N 0.000 description 1
- ACUIIYNEUHWWGT-UHFFFAOYSA-N (2,4,6-tribromophenyl)thiourea Chemical compound NC(=S)NC1=C(Br)C=C(Br)C=C1Br ACUIIYNEUHWWGT-UHFFFAOYSA-N 0.000 description 1
- ZUSZPZPGZMEXLA-UHFFFAOYSA-N (2,4,6-trichlorophenyl)thiourea Chemical compound NC(=S)NC1=C(Cl)C=C(Cl)C=C1Cl ZUSZPZPGZMEXLA-UHFFFAOYSA-N 0.000 description 1
- LBUGQLLKHAHCJJ-UHFFFAOYSA-N (2,4,6-trimethylphenyl)thiourea Chemical compound CC1=CC(C)=C(NC(N)=S)C(C)=C1 LBUGQLLKHAHCJJ-UHFFFAOYSA-N 0.000 description 1
- FVQQNJKFOMSMDF-UHFFFAOYSA-N (2,4,6-trioxo-1,3-diazinan-5-ylidene)methylthiourea Chemical compound NC(=S)NC=C1C(=O)NC(=O)NC1=O FVQQNJKFOMSMDF-UHFFFAOYSA-N 0.000 description 1
- HSWCDFOASWNGOM-UHFFFAOYSA-N (2,4-dichlorophenyl)thiourea Chemical compound NC(=S)NC1=CC=C(Cl)C=C1Cl HSWCDFOASWNGOM-UHFFFAOYSA-N 0.000 description 1
- DZZSKQFBAGZNSH-UHFFFAOYSA-N (2,4-difluorophenyl)thiourea Chemical compound NC(=S)NC1=CC=C(F)C=C1F DZZSKQFBAGZNSH-UHFFFAOYSA-N 0.000 description 1
- KAGLPYRXTCQWHU-UHFFFAOYSA-N (2,4-dimethylphenyl)thiourea Chemical compound CC1=CC=C(NC(N)=S)C(C)=C1 KAGLPYRXTCQWHU-UHFFFAOYSA-N 0.000 description 1
- UQCOANNCPUOZNW-UHFFFAOYSA-N (2,5-dichlorophenyl)thiourea Chemical compound NC(=S)NC1=CC(Cl)=CC=C1Cl UQCOANNCPUOZNW-UHFFFAOYSA-N 0.000 description 1
- JBWSNSWRTOFDBM-UHFFFAOYSA-N (2,5-difluorophenyl)thiourea Chemical compound NC(=S)NC1=CC(F)=CC=C1F JBWSNSWRTOFDBM-UHFFFAOYSA-N 0.000 description 1
- AWPKXPUZILRUDJ-UHFFFAOYSA-N (2,6-difluorophenyl)thiourea Chemical compound NC(=S)NC1=C(F)C=CC=C1F AWPKXPUZILRUDJ-UHFFFAOYSA-N 0.000 description 1
- ASNKJUONFPQYPC-UHFFFAOYSA-N (2,6-dimethylphenyl)thiourea Chemical compound CC1=CC=CC(C)=C1NC(S)=N ASNKJUONFPQYPC-UHFFFAOYSA-N 0.000 description 1
- QIGMVYSPXPXCPN-UHFFFAOYSA-N (2-bromophenyl)thiourea Chemical compound NC(=S)NC1=CC=CC=C1Br QIGMVYSPXPXCPN-UHFFFAOYSA-N 0.000 description 1
- MSVNRONZSZGDLW-UHFFFAOYSA-N (2-hexadecylsulfanylphenyl)thiourea Chemical compound CCCCCCCCCCCCCCCCSC1=CC=CC=C1NC(N)=S MSVNRONZSZGDLW-UHFFFAOYSA-N 0.000 description 1
- ZHVXETDHOROSGO-UHFFFAOYSA-N (3,4,5-trimethoxyphenyl)thiourea Chemical compound COC1=CC(NC(N)=S)=CC(OC)=C1OC ZHVXETDHOROSGO-UHFFFAOYSA-N 0.000 description 1
- CCNCITSJXCSXJY-UHFFFAOYSA-N (3,4-dichlorophenyl)thiourea Chemical compound NC(=S)NC1=CC=C(Cl)C(Cl)=C1 CCNCITSJXCSXJY-UHFFFAOYSA-N 0.000 description 1
- SVVAZPFKTDKAAN-UHFFFAOYSA-N (3,4-dimethylphenyl)thiourea Chemical compound CC1=CC=C(NC(N)=S)C=C1C SVVAZPFKTDKAAN-UHFFFAOYSA-N 0.000 description 1
- BNJARXOEVLYKDN-UHFFFAOYSA-N (3,5-dichlorophenyl)thiourea Chemical compound NC(=S)NC1=CC(Cl)=CC(Cl)=C1 BNJARXOEVLYKDN-UHFFFAOYSA-N 0.000 description 1
- LSYZRUOXXOTVAV-UHFFFAOYSA-N (3-chlorophenyl)thiourea Chemical compound NC(=S)NC1=CC=CC(Cl)=C1 LSYZRUOXXOTVAV-UHFFFAOYSA-N 0.000 description 1
- VNRXRPBDGKIBKS-UHFFFAOYSA-N (3-cyanophenyl)thiourea Chemical compound NC(=S)NC1=CC=CC(C#N)=C1 VNRXRPBDGKIBKS-UHFFFAOYSA-N 0.000 description 1
- BHJYKFUCQNISJA-UHFFFAOYSA-N (3-hydroxyphenyl)thiourea Chemical compound NC(=S)NC1=CC=CC(O)=C1 BHJYKFUCQNISJA-UHFFFAOYSA-N 0.000 description 1
- ZMKCWZXPSQTQHC-UHFFFAOYSA-N (3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)methylthiourea Chemical compound O=C1C(=CNC(N)=S)C(C)=NN1C1=CC=CC=C1 ZMKCWZXPSQTQHC-UHFFFAOYSA-N 0.000 description 1
- UGHBMZQASZAIAZ-RQZCQDPDSA-N (3E)-1-butyl-3-[(4-hydroxy-2-oxo-1H-quinolin-3-yl)methylidene]thiourea Chemical compound CCCCNC(=S)\N=C\c1c(O)c2ccccc2[nH]c1=O UGHBMZQASZAIAZ-RQZCQDPDSA-N 0.000 description 1
- XVEFWRUIYOXUGG-UHFFFAOYSA-N (4-chlorophenyl)thiourea Chemical compound NC(=S)NC1=CC=C(Cl)C=C1 XVEFWRUIYOXUGG-UHFFFAOYSA-N 0.000 description 1
- HCGOHCAOJSIHNG-UHFFFAOYSA-N (4-hexadecylsulfonylphenyl)thiourea Chemical compound CCCCCCCCCCCCCCCCS(=O)(=O)C1=CC=C(NC(N)=S)C=C1 HCGOHCAOJSIHNG-UHFFFAOYSA-N 0.000 description 1
- MHPCCRCGEMSBCK-UHFFFAOYSA-N (4-hydroxy-1,1-dioxothiolan-3-yl) carbamimidothioate Chemical compound NC(=N)SC1CS(=O)(=O)CC1O MHPCCRCGEMSBCK-UHFFFAOYSA-N 0.000 description 1
- QICKOOCQSYZYQB-UHFFFAOYSA-N (4-hydroxyphenyl)thiourea Chemical compound NC(=S)NC1=CC=C(O)C=C1 QICKOOCQSYZYQB-UHFFFAOYSA-N 0.000 description 1
- PRQADQBMIVASQR-UHFFFAOYSA-N (4-methyl-1,1-dioxo-2,3-dihydrothiophen-3-yl) carbamimidate Chemical compound CC1=CS(=O)(=O)CC1OC(=N)N PRQADQBMIVASQR-UHFFFAOYSA-N 0.000 description 1
- GPDULBOKROYYSF-UHFFFAOYSA-N (4-methyl-1,1-dioxo-2,5-dihydrothiophen-3-yl) carbamimidate Chemical compound CC1=C(CS(=O)(=O)C1)OC(=N)N GPDULBOKROYYSF-UHFFFAOYSA-N 0.000 description 1
- VXLFMCZPFIKKDZ-UHFFFAOYSA-N (4-methylphenyl)thiourea Chemical compound CC1=CC=C(NC(N)=S)C=C1 VXLFMCZPFIKKDZ-UHFFFAOYSA-N 0.000 description 1
- BLYAANPIHFKKMQ-UHFFFAOYSA-N (4-nitrophenyl)thiourea Chemical compound NC(=S)NC1=CC=C([N+]([O-])=O)C=C1 BLYAANPIHFKKMQ-UHFFFAOYSA-N 0.000 description 1
- CDQMIFDISMKPDE-UHFFFAOYSA-N (4-tert-butylphenyl)thiourea Chemical compound CC(C)(C)C1=CC=C(NC(N)=S)C=C1 CDQMIFDISMKPDE-UHFFFAOYSA-N 0.000 description 1
- SFUKEILTSKBHQJ-UHFFFAOYSA-N (4-thiophen-2-yl-1,3-thiazol-2-yl)thiourea Chemical compound S1C(NC(=S)N)=NC(C=2SC=CC=2)=C1 SFUKEILTSKBHQJ-UHFFFAOYSA-N 0.000 description 1
- NGODYGDCMXDGFI-VAWYXSNFSA-N (e)-n-(benzylcarbamothioyl)-3-phenylprop-2-enamide Chemical compound C=1C=CC=CC=1/C=C/C(=O)NC(=S)NCC1=CC=CC=C1 NGODYGDCMXDGFI-VAWYXSNFSA-N 0.000 description 1
- ZEIHZWKMWIFFLX-MDWZMJQESA-N (e)-n-[(4-ethoxyphenyl)carbamothioyl]-3-phenylprop-2-enamide Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC(=O)\C=C\C1=CC=CC=C1 ZEIHZWKMWIFFLX-MDWZMJQESA-N 0.000 description 1
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- OLTJYOMEFRRCKA-UHFFFAOYSA-N 1,1,3-triphenylthiourea Chemical compound C=1C=CC=CC=1N(C=1C=CC=CC=1)C(=S)NC1=CC=CC=C1 OLTJYOMEFRRCKA-UHFFFAOYSA-N 0.000 description 1
- MMJSFGUIOQZNSL-UHFFFAOYSA-N 1,1-bis(2-cyanoethyl)-3-hexylthiourea Chemical compound CCCCCCNC(=S)N(CCC#N)CCC#N MMJSFGUIOQZNSL-UHFFFAOYSA-N 0.000 description 1
- ZGDZNLKZTKGOCC-UHFFFAOYSA-N 1,1-bis(2-hydroxyethyl)-3-phenylthiourea Chemical compound OCCN(CCO)C(=S)NC1=CC=CC=C1 ZGDZNLKZTKGOCC-UHFFFAOYSA-N 0.000 description 1
- JZLRCXAGPTUZSL-UHFFFAOYSA-N 1,1-bis(2-methylpropyl)-3-phenylthiourea Chemical compound CC(C)CN(CC(C)C)C(=S)NC1=CC=CC=C1 JZLRCXAGPTUZSL-UHFFFAOYSA-N 0.000 description 1
- DALNRYKLXQFYLE-UHFFFAOYSA-N 1,1-dibutyl-3-phenylthiourea Chemical compound CCCCN(CCCC)C(=S)NC1=CC=CC=C1 DALNRYKLXQFYLE-UHFFFAOYSA-N 0.000 description 1
- XIBHMHZQNXDDJY-UHFFFAOYSA-N 1,1-diethyl-3-phenylthiourea Chemical compound CCN(CC)C(=S)NC1=CC=CC=C1 XIBHMHZQNXDDJY-UHFFFAOYSA-N 0.000 description 1
- CVEXTBNTGSXEQS-UHFFFAOYSA-N 1,1-dimethyl-3-(2-methylphenyl)thiourea Chemical compound CN(C)C(=S)NC1=CC=CC=C1C CVEXTBNTGSXEQS-UHFFFAOYSA-N 0.000 description 1
- NVFPKSLOJQQWMO-UHFFFAOYSA-N 1,1-dimethyl-3-(4-methylphenyl)thiourea Chemical compound CN(C)C(=S)NC1=CC=C(C)C=C1 NVFPKSLOJQQWMO-UHFFFAOYSA-N 0.000 description 1
- QWWCEYOPFDUQPY-UHFFFAOYSA-N 1,1-dimethyl-3-(n-methyl-c-phenylcarbonimidoyl)thiourea Chemical compound CN(C)C(=S)NC(=NC)C1=CC=CC=C1 QWWCEYOPFDUQPY-UHFFFAOYSA-N 0.000 description 1
- JUSFFZFOIIGLRP-UHFFFAOYSA-N 1,1-dimethyl-3-phenylthiourea Chemical compound CN(C)C(=S)NC1=CC=CC=C1 JUSFFZFOIIGLRP-UHFFFAOYSA-N 0.000 description 1
- RJTJZLBYKUDXRD-UHFFFAOYSA-N 1,3-bis(2-chlorophenyl)thiourea Chemical compound ClC1=CC=CC=C1NC(=S)NC1=CC=CC=C1Cl RJTJZLBYKUDXRD-UHFFFAOYSA-N 0.000 description 1
- ZBMLHTDWAFZBDE-UHFFFAOYSA-N 1,3-bis(2-fluorophenyl)thiourea Chemical compound FC1=CC=CC=C1NC(=S)NC1=CC=CC=C1F ZBMLHTDWAFZBDE-UHFFFAOYSA-N 0.000 description 1
- SLCJUVBRGGUTNS-UHFFFAOYSA-N 1,3-bis(2-methoxyphenyl)thiourea Chemical compound COC1=CC=CC=C1NC(=S)NC1=CC=CC=C1OC SLCJUVBRGGUTNS-UHFFFAOYSA-N 0.000 description 1
- QRWSNTGGHGUSLK-UHFFFAOYSA-N 1,3-bis(3-acetylphenyl)thiourea Chemical compound CC(=O)C1=CC=CC(NC(=S)NC=2C=C(C=CC=2)C(C)=O)=C1 QRWSNTGGHGUSLK-UHFFFAOYSA-N 0.000 description 1
- QIUPJABVMBKYJD-UHFFFAOYSA-N 1,3-bis(3-bromophenyl)thiourea Chemical compound BrC1=CC=CC(NC(=S)NC=2C=C(Br)C=CC=2)=C1 QIUPJABVMBKYJD-UHFFFAOYSA-N 0.000 description 1
- CPSMRPMAUVPTLM-UHFFFAOYSA-N 1,3-bis(3-cyanophenyl)thiourea Chemical compound C=1C=CC(C#N)=CC=1NC(=S)NC1=CC=CC(C#N)=C1 CPSMRPMAUVPTLM-UHFFFAOYSA-N 0.000 description 1
- OCDRQBACVLHIFA-UHFFFAOYSA-N 1,3-bis(3-iodophenyl)thiourea Chemical compound IC1=CC=CC(NC(=S)NC=2C=C(I)C=CC=2)=C1 OCDRQBACVLHIFA-UHFFFAOYSA-N 0.000 description 1
- QEAYQEGWKKNUSF-UHFFFAOYSA-N 1,3-bis(3-methoxyphenyl)thiourea Chemical compound COC1=CC=CC(NC(=S)NC=2C=C(OC)C=CC=2)=C1 QEAYQEGWKKNUSF-UHFFFAOYSA-N 0.000 description 1
- QYXZLVQATVFGJH-UHFFFAOYSA-N 1,3-bis(3-nitrophenyl)thiourea Chemical compound [O-][N+](=O)C1=CC=CC(NC(=S)NC=2C=C(C=CC=2)[N+]([O-])=O)=C1 QYXZLVQATVFGJH-UHFFFAOYSA-N 0.000 description 1
- RQVXFYAPGIMASB-UHFFFAOYSA-N 1,3-bis(4-bromophenyl)thiourea Chemical compound C1=CC(Br)=CC=C1NC(=S)NC1=CC=C(Br)C=C1 RQVXFYAPGIMASB-UHFFFAOYSA-N 0.000 description 1
- SYJZYFOTCABQES-UHFFFAOYSA-N 1,3-bis(4-chlorophenyl)thiourea Chemical compound C1=CC(Cl)=CC=C1NC(=S)NC1=CC=C(Cl)C=C1 SYJZYFOTCABQES-UHFFFAOYSA-N 0.000 description 1
- PRXHANOJNVGVGC-UHFFFAOYSA-N 1,3-bis(4-ethoxyphenyl)thiourea Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC1=CC=C(OCC)C=C1 PRXHANOJNVGVGC-UHFFFAOYSA-N 0.000 description 1
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- DZZWKUMHMSNBSG-UHFFFAOYSA-N 1,3-bis(prop-2-enyl)thiourea Chemical compound C=CCNC(=S)NCC=C DZZWKUMHMSNBSG-UHFFFAOYSA-N 0.000 description 1
- KWZKQWNJGMWSDK-UHFFFAOYSA-N 1,3-bis(pyridin-3-ylmethyl)thiourea Chemical compound C=1C=CN=CC=1CNC(=S)NCC1=CC=CN=C1 KWZKQWNJGMWSDK-UHFFFAOYSA-N 0.000 description 1
- KREOCUNMMFZOOS-UHFFFAOYSA-N 1,3-di(propan-2-yl)thiourea Chemical compound CC(C)NC(S)=NC(C)C KREOCUNMMFZOOS-UHFFFAOYSA-N 0.000 description 1
- HWTXGJSULITOJM-UHFFFAOYSA-N 1,3-di(tetradecyl)thiourea Chemical compound CCCCCCCCCCCCCCNC(=S)NCCCCCCCCCCCCCC HWTXGJSULITOJM-UHFFFAOYSA-N 0.000 description 1
- LQZPSWMMTICWHD-UHFFFAOYSA-N 1,3-dibenzylthiourea Chemical compound C=1C=CC=CC=1CNC(=S)NCC1=CC=CC=C1 LQZPSWMMTICWHD-UHFFFAOYSA-N 0.000 description 1
- KAJICSGLHKRDLN-UHFFFAOYSA-N 1,3-dicyclohexylthiourea Chemical compound C1CCCCC1NC(=S)NC1CCCCC1 KAJICSGLHKRDLN-UHFFFAOYSA-N 0.000 description 1
- KVPJJDWEFYTGMD-UHFFFAOYSA-N 1,3-didecylthiourea Chemical compound CCCCCCCCCCNC(=S)NCCCCCCCCCC KVPJJDWEFYTGMD-UHFFFAOYSA-N 0.000 description 1
- NWFVONWTBGQHGT-UHFFFAOYSA-N 1,3-didodecylthiourea Chemical compound CCCCCCCCCCCCNC(=S)NCCCCCCCCCCCC NWFVONWTBGQHGT-UHFFFAOYSA-N 0.000 description 1
- ZVFTWKBRNQSRLB-UHFFFAOYSA-N 1,3-diheptylthiourea Chemical compound CCCCCCCNC(=S)NCCCCCCC ZVFTWKBRNQSRLB-UHFFFAOYSA-N 0.000 description 1
- AMZQAMADELMUOH-UHFFFAOYSA-N 1,3-dihexadecylthiourea Chemical compound CCCCCCCCCCCCCCCCNC(=S)NCCCCCCCCCCCCCCCC AMZQAMADELMUOH-UHFFFAOYSA-N 0.000 description 1
- CYYJFWJNIQDCLT-UHFFFAOYSA-N 1,3-dihexylthiourea Chemical compound CCCCCCNC(=S)NCCCCCC CYYJFWJNIQDCLT-UHFFFAOYSA-N 0.000 description 1
- RNGRBOULPSEYNL-UHFFFAOYSA-N 1,3-dioctylthiourea Chemical compound CCCCCCCCNC(=S)NCCCCCCCC RNGRBOULPSEYNL-UHFFFAOYSA-N 0.000 description 1
- AUXGIIVHLRLBSG-UHFFFAOYSA-N 1,3-dipropylthiourea Chemical compound CCCNC(=S)NCCC AUXGIIVHLRLBSG-UHFFFAOYSA-N 0.000 description 1
- LTMHEXFMSAISLN-UHFFFAOYSA-N 1,3-ditert-butylthiourea Chemical compound CC(C)(C)NC(=S)NC(C)(C)C LTMHEXFMSAISLN-UHFFFAOYSA-N 0.000 description 1
- ATOUXIOKEJWULN-UHFFFAOYSA-N 1,6-diisocyanato-2,2,4-trimethylhexane Chemical compound O=C=NCCC(C)CC(C)(C)CN=C=O ATOUXIOKEJWULN-UHFFFAOYSA-N 0.000 description 1
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 1
- BTWZTAVBIVNLDT-UHFFFAOYSA-N 1-(1,1-dioxothiolan-3-yl)-1-methyl-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)N(C)C1CCS(=O)(=O)C1 BTWZTAVBIVNLDT-UHFFFAOYSA-N 0.000 description 1
- VXMNLNPMEWKCMJ-UHFFFAOYSA-N 1-(1,2-diphenylethyl)-3-(2-methylphenyl)thiourea Chemical compound CC1=CC=CC=C1NC(=S)NC(C=1C=CC=CC=1)CC1=CC=CC=C1 VXMNLNPMEWKCMJ-UHFFFAOYSA-N 0.000 description 1
- DTTHRUFYGCMDQT-UHFFFAOYSA-N 1-(1,2-diphenylethyl)-3-(4-ethoxyphenyl)thiourea Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC(C=1C=CC=CC=1)CC1=CC=CC=C1 DTTHRUFYGCMDQT-UHFFFAOYSA-N 0.000 description 1
- UCIYYZVCWTXJKJ-UHFFFAOYSA-N 1-(1,2-diphenylethyl)-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC(C=1C=CC=CC=1)CC1=CC=CC=C1 UCIYYZVCWTXJKJ-UHFFFAOYSA-N 0.000 description 1
- CBUSXNYHLMPPND-UHFFFAOYSA-N 1-(1,3-benzothiazol-2-yl)-3-phenylthiourea Chemical compound N=1C2=CC=CC=C2SC=1NC(=S)NC1=CC=CC=C1 CBUSXNYHLMPPND-UHFFFAOYSA-N 0.000 description 1
- YGXLLLUEADCXET-UHFFFAOYSA-N 1-(1,5-dimethyl-3-oxo-2-phenylpyrazol-4-yl)-3-phenylthiourea Chemical compound O=C1N(C=2C=CC=CC=2)N(C)C(C)=C1NC(=S)NC1=CC=CC=C1 YGXLLLUEADCXET-UHFFFAOYSA-N 0.000 description 1
- WDGSTMYQKKBSCO-UHFFFAOYSA-N 1-(1-ethylpiperidin-3-yl)-3-phenylthiourea Chemical compound C1N(CC)CCCC1NC(=S)NC1=CC=CC=C1 WDGSTMYQKKBSCO-UHFFFAOYSA-N 0.000 description 1
- WZESFECOWWNXME-UHFFFAOYSA-N 1-(1-phenylethyl)-3-(pyridin-4-ylmethyl)thiourea Chemical compound C=1C=CC=CC=1C(C)NC(=S)NCC1=CC=NC=C1 WZESFECOWWNXME-UHFFFAOYSA-N 0.000 description 1
- IURJZJRJXQSLRJ-UHFFFAOYSA-N 1-(2,2-dimethylpropyl)-3-(2-fluorophenyl)thiourea Chemical compound CC(C)(C)CNC(=S)NC1=CC=CC=C1F IURJZJRJXQSLRJ-UHFFFAOYSA-N 0.000 description 1
- LABCXHGCVMRMIQ-UHFFFAOYSA-N 1-(2,4-difluorophenyl)-3-(2-fluorophenyl)thiourea Chemical compound FC1=CC(F)=CC=C1NC(=S)NC1=CC=CC=C1F LABCXHGCVMRMIQ-UHFFFAOYSA-N 0.000 description 1
- KIQKEDDXPCRXDY-UHFFFAOYSA-N 1-(2,4-difluorophenyl)-3-(4-phenoxyphenyl)thiourea Chemical compound FC1=CC(F)=CC=C1NC(=S)NC(C=C1)=CC=C1OC1=CC=CC=C1 KIQKEDDXPCRXDY-UHFFFAOYSA-N 0.000 description 1
- VWETUTNWDJXAMP-UHFFFAOYSA-N 1-(2,4-difluorophenyl)-3-ethylthiourea Chemical compound CCNC(=S)NC1=CC=C(F)C=C1F VWETUTNWDJXAMP-UHFFFAOYSA-N 0.000 description 1
- XLIOLSGWQDRJFC-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)-3-(1,2-diphenylethyl)thiourea Chemical compound CC1=CC(C)=CC=C1NC(=S)NC(C=1C=CC=CC=1)CC1=CC=CC=C1 XLIOLSGWQDRJFC-UHFFFAOYSA-N 0.000 description 1
- PRXUWVKXOYGADQ-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)-3-(2-hydroxyethyl)thiourea Chemical compound CC1=CC=C(NC(=S)NCCO)C(C)=C1 PRXUWVKXOYGADQ-UHFFFAOYSA-N 0.000 description 1
- TWOSLMVCMRLBKT-UHFFFAOYSA-N 1-(2,5-dichlorophenyl)-3-phenylthiourea Chemical compound ClC1=CC=C(Cl)C(NC(=S)NC=2C=CC=CC=2)=C1 TWOSLMVCMRLBKT-UHFFFAOYSA-N 0.000 description 1
- JVBGNPPYXIWVPH-UHFFFAOYSA-N 1-(2,5-dimethoxyphenyl)-3-methylthiourea Chemical compound CNC(=S)NC1=CC(OC)=CC=C1OC JVBGNPPYXIWVPH-UHFFFAOYSA-N 0.000 description 1
- DYIPNXQBWVUFEX-UHFFFAOYSA-N 1-(2,5-dimethoxyphenyl)-3-phenylthiourea Chemical compound COC1=CC=C(OC)C(NC(=S)NC=2C=CC=CC=2)=C1 DYIPNXQBWVUFEX-UHFFFAOYSA-N 0.000 description 1
- CIHQGCMTNXGTCT-UHFFFAOYSA-N 1-(2,5-dimethoxyphenyl)-3-propylthiourea Chemical compound CCCNC(=S)NC1=CC(OC)=CC=C1OC CIHQGCMTNXGTCT-UHFFFAOYSA-N 0.000 description 1
- FJXIXOZQHWBPIM-UHFFFAOYSA-N 1-(2,5-dimethylmorpholin-4-yl)-3-phenylthiourea Chemical compound CC1COC(C)CN1NC(=S)NC1=CC=CC=C1 FJXIXOZQHWBPIM-UHFFFAOYSA-N 0.000 description 1
- UMHKCUVTOFKSSQ-UHFFFAOYSA-N 1-(2,6-diethylphenyl)-3-(4-hydroxyphenyl)thiourea Chemical compound CCC1=CC=CC(CC)=C1NC(=S)NC1=CC=C(O)C=C1 UMHKCUVTOFKSSQ-UHFFFAOYSA-N 0.000 description 1
- OQPVXPIWXQMCJK-UHFFFAOYSA-N 1-(2,6-dimethylphenyl)-3-(pyridin-4-ylmethyl)thiourea Chemical compound CC1=CC=CC(C)=C1NC(=S)NCC1=CC=NC=C1 OQPVXPIWXQMCJK-UHFFFAOYSA-N 0.000 description 1
- TUBKWJOKKMOSFH-UHFFFAOYSA-N 1-(2,6-dimethylphenyl)-3-methylthiourea Chemical compound CNC(=S)NC1=C(C)C=CC=C1C TUBKWJOKKMOSFH-UHFFFAOYSA-N 0.000 description 1
- FXEJNAAFZARADY-UHFFFAOYSA-N 1-(2,6-dimethylphenyl)-3-phenylthiourea Chemical compound CC1=CC=CC(C)=C1NC(=S)NC1=CC=CC=C1 FXEJNAAFZARADY-UHFFFAOYSA-N 0.000 description 1
- FAQVSTDZNOROOV-UHFFFAOYSA-N 1-(2-benzylsulfinyl-2-phenylethenyl)-3-(2-tert-butyl-6-ethylphenyl)thiourea Chemical compound CCC1=CC=CC(C(C)(C)C)=C1NC(=S)NC=C(S(=O)CC=1C=CC=CC=1)C1=CC=CC=C1 FAQVSTDZNOROOV-UHFFFAOYSA-N 0.000 description 1
- ISKROPZRMFFRSM-UHFFFAOYSA-N 1-(2-bromo-4-methylphenyl)-3-phenylthiourea Chemical compound BrC1=CC(C)=CC=C1NC(=S)NC1=CC=CC=C1 ISKROPZRMFFRSM-UHFFFAOYSA-N 0.000 description 1
- UGGWKBPHDGYZTE-UHFFFAOYSA-N 1-(2-chloro-4-nitrophenyl)-3-ethylthiourea Chemical compound CCNC(=S)NC1=CC=C([N+]([O-])=O)C=C1Cl UGGWKBPHDGYZTE-UHFFFAOYSA-N 0.000 description 1
- GJXBIVMCTDXUKR-UHFFFAOYSA-N 1-(2-chlorophenyl)-3-phenylthiourea Chemical compound ClC1=CC=CC=C1NC(=S)NC1=CC=CC=C1 GJXBIVMCTDXUKR-UHFFFAOYSA-N 0.000 description 1
- FHBRDAGWNMJITB-UHFFFAOYSA-N 1-(2-ethoxyphenyl)-3-prop-2-enylthiourea Chemical compound CCOC1=CC=CC=C1NC(=S)NCC=C FHBRDAGWNMJITB-UHFFFAOYSA-N 0.000 description 1
- KNFHIVURXPEXMC-UHFFFAOYSA-N 1-(2-ethylphenyl)-3-methylthiourea Chemical compound CCC1=CC=CC=C1NC(=S)NC KNFHIVURXPEXMC-UHFFFAOYSA-N 0.000 description 1
- HCEZOXQABNTWFL-UHFFFAOYSA-N 1-(2-hydroxy-1-phenylethyl)-3-phenylthiourea Chemical compound C=1C=CC=CC=1C(CO)NC(=S)NC1=CC=CC=C1 HCEZOXQABNTWFL-UHFFFAOYSA-N 0.000 description 1
- LRJPRRZKTBEQCA-UHFFFAOYSA-N 1-(2-hydroxycyclohexyl)-3-phenylthiourea Chemical compound OC1CCCCC1NC(=S)NC1=CC=CC=C1 LRJPRRZKTBEQCA-UHFFFAOYSA-N 0.000 description 1
- MFCXZZJQPDIXAS-UHFFFAOYSA-N 1-(2-hydroxyethyl)-3-phenylthiourea Chemical compound OCCNC(=S)NC1=CC=CC=C1 MFCXZZJQPDIXAS-UHFFFAOYSA-N 0.000 description 1
- IZOQQRSXFDZTSD-UHFFFAOYSA-N 1-(2-methoxy-5-methylphenyl)-1-methyl-3-naphthalen-2-ylthiourea Chemical compound COC1=CC=C(C)C=C1N(C)C(=S)NC1=CC=C(C=CC=C2)C2=C1 IZOQQRSXFDZTSD-UHFFFAOYSA-N 0.000 description 1
- KVJVKEMWXRBCTP-UHFFFAOYSA-N 1-(2-methyl-2-morpholin-4-ylpropyl)-3-phenylthiourea Chemical compound C1COCCN1C(C)(C)CNC(=S)NC1=CC=CC=C1 KVJVKEMWXRBCTP-UHFFFAOYSA-N 0.000 description 1
- YRWMMPAJXUEPQM-UHFFFAOYSA-N 1-(2-methylphenyl)-3-(3-methyl-5-sulfanylidene-1h-1,2,4-triazol-4-yl)thiourea Chemical compound CC1=NNC(=S)N1NC(=S)NC1=CC=CC=C1C YRWMMPAJXUEPQM-UHFFFAOYSA-N 0.000 description 1
- BTAFYYYDRHFFDV-UHFFFAOYSA-N 1-(2-methylphenyl)-3-prop-2-enylthiourea Chemical compound CC1=CC=CC=C1NC(=S)NCC=C BTAFYYYDRHFFDV-UHFFFAOYSA-N 0.000 description 1
- NWZAUKPEJKZNCA-UHFFFAOYSA-N 1-(2-methylphenyl)-3-pyridin-2-ylthiourea Chemical compound CC1=CC=CC=C1NC(=S)NC1=CC=CC=N1 NWZAUKPEJKZNCA-UHFFFAOYSA-N 0.000 description 1
- HSOOIVBINKDISP-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(CCC)OC(=O)C(C)=C HSOOIVBINKDISP-UHFFFAOYSA-N 0.000 description 1
- FWTGTVWNYRCZAI-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCC(OC(=O)C(C)=C)OC(=O)C(C)=C FWTGTVWNYRCZAI-UHFFFAOYSA-N 0.000 description 1
- KQMPMWGWJLNKPC-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCC(OC(=O)C(C)=C)OC(=O)C(C)=C KQMPMWGWJLNKPC-UHFFFAOYSA-N 0.000 description 1
- VXYNGTDHEOPUHD-UHFFFAOYSA-N 1-(2-methylprop-2-enyl)-3-[6-(2-methylprop-2-enylcarbamothioylamino)pyridin-2-yl]thiourea Chemical compound CC(=C)CNC(=S)NC1=CC=CC(NC(=S)NCC(C)=C)=N1 VXYNGTDHEOPUHD-UHFFFAOYSA-N 0.000 description 1
- GYLIWROUPTWSLA-UHFFFAOYSA-N 1-(2-methylpropyl)-3-phenylthiourea Chemical compound CC(C)CNC(=S)NC1=CC=CC=C1 GYLIWROUPTWSLA-UHFFFAOYSA-N 0.000 description 1
- YNLDZXYYXGYXNA-UHFFFAOYSA-N 1-(2-nitrophenyl)-3-phenylthiourea Chemical compound [O-][N+](=O)C1=CC=CC=C1NC(=S)NC1=CC=CC=C1 YNLDZXYYXGYXNA-UHFFFAOYSA-N 0.000 description 1
- WDOSJUOKMFKKIP-UHFFFAOYSA-N 1-(3,3-dimethylbutan-2-yl)-3-[3-(trifluoromethyl)phenyl]thiourea Chemical compound CC(C)(C)C(C)NC(=S)NC1=CC=CC(C(F)(F)F)=C1 WDOSJUOKMFKKIP-UHFFFAOYSA-N 0.000 description 1
- HTPBJOMKIMAFQA-UHFFFAOYSA-N 1-(3,3-dimethylbutan-2-yl)-3-[4-(trifluoromethoxy)phenyl]thiourea Chemical compound CC(C)(C)C(C)NC(=S)NC1=CC=C(OC(F)(F)F)C=C1 HTPBJOMKIMAFQA-UHFFFAOYSA-N 0.000 description 1
- OEVOZUAJLIJWHI-UHFFFAOYSA-N 1-(3,3-dimethylbutan-2-yl)-3-[4-(trifluoromethylsulfanyl)phenyl]thiourea Chemical compound CC(C)(C)C(C)NC(=S)NC1=CC=C(SC(F)(F)F)C=C1 OEVOZUAJLIJWHI-UHFFFAOYSA-N 0.000 description 1
- QMIWMLSTKCUDPM-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-3-(4-sulfamoylphenyl)thiourea Chemical compound C1=CC(S(=O)(=O)N)=CC=C1NC(=S)NC1=CC=C(Cl)C(Cl)=C1 QMIWMLSTKCUDPM-UHFFFAOYSA-N 0.000 description 1
- QJAYUNBHNKSXFD-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-3-phenylthiourea Chemical compound C1=C(Cl)C(Cl)=CC=C1NC(=S)NC1=CC=CC=C1 QJAYUNBHNKSXFD-UHFFFAOYSA-N 0.000 description 1
- XGQJXGHFHUTGMU-UHFFFAOYSA-N 1-(3,4-dihydro-2h-pyrrol-5-yl)-1-phenylthiourea Chemical compound C=1C=CC=CC=1N(C(=S)N)C1=NCCC1 XGQJXGHFHUTGMU-UHFFFAOYSA-N 0.000 description 1
- SMDWBSIOSQLAMA-UHFFFAOYSA-N 1-(3,4-dimethylphenyl)-3-(2-pyridinyl)thiourea Chemical compound C1=C(C)C(C)=CC=C1NC(=S)NC1=CC=CC=N1 SMDWBSIOSQLAMA-UHFFFAOYSA-N 0.000 description 1
- HVFFCAJQMQNRGK-UHFFFAOYSA-N 1-(3,4-dimethylphenyl)-3-ethylthiourea Chemical compound CCNC(=S)NC1=CC=C(C)C(C)=C1 HVFFCAJQMQNRGK-UHFFFAOYSA-N 0.000 description 1
- WRHAGJCMAVKAIL-UHFFFAOYSA-N 1-(3-acetylphenyl)-3-prop-2-enylthiourea Chemical compound CC(=O)C1=CC=CC(NC(=S)NCC=C)=C1 WRHAGJCMAVKAIL-UHFFFAOYSA-N 0.000 description 1
- ULTRWDLJWYIHBR-UHFFFAOYSA-N 1-(3-butoxypropyl)-3-phenylthiourea Chemical compound CCCCOCCCNC(=S)NC1=CC=CC=C1 ULTRWDLJWYIHBR-UHFFFAOYSA-N 0.000 description 1
- YRBVLVKDMVTDDO-UHFFFAOYSA-N 1-(3-chlorophenyl)-3-phenylthiourea Chemical compound ClC1=CC=CC(NC(=S)NC=2C=CC=CC=2)=C1 YRBVLVKDMVTDDO-UHFFFAOYSA-N 0.000 description 1
- KBGFPBJKGWAOJR-UHFFFAOYSA-N 1-(3-fluorophenyl)-3-methylthiourea Chemical compound CNC(=S)NC1=CC=CC(F)=C1 KBGFPBJKGWAOJR-UHFFFAOYSA-N 0.000 description 1
- VCBKEHOPYOVCOQ-UHFFFAOYSA-N 1-(3-hydroxyphenyl)-3-(4-hydroxyphenyl)thiourea Chemical compound Oc1ccc(NC(=S)Nc2cccc(O)c2)cc1 VCBKEHOPYOVCOQ-UHFFFAOYSA-N 0.000 description 1
- BTFREYNHBKXMCJ-UHFFFAOYSA-N 1-(3-hydroxyphenyl)-3-phenylthiourea Chemical compound OC1=CC=CC(NC(=S)NC=2C=CC=CC=2)=C1 BTFREYNHBKXMCJ-UHFFFAOYSA-N 0.000 description 1
- JFDKTAJIUVDOGQ-UHFFFAOYSA-N 1-(3-methyl-5-sulfanylidene-1h-1,2,4-triazol-4-yl)-3-phenylthiourea Chemical compound CC1=NNC(=S)N1NC(=S)NC1=CC=CC=C1 JFDKTAJIUVDOGQ-UHFFFAOYSA-N 0.000 description 1
- SOGZSFQZVFEHOQ-UHFFFAOYSA-N 1-(3-methylphenyl)-3-(3-methyl-5-sulfanylidene-1h-1,2,4-triazol-4-yl)thiourea Chemical compound CC1=NNC(=S)N1NC(=S)NC1=CC=CC(C)=C1 SOGZSFQZVFEHOQ-UHFFFAOYSA-N 0.000 description 1
- WBVXPQGODRXOME-UHFFFAOYSA-N 1-(3-methylphenyl)-3-(4-methylpiperazin-1-yl)thiourea Chemical compound C1CN(C)CCN1NC(=S)NC1=CC=CC(C)=C1 WBVXPQGODRXOME-UHFFFAOYSA-N 0.000 description 1
- NVMXWDIGHPOMQP-UHFFFAOYSA-N 1-(3-nitrophenyl)-3-phenylthiourea Chemical compound [O-][N+](=O)C1=CC=CC(NC(=S)NC=2C=CC=CC=2)=C1 NVMXWDIGHPOMQP-UHFFFAOYSA-N 0.000 description 1
- OFUYWEOKKLWWNB-UHFFFAOYSA-N 1-(4-acetylphenyl)-3-methylthiourea Chemical compound CNC(=S)NC1=CC=C(C(C)=O)C=C1 OFUYWEOKKLWWNB-UHFFFAOYSA-N 0.000 description 1
- VCPIWOMTLPWHFX-UHFFFAOYSA-N 1-(4-bromophenyl)-3-(diaminomethylidene)thiourea Chemical compound NC(N)=NC(=S)NC1=CC=C(Br)C=C1 VCPIWOMTLPWHFX-UHFFFAOYSA-N 0.000 description 1
- ZLGSAJXFSIFRFC-UHFFFAOYSA-N 1-(4-chloro-2,5-dimethoxyphenyl)-3-(4-nitrophenyl)thiourea Chemical compound C1=C(Cl)C(OC)=CC(NC(=S)NC=2C=CC(=CC=2)[N+]([O-])=O)=C1OC ZLGSAJXFSIFRFC-UHFFFAOYSA-N 0.000 description 1
- LYCUOSUOUWKROB-UHFFFAOYSA-N 1-(4-chloro-2,5-dimethoxyphenyl)-3-methylthiourea Chemical compound CNC(=S)NC1=CC(OC)=C(Cl)C=C1OC LYCUOSUOUWKROB-UHFFFAOYSA-N 0.000 description 1
- HZVNREMABNFFPU-UHFFFAOYSA-N 1-(4-chloro-7-methoxyquinolin-2-yl)-3-phenylthiourea Chemical compound N=1C2=CC(OC)=CC=C2C(Cl)=CC=1NC(=S)NC1=CC=CC=C1 HZVNREMABNFFPU-UHFFFAOYSA-N 0.000 description 1
- ZQKZORJTEQWTQC-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-[5-(diethylamino)-2-methylphenyl]thiourea Chemical compound CCN(CC)C1=CC=C(C)C(NC(=S)NC=2C=CC(Cl)=CC=2)=C1 ZQKZORJTEQWTQC-UHFFFAOYSA-N 0.000 description 1
- XYAKDKSYCSTBMN-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-phenylthiourea Chemical compound C1=CC(Cl)=CC=C1NC(=S)NC1=CC=CC=C1 XYAKDKSYCSTBMN-UHFFFAOYSA-N 0.000 description 1
- NQGQESLZYNUKTB-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-pyridin-2-ylthiourea Chemical compound C1=CC(Cl)=CC=C1NC(=S)NC1=CC=CC=N1 NQGQESLZYNUKTB-UHFFFAOYSA-N 0.000 description 1
- YDYARPPTJXILQI-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-3-(4-methylpiperazin-1-yl)thiourea Chemical compound C1=CC(OCC)=CC=C1NC(=S)NN1CCN(C)CC1 YDYARPPTJXILQI-UHFFFAOYSA-N 0.000 description 1
- IZIKORVGYQJQMK-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-3-ethylthiourea Chemical compound CCNC(=S)NC1=CC=C(OCC)C=C1 IZIKORVGYQJQMK-UHFFFAOYSA-N 0.000 description 1
- MSYXWXRWGGQMFQ-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-3-pyridin-2-ylthiourea Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC1=CC=CC=N1 MSYXWXRWGGQMFQ-UHFFFAOYSA-N 0.000 description 1
- FHWFHUXCOGYFHS-UHFFFAOYSA-N 1-(4-ethylphenyl)-3-phenylthiourea Chemical compound C1=CC(CC)=CC=C1NC(=S)NC1=CC=CC=C1 FHWFHUXCOGYFHS-UHFFFAOYSA-N 0.000 description 1
- HHTITUNBJJLSLQ-UHFFFAOYSA-N 1-(4-fluorophenyl)-3-(2,4,6-trimethylphenyl)thiourea Chemical compound CC1=CC(C)=CC(C)=C1NC(=S)NC1=CC=C(F)C=C1 HHTITUNBJJLSLQ-UHFFFAOYSA-N 0.000 description 1
- NQEHXPPWIZNOQF-UHFFFAOYSA-N 1-(4-hydroxyphenyl)-3-propylthiourea Chemical compound CCCNC(=S)NC1=CC=C(O)C=C1 NQEHXPPWIZNOQF-UHFFFAOYSA-N 0.000 description 1
- JMKRMQGOPWYOGL-UHFFFAOYSA-N 1-(4-methoxyphenyl)-3-phenylthiourea Chemical compound C1=CC(OC)=CC=C1NC(=S)NC1=CC=CC=C1 JMKRMQGOPWYOGL-UHFFFAOYSA-N 0.000 description 1
- YJEJZZVROHEXFI-UHFFFAOYSA-N 1-(4-methyl-3-nitrophenyl)-3-propan-2-ylthiourea Chemical compound CC(C)NC(=S)NC1=CC=C(C)C([N+]([O-])=O)=C1 YJEJZZVROHEXFI-UHFFFAOYSA-N 0.000 description 1
- SCXFWPXUCRXSMM-UHFFFAOYSA-N 1-(4-methylphenyl)-3-(3-methyl-5-sulfanylidene-1h-1,2,4-triazol-4-yl)thiourea Chemical compound CC1=NNC(=S)N1NC(=S)NC1=CC=C(C)C=C1 SCXFWPXUCRXSMM-UHFFFAOYSA-N 0.000 description 1
- NZPBFKQKPZEPED-UHFFFAOYSA-N 1-(4-methylphenyl)-3-phenylthiourea Chemical compound C1=CC(C)=CC=C1NC(=S)NC1=CC=CC=C1 NZPBFKQKPZEPED-UHFFFAOYSA-N 0.000 description 1
- YRWXBKFHKPTRKR-UHFFFAOYSA-N 1-(4-methylphenyl)sulfonyl-3-phenylthiourea Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=S)NC1=CC=CC=C1 YRWXBKFHKPTRKR-UHFFFAOYSA-N 0.000 description 1
- OELRBZSULAMPKZ-UHFFFAOYSA-N 1-(4-nitrophenyl)-3-[3-(trifluoromethyl)phenyl]thiourea Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC(=S)NC1=CC=CC(C(F)(F)F)=C1 OELRBZSULAMPKZ-UHFFFAOYSA-N 0.000 description 1
- NNWRRGBHDKYELI-UHFFFAOYSA-N 1-(4-nitrophenyl)-3-phenylthiourea Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC(=S)NC1=CC=CC=C1 NNWRRGBHDKYELI-UHFFFAOYSA-N 0.000 description 1
- YCOCWYBOCCNPEX-UHFFFAOYSA-N 1-(5-anilino-1,2,4-thiadiazol-3-yl)-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC(N=1)=NSC=1NC1=CC=CC=C1 YCOCWYBOCCNPEX-UHFFFAOYSA-N 0.000 description 1
- QCWAEKJCJNGXQY-UHFFFAOYSA-N 1-(5-chloro-2,4-dimethoxyphenyl)-3-(2,5-difluorophenyl)thiourea Chemical compound COC1=CC(=C(C=C1NC(=S)NC2=C(C=CC(=C2)F)F)Cl)OC QCWAEKJCJNGXQY-UHFFFAOYSA-N 0.000 description 1
- NELYZUPALKKDFK-UHFFFAOYSA-N 1-(5-chloro-2,4-dimethoxyphenyl)-3-methylthiourea Chemical compound CNC(=S)NC1=CC(Cl)=C(OC)C=C1OC NELYZUPALKKDFK-UHFFFAOYSA-N 0.000 description 1
- PZZQUSYTIVCKGV-UHFFFAOYSA-N 1-(5-hydroxynaphthalen-1-yl)-3-phenylthiourea Chemical compound C1=CC=C2C(O)=CC=CC2=C1NC(=S)NC1=CC=CC=C1 PZZQUSYTIVCKGV-UHFFFAOYSA-N 0.000 description 1
- OYBLHGYAOANGML-UHFFFAOYSA-N 1-(6-methyl-4-oxo-1h-pyrimidin-2-yl)-3-[(2-nitrophenyl)methylidene]thiourea Chemical compound N1C(C)=CC(=O)N=C1NC(=S)N=CC1=CC=CC=C1[N+]([O-])=O OYBLHGYAOANGML-UHFFFAOYSA-N 0.000 description 1
- QMYDRQBPTKPRHP-UHFFFAOYSA-N 1-(azepan-1-yl)-3-[3-(trifluoromethyl)phenyl]thiourea Chemical compound FC(F)(F)C1=CC=CC(NC(=S)NN2CCCCCC2)=C1 QMYDRQBPTKPRHP-UHFFFAOYSA-N 0.000 description 1
- GDTGWBKXPIVHPW-UHFFFAOYSA-N 1-(diaminomethylidene)-3-(4-methylphenyl)thiourea Chemical compound CC1=CC=C(NC(=S)N=C(N)N)C=C1 GDTGWBKXPIVHPW-UHFFFAOYSA-N 0.000 description 1
- FDYJHOJSZVEPLV-UHFFFAOYSA-N 1-(diaminomethylidene)-3-methylthiourea;4-methylbenzenesulfonic acid Chemical compound CNC(=S)N=C(N)N.CC1=CC=C(S(O)(=O)=O)C=C1 FDYJHOJSZVEPLV-UHFFFAOYSA-N 0.000 description 1
- LPXNRJGSIDFGGQ-UHFFFAOYSA-N 1-(diaminomethylidene)-3-propylthiourea Chemical compound CCCNC(=S)N=C(N)N LPXNRJGSIDFGGQ-UHFFFAOYSA-N 0.000 description 1
- LFUFHZIUVFNLJB-UHFFFAOYSA-N 1-(diaminomethylidene)-3-propylthiourea;4-methylbenzenesulfonic acid Chemical compound CCCNC(=S)N=C(N)N.CC1=CC=C(S(O)(=O)=O)C=C1 LFUFHZIUVFNLJB-UHFFFAOYSA-N 0.000 description 1
- SMEKEGGVCJRXLM-UHFFFAOYSA-N 1-(furan-2-ylmethyl)-3-naphthalen-1-ylthiourea Chemical compound C=1C=CC2=CC=CC=C2C=1NC(=S)NCC1=CC=CO1 SMEKEGGVCJRXLM-UHFFFAOYSA-N 0.000 description 1
- RJZAQQXEFJDQTR-UHFFFAOYSA-N 1-(furan-2-ylmethyl)-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NCC1=CC=CO1 RJZAQQXEFJDQTR-UHFFFAOYSA-N 0.000 description 1
- CMTZABANHATOHB-UHFFFAOYSA-N 1-(oxolan-2-ylmethyl)-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NCC1CCCO1 CMTZABANHATOHB-UHFFFAOYSA-N 0.000 description 1
- MMWLSBJVPGRSBO-UHFFFAOYSA-N 1-(pyridin-3-ylmethyl)-3-[2-(trifluoromethyl)phenyl]thiourea Chemical compound FC(F)(F)C1=CC=CC=C1NC(=S)NCC1=CC=CN=C1 MMWLSBJVPGRSBO-UHFFFAOYSA-N 0.000 description 1
- MLUMUEODUSHWJR-UHFFFAOYSA-N 1-[(1,3-dioxo-4h-naphthalen-2-ylidene)methyl]-3-octadecylthiourea Chemical compound C1=CC=C2C(=O)C(=CNC(=S)NCCCCCCCCCCCCCCCCCC)C(=O)CC2=C1 MLUMUEODUSHWJR-UHFFFAOYSA-N 0.000 description 1
- VCPJAGAMWSFFIL-UHFFFAOYSA-N 1-[(2,4-dioxo-1h-quinolin-3-yl)methyl]-3-hexylthiourea Chemical compound C1=CC=C2C(=O)C(CNC(=S)NCCCCCC)C(=O)NC2=C1 VCPJAGAMWSFFIL-UHFFFAOYSA-N 0.000 description 1
- NHRINBDSTWWGNA-UHFFFAOYSA-N 1-[(2,4-dioxochromen-3-ylidene)methyl]-3-octadecylthiourea Chemical compound C1=CC=C2C(=O)C(=CNC(=S)NCCCCCCCCCCCCCCCCCC)C(=O)OC2=C1 NHRINBDSTWWGNA-UHFFFAOYSA-N 0.000 description 1
- GFZPEGJPBLZUOY-UHFFFAOYSA-N 1-[(2,4-dioxochromen-3-ylidene)methyl]-3-phenylthiourea Chemical compound O=C1OC2=CC=CC=C2C(=O)C1=CNC(=S)NC1=CC=CC=C1 GFZPEGJPBLZUOY-UHFFFAOYSA-N 0.000 description 1
- VLDQNOXMBIXCOU-UHFFFAOYSA-N 1-[(2-chlorophenyl)methyl]-3-cyclohexyl-1-methylthiourea Chemical compound C1CCCCC1NC(=S)N(C)CC1=CC=CC=C1Cl VLDQNOXMBIXCOU-UHFFFAOYSA-N 0.000 description 1
- JHPQQEFWDDUNQU-UHFFFAOYSA-N 1-[(3,5-dichlorophenyl)methyl]-3-phenylthiourea Chemical compound ClC1=CC(Cl)=CC(CNC(=S)NC=2C=CC=CC=2)=C1 JHPQQEFWDDUNQU-UHFFFAOYSA-N 0.000 description 1
- RQCYXGASZSMDOI-UHFFFAOYSA-N 1-[(3-chlorophenyl)methyl]-1-methyl-3-prop-2-enylthiourea Chemical compound C=CCNC(=S)N(C)CC1=CC=CC(Cl)=C1 RQCYXGASZSMDOI-UHFFFAOYSA-N 0.000 description 1
- CYGSXYUOPPKHAE-UHFFFAOYSA-N 1-[(3-chlorophenyl)methyl]-3-phenylthiourea Chemical compound ClC1=CC=CC(CNC(=S)NC=2C=CC=CC=2)=C1 CYGSXYUOPPKHAE-UHFFFAOYSA-N 0.000 description 1
- SZSDDDAUOSJJTO-UHFFFAOYSA-N 1-[(4-chlorophenyl)methylidene]-3-(6-methyl-4-oxo-1h-pyrimidin-2-yl)thiourea Chemical compound N1C(C)=CC(=O)N=C1NC(=S)N=CC1=CC=C(Cl)C=C1 SZSDDDAUOSJJTO-UHFFFAOYSA-N 0.000 description 1
- KYYMYUIAHXUHIT-UHFFFAOYSA-N 1-[(4-methoxyphenyl)methyl]-3-phenylthiourea Chemical compound C1=CC(OC)=CC=C1CNC(=S)NC1=CC=CC=C1 KYYMYUIAHXUHIT-UHFFFAOYSA-N 0.000 description 1
- BXQKFLQHLAVEHB-UHFFFAOYSA-N 1-[(4-methoxyphenyl)methylidene]-3-(6-methyl-4-oxo-1h-pyrimidin-2-yl)thiourea Chemical compound C1=CC(OC)=CC=C1C=NC(=S)NC1=NC(=O)C=C(C)N1 BXQKFLQHLAVEHB-UHFFFAOYSA-N 0.000 description 1
- YDKMUNICSUMECU-UHFFFAOYSA-N 1-[(4-methylphenyl)methyl]-3-phenylthiourea Chemical compound C1=CC(C)=CC=C1CNC(=S)NC1=CC=CC=C1 YDKMUNICSUMECU-UHFFFAOYSA-N 0.000 description 1
- MJSOQAJPLMZPDS-UHFFFAOYSA-N 1-[(5-bromo-2-methoxyphenyl)methyl]-3-phenyl-1-(4-propan-2-ylphenyl)thiourea Chemical compound COC1=CC=C(Br)C=C1CN(C=1C=CC(=CC=1)C(C)C)C(=S)NC1=CC=CC=C1 MJSOQAJPLMZPDS-UHFFFAOYSA-N 0.000 description 1
- IBQCMZANQFBKDL-UHFFFAOYSA-N 1-[(6-methyl-2,4-dioxopyran-3-ylidene)methyl]-1-phenylthiourea Chemical compound CC1=CC(=O)C(=CN(C2=CC=CC=C2)C(=S)N)C(=O)O1 IBQCMZANQFBKDL-UHFFFAOYSA-N 0.000 description 1
- CJSDAIJCUJJYKE-XQNSMLJCSA-N 1-[(e)-2-benzylsulfinyl-2-phenylethenyl]-3-(2,4-dimethylphenyl)thiourea Chemical compound CC1=CC(C)=CC=C1NC(=S)N\C=C(S(=O)CC=1C=CC=CC=1)/C1=CC=CC=C1 CJSDAIJCUJJYKE-XQNSMLJCSA-N 0.000 description 1
- XKXNSSGXGWFECQ-LTGZKZEYSA-N 1-[(e)-2-benzylsulfinyl-2-phenylethenyl]-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)N/C=C(\C=1C=CC=CC=1)S(=O)CC1=CC=CC=C1 XKXNSSGXGWFECQ-LTGZKZEYSA-N 0.000 description 1
- KSKQDDAPVQIFBM-UHFFFAOYSA-N 1-[2-(2-hydroxyethoxy)ethyl]-3-phenylthiourea Chemical compound OCCOCCNC(=S)NC1=CC=CC=C1 KSKQDDAPVQIFBM-UHFFFAOYSA-N 0.000 description 1
- OZMAFADSXYBINI-UHFFFAOYSA-N 1-[2-(2-oxopyrrolidin-1-yl)ethyl]-3-phenylthiourea Chemical compound O=C1CCCN1CCNC(=S)NC1=CC=CC=C1 OZMAFADSXYBINI-UHFFFAOYSA-N 0.000 description 1
- IYINLXVXEWSLLF-UHFFFAOYSA-N 1-[3-(dibutylamino)propyl]-3-phenylthiourea Chemical compound CCCCN(CCCC)CCCNC(=S)NC1=CC=CC=C1 IYINLXVXEWSLLF-UHFFFAOYSA-N 0.000 description 1
- VQAAMPPTIUBDBG-UHFFFAOYSA-N 1-[4,5-dimethyl-2-(phenylcarbamothioylamino)phenyl]-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC=1C=C(C)C(C)=CC=1NC(=S)NC1=CC=CC=C1 VQAAMPPTIUBDBG-UHFFFAOYSA-N 0.000 description 1
- URRDGSUZXIHVNL-UHFFFAOYSA-N 1-[4-(difluoromethoxy)-2-formylphenyl]-3-(3,3-dimethylbutan-2-yl)thiourea Chemical compound CC(C)(C)C(C)NC(=S)NC1=CC=C(OC(F)F)C=C1C=O URRDGSUZXIHVNL-UHFFFAOYSA-N 0.000 description 1
- YYSGVNYHHCLDSS-UHFFFAOYSA-N 1-[4-(difluoromethoxy)phenyl]-3-(3,3-dimethylbutan-2-yl)thiourea Chemical compound CC(C)(C)C(C)NC(=S)NC1=CC=C(OC(F)F)C=C1 YYSGVNYHHCLDSS-UHFFFAOYSA-N 0.000 description 1
- RDIJRRGZZARMTJ-UHFFFAOYSA-N 1-[4-(difluoromethylsulfanyl)phenyl]-3-(3,3-dimethylbutan-2-yl)thiourea Chemical compound CC(C)(C)C(C)NC(=S)NC1=CC=C(SC(F)F)C=C1 RDIJRRGZZARMTJ-UHFFFAOYSA-N 0.000 description 1
- ZTFJDQSUKGFENB-UHFFFAOYSA-N 1-[4-(dimethylamino)phenyl]-3-(4-nitrophenyl)thiourea Chemical compound C1=CC(N(C)C)=CC=C1NC(=S)NC1=CC=C([N+]([O-])=O)C=C1 ZTFJDQSUKGFENB-UHFFFAOYSA-N 0.000 description 1
- HABOTJOLVOHPAA-UHFFFAOYSA-N 1-[4-(dimethylamino)phenyl]-3-phenylthiourea Chemical compound C1=CC(N(C)C)=CC=C1NC(=S)NC1=CC=CC=C1 HABOTJOLVOHPAA-UHFFFAOYSA-N 0.000 description 1
- CEYAYMLGPATRGK-UHFFFAOYSA-N 1-[4-[(4-fluorophenyl)methylsulfanyl]phenyl]-3-(4-methoxyphenyl)thiourea Chemical compound C1=CC(OC)=CC=C1NC(=S)NC(C=C1)=CC=C1SCC1=CC=C(F)C=C1 CEYAYMLGPATRGK-UHFFFAOYSA-N 0.000 description 1
- YQBIVIRBVJOGQJ-UHFFFAOYSA-N 1-[5-(dimethylamino)naphthalen-1-yl]sulfonyl-3-ethylthiourea Chemical compound C1=CC=C2C(S(=O)(=O)NC(=S)NCC)=CC=CC2=C1N(C)C YQBIVIRBVJOGQJ-UHFFFAOYSA-N 0.000 description 1
- SRAXJVRQKOKBMO-UHFFFAOYSA-N 1-[anilino(phenyl)methylidene]-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(C=1C=CC=CC=1)=NC(=S)NC1=CC=CC=C1 SRAXJVRQKOKBMO-UHFFFAOYSA-N 0.000 description 1
- UFDUTRQZBZTJIH-UHFFFAOYSA-N 1-[n-(benzenesulfonylmethyl)-c-phenylcarbonimidoyl]-3-(4-fluorophenyl)thiourea Chemical compound C1=CC(F)=CC=C1NC(=S)NC(C=1C=CC=CC=1)=NCS(=O)(=O)C1=CC=CC=C1 UFDUTRQZBZTJIH-UHFFFAOYSA-N 0.000 description 1
- CDRUQTZDODYZCB-UHFFFAOYSA-N 1-[n-(benzenesulfonylmethyl)-c-phenylcarbonimidoyl]-3-(4-methylphenyl)thiourea Chemical compound C1=CC(C)=CC=C1NC(=S)NC(C=1C=CC=CC=1)=NCS(=O)(=O)C1=CC=CC=C1 CDRUQTZDODYZCB-UHFFFAOYSA-N 0.000 description 1
- GUUOYRKTCSPGKE-UHFFFAOYSA-N 1-benzhydryl-3-(2-phenylethyl)thiourea Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)NC(=S)NCCC1=CC=CC=C1 GUUOYRKTCSPGKE-UHFFFAOYSA-N 0.000 description 1
- NYXJXGLOVNXBBP-UHFFFAOYSA-N 1-benzhydryl-3-(3,4-dichlorophenyl)thiourea Chemical compound C1=C(Cl)C(Cl)=CC=C1NC(=S)NC(C=1C=CC=CC=1)C1=CC=CC=C1 NYXJXGLOVNXBBP-UHFFFAOYSA-N 0.000 description 1
- VDFUCSQUJYZLAZ-UHFFFAOYSA-N 1-benzyl-1-butyl-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)N(CCCC)CC1=CC=CC=C1 VDFUCSQUJYZLAZ-UHFFFAOYSA-N 0.000 description 1
- CIQFTOMAXKXLJP-UHFFFAOYSA-N 1-benzyl-1-ethyl-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)N(CC)CC1=CC=CC=C1 CIQFTOMAXKXLJP-UHFFFAOYSA-N 0.000 description 1
- PDHMEDMWKUZUAB-UHFFFAOYSA-N 1-benzyl-3-(1,3-thiazol-2-yl)thiourea Chemical compound N=1C=CSC=1NC(=S)NCC1=CC=CC=C1 PDHMEDMWKUZUAB-UHFFFAOYSA-N 0.000 description 1
- BOKAIGGNTVOWOJ-UHFFFAOYSA-N 1-benzyl-3-(4-fluoro-3-nitrophenyl)thiourea Chemical compound C1=C(F)C([N+](=O)[O-])=CC(NC(=S)NCC=2C=CC=CC=2)=C1 BOKAIGGNTVOWOJ-UHFFFAOYSA-N 0.000 description 1
- VFLJMXAJZZTHFU-UHFFFAOYSA-N 1-benzyl-3-(furan-2-ylmethyl)thiourea Chemical compound C=1C=CC=CC=1CNC(=S)NCC1=CC=CO1 VFLJMXAJZZTHFU-UHFFFAOYSA-N 0.000 description 1
- FMBUYXXEXPSPQS-UHFFFAOYSA-N 1-benzyl-3-[3-(4-bromophenyl)-5-sulfanylidene-1h-1,2,4-triazol-4-yl]thiourea Chemical compound C1=CC(Br)=CC=C1C1=NNC(=S)N1NC(=S)NCC1=CC=CC=C1 FMBUYXXEXPSPQS-UHFFFAOYSA-N 0.000 description 1
- DHOVKNXEOGJVQR-UHFFFAOYSA-N 1-benzyl-3-[4-chloro-2-(trifluoromethyl)phenyl]thiourea Chemical compound FC(F)(F)C1=CC(Cl)=CC=C1NC(=S)NCC1=CC=CC=C1 DHOVKNXEOGJVQR-UHFFFAOYSA-N 0.000 description 1
- PUZAABGCFWTNMH-UHFFFAOYSA-N 1-benzyl-3-cyclohexyl-1-ethyl-3-phenylthiourea Chemical compound CCN(CC1=CC=CC=C1)C(=S)N(C2CCCCC2)C3=CC=CC=C3 PUZAABGCFWTNMH-UHFFFAOYSA-N 0.000 description 1
- GDUBTTXVKWIAKV-UHFFFAOYSA-N 1-benzyl-3-methylthiourea Chemical compound CNC(=S)NCC1=CC=CC=C1 GDUBTTXVKWIAKV-UHFFFAOYSA-N 0.000 description 1
- KDXKGWLTZXBZDC-UHFFFAOYSA-N 1-benzyl-3-pyridin-2-ylthiourea Chemical compound C=1C=CC=NC=1NC(=S)NCC1=CC=CC=C1 KDXKGWLTZXBZDC-UHFFFAOYSA-N 0.000 description 1
- DXUHWIPNRRHGLQ-UHFFFAOYSA-N 1-but-3-en-2-yl-3-morpholin-4-ylthiourea Chemical compound C=CC(C)NC(=S)NN1CCOCC1 DXUHWIPNRRHGLQ-UHFFFAOYSA-N 0.000 description 1
- KKTZOAAEFNOGBS-UHFFFAOYSA-N 1-butyl-3-(4-propan-2-ylphenyl)thiourea Chemical compound CCCCNC(=S)NC1=CC=C(C(C)C)C=C1 KKTZOAAEFNOGBS-UHFFFAOYSA-N 0.000 description 1
- MXLMUGKRDLWVJZ-UHFFFAOYSA-N 1-butyl-3-phenylthiourea Chemical compound CCCCNC(=S)NC1=CC=CC=C1 MXLMUGKRDLWVJZ-UHFFFAOYSA-N 0.000 description 1
- LXYIUAPDEIGKQI-UHFFFAOYSA-N 1-butyl-3-pyridin-2-ylthiourea Chemical compound CCCCNC(=S)NC1=CC=CC=N1 LXYIUAPDEIGKQI-UHFFFAOYSA-N 0.000 description 1
- QIIQPLHVXQXRGY-UHFFFAOYSA-N 1-cyano-3-methylthiourea Chemical compound CNC(=S)NC#N QIIQPLHVXQXRGY-UHFFFAOYSA-N 0.000 description 1
- CAVLDGJVMTVLQJ-UHFFFAOYSA-N 1-cyclohexyl-1-methyl-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)N(C)C1CCCCC1 CAVLDGJVMTVLQJ-UHFFFAOYSA-N 0.000 description 1
- HENUXILFJOCRKP-UHFFFAOYSA-N 1-cyclohexyl-3-(1-phenylethyl)thiourea Chemical compound C=1C=CC=CC=1C(C)NC(=S)NC1CCCCC1 HENUXILFJOCRKP-UHFFFAOYSA-N 0.000 description 1
- CUUDOECMUOESMY-UHFFFAOYSA-N 1-cyclohexyl-3-(2-ethoxyphenyl)thiourea Chemical compound CCOC1=CC=CC=C1NC(=S)NC1CCCCC1 CUUDOECMUOESMY-UHFFFAOYSA-N 0.000 description 1
- AKYYGBUVZFGJNI-UHFFFAOYSA-N 1-cyclohexyl-3-(2-morpholin-4-ylethyl)thiourea Chemical compound C1CCCCC1NC(=S)NCCN1CCOCC1 AKYYGBUVZFGJNI-UHFFFAOYSA-N 0.000 description 1
- YVBXZPBYVNCHJU-UHFFFAOYSA-N 1-cyclohexyl-3-(4-ethoxyphenyl)thiourea Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC1CCCCC1 YVBXZPBYVNCHJU-UHFFFAOYSA-N 0.000 description 1
- PASBFQMDQRGJBH-UHFFFAOYSA-N 1-cyclohexyl-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1CCCCC1 PASBFQMDQRGJBH-UHFFFAOYSA-N 0.000 description 1
- LJVDCHOCLAEROU-UHFFFAOYSA-N 1-cyclopentyl-3-phenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1CCCC1 LJVDCHOCLAEROU-UHFFFAOYSA-N 0.000 description 1
- HNMJUSWQMKEQEV-UHFFFAOYSA-N 1-decyl-3-(2-hydroxyethyl)thiourea Chemical compound CCCCCCCCCCNC(=S)NCCO HNMJUSWQMKEQEV-UHFFFAOYSA-N 0.000 description 1
- UXXVTHRQMWWTIR-UHFFFAOYSA-N 1-dodecyl-3-phenylthiourea Chemical compound CCCCCCCCCCCCNC(=S)NC1=CC=CC=C1 UXXVTHRQMWWTIR-UHFFFAOYSA-N 0.000 description 1
- HFCRLSLRGLNPDK-UHFFFAOYSA-N 1-ethyl-3-(2-fluorophenyl)thiourea Chemical compound CCNC(=S)NC1=CC=CC=C1F HFCRLSLRGLNPDK-UHFFFAOYSA-N 0.000 description 1
- ZXUNCTJJCGQZPY-UHFFFAOYSA-N 1-ethyl-3-(2-methoxy-5-methylphenyl)thiourea Chemical compound CCNC(=S)NC1=CC(C)=CC=C1OC ZXUNCTJJCGQZPY-UHFFFAOYSA-N 0.000 description 1
- YDUGLSQPIVEIMP-UHFFFAOYSA-N 1-ethyl-3-(3-methylphenyl)thiourea Chemical compound CCNC(=S)NC1=CC=CC(C)=C1 YDUGLSQPIVEIMP-UHFFFAOYSA-N 0.000 description 1
- FNGYBATZKHIECN-UHFFFAOYSA-N 1-ethyl-3-(4-methylphenyl)thiourea Chemical compound CCNC(=S)NC1=CC=C(C)C=C1 FNGYBATZKHIECN-UHFFFAOYSA-N 0.000 description 1
- DRXNTJUGFANLMS-UHFFFAOYSA-N 1-ethyl-3-(4-nitrophenyl)thiourea Chemical compound CCNC(=S)NC1=CC=C([N+]([O-])=O)C=C1 DRXNTJUGFANLMS-UHFFFAOYSA-N 0.000 description 1
- OROCFDLTBPBLFS-UHFFFAOYSA-N 1-ethyl-3-phenylthiourea Chemical compound CCNC(=S)NC1=CC=CC=C1 OROCFDLTBPBLFS-UHFFFAOYSA-N 0.000 description 1
- AGGCPIHYQNXMTR-UHFFFAOYSA-N 1-hexadecyl-3-phenylthiourea Chemical compound CCCCCCCCCCCCCCCCNC(=S)NC1=CC=CC=C1 AGGCPIHYQNXMTR-UHFFFAOYSA-N 0.000 description 1
- ATBAJWHXPPLZNK-UHFFFAOYSA-N 1-methyl-1-(4-octoxyphenyl)thiourea Chemical compound CCCCCCCCOC1=CC=C(N(C)C(N)=S)C=C1 ATBAJWHXPPLZNK-UHFFFAOYSA-N 0.000 description 1
- FOGVXPRGYRQORO-UHFFFAOYSA-N 1-methyl-3-(2,4,5-trichlorophenyl)thiourea Chemical compound CNC(=S)NC1=CC(Cl)=C(Cl)C=C1Cl FOGVXPRGYRQORO-UHFFFAOYSA-N 0.000 description 1
- UUXUIXBWRPPCIS-UHFFFAOYSA-N 1-methyl-3-(2-methylprop-2-enyl)thiourea Chemical compound CNC(=S)NCC(C)=C UUXUIXBWRPPCIS-UHFFFAOYSA-N 0.000 description 1
- IGEQFPWPMCIYDF-UHFFFAOYSA-N 1-methyl-3-phenylthiourea Chemical compound CNC(=S)NC1=CC=CC=C1 IGEQFPWPMCIYDF-UHFFFAOYSA-N 0.000 description 1
- PRNKCKMGXDOUGR-UHFFFAOYSA-N 1-methyl-3-propylthiourea Chemical compound CCCNC(=S)NC PRNKCKMGXDOUGR-UHFFFAOYSA-N 0.000 description 1
- MZANDQOBAWDXBP-UHFFFAOYSA-N 1-morpholin-4-yl-3-prop-2-enylthiourea Chemical compound C=CCNC(=S)NN1CCOCC1 MZANDQOBAWDXBP-UHFFFAOYSA-N 0.000 description 1
- GGZCNPBFWWAIHK-UHFFFAOYSA-N 1-naphthalen-1-yl-3-propan-2-ylthiourea Chemical compound C1=CC=C2C(NC(=S)NC(C)C)=CC=CC2=C1 GGZCNPBFWWAIHK-UHFFFAOYSA-N 0.000 description 1
- IPJJRJZXOAMHLE-UHFFFAOYSA-N 1-naphthalen-2-yl-3-phenylthiourea Chemical compound C=1C=C2C=CC=CC2=CC=1NC(=S)NC1=CC=CC=C1 IPJJRJZXOAMHLE-UHFFFAOYSA-N 0.000 description 1
- RZIFSZUVDCQREY-UHFFFAOYSA-N 1-phenyl-3-(1,2,4-triazol-4-yl)thiourea Chemical compound C1=NN=CN1NC(=S)NC1=CC=CC=C1 RZIFSZUVDCQREY-UHFFFAOYSA-N 0.000 description 1
- GCZZOZBWAZHCAN-UHFFFAOYSA-N 1-phenyl-3-(1,3-thiazol-2-yl)thiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1=NC=CS1 GCZZOZBWAZHCAN-UHFFFAOYSA-N 0.000 description 1
- FOFYTAQBFPAROM-UHFFFAOYSA-N 1-phenyl-3-(2-pyridin-2-ylethyl)thiourea Chemical compound C=1C=CC=CC=1NC(=S)NCCC1=CC=CC=N1 FOFYTAQBFPAROM-UHFFFAOYSA-N 0.000 description 1
- ZCWIUNSNTFZNAQ-UHFFFAOYSA-N 1-phenyl-3-(5-phenyl-1,2,4-thiadiazol-3-yl)thiourea Chemical compound C=1C=CC=CC=1NC(=S)NC(N=1)=NSC=1C1=CC=CC=C1 ZCWIUNSNTFZNAQ-UHFFFAOYSA-N 0.000 description 1
- QFHALJZCNJGTFQ-UHFFFAOYSA-N 1-phenyl-3-(pyridin-3-ylmethyl)thiourea Chemical compound C=1C=CC=CC=1NC(=S)NCC1=CC=CN=C1 QFHALJZCNJGTFQ-UHFFFAOYSA-N 0.000 description 1
- XJJNEACGVXAQNE-UHFFFAOYSA-N 1-phenyl-3-[2-(phenylcarbamothioylamino)cyclohexyl]thiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1CCCCC1NC(=S)NC1=CC=CC=C1 XJJNEACGVXAQNE-UHFFFAOYSA-N 0.000 description 1
- CUUPMTYGTPOVMV-UHFFFAOYSA-N 1-phenyl-3-[4-(phenylcarbamothioylamino)phenyl]thiourea Chemical compound C=1C=C(NC(=S)NC=2C=CC=CC=2)C=CC=1NC(=S)NC1=CC=CC=C1 CUUPMTYGTPOVMV-UHFFFAOYSA-N 0.000 description 1
- MWSJUCRBEATBJT-UHFFFAOYSA-N 1-phenyl-3-[[4-(trifluoromethyl)phenyl]methyl]thiourea Chemical compound C1=CC(C(F)(F)F)=CC=C1CNC(=S)NC1=CC=CC=C1 MWSJUCRBEATBJT-UHFFFAOYSA-N 0.000 description 1
- RJTICPGQFMYYEG-UHFFFAOYSA-N 1-phenyl-3-prop-2-enylthiourea Chemical compound C=CCNC(=S)NC1=CC=CC=C1 RJTICPGQFMYYEG-UHFFFAOYSA-N 0.000 description 1
- LFBMRUOVWMEFFZ-UHFFFAOYSA-N 1-phenyl-3-propan-2-ylthiourea Chemical compound CC(C)NC(=S)NC1=CC=CC=C1 LFBMRUOVWMEFFZ-UHFFFAOYSA-N 0.000 description 1
- HZPCVTKJHKWEDX-UHFFFAOYSA-N 1-phenyl-3-propylthiourea Chemical compound CCCNC(=S)NC1=CC=CC=C1 HZPCVTKJHKWEDX-UHFFFAOYSA-N 0.000 description 1
- JFHXWMRFXORESD-UHFFFAOYSA-N 1-phenyl-3-pyridin-2-ylthiourea Chemical compound C=1C=CC=NC=1NC(=S)NC1=CC=CC=C1 JFHXWMRFXORESD-UHFFFAOYSA-N 0.000 description 1
- WEBCASPSGDNATE-UHFFFAOYSA-N 1-phenyl-3-pyridin-3-ylthiourea Chemical compound C=1C=CN=CC=1NC(=S)NC1=CC=CC=C1 WEBCASPSGDNATE-UHFFFAOYSA-N 0.000 description 1
- VYPUTGOCHAGRIZ-UHFFFAOYSA-N 1-phenyl-3-tetradecylthiourea Chemical compound CCCCCCCCCCCCCCNC(=S)NC1=CC=CC=C1 VYPUTGOCHAGRIZ-UHFFFAOYSA-N 0.000 description 1
- VPPYIQDUSLZZII-UHFFFAOYSA-N 1-phenylpropan-2-ylthiourea Chemical compound NC(=S)NC(C)CC1=CC=CC=C1 VPPYIQDUSLZZII-UHFFFAOYSA-N 0.000 description 1
- RBBBLQWHSSRHLG-UHFFFAOYSA-N 1-propan-2-yl-3-[3-(trifluoromethyl)phenyl]thiourea Chemical compound CC(C)NC(=S)NC1=CC=CC(C(F)(F)F)=C1 RBBBLQWHSSRHLG-UHFFFAOYSA-N 0.000 description 1
- CKGKBGDOTXJTGG-UHFFFAOYSA-N 1-tert-butyl-3-[3-(trifluoromethyl)phenyl]thiourea Chemical compound CC(C)(C)NC(=S)NC1=CC=CC(C(F)(F)F)=C1 CKGKBGDOTXJTGG-UHFFFAOYSA-N 0.000 description 1
- JHMCTNQTJNGVRX-UHFFFAOYSA-N 1-tert-butyl-3-phenylthiourea Chemical compound CC(C)(C)NC(=S)NC1=CC=CC=C1 JHMCTNQTJNGVRX-UHFFFAOYSA-N 0.000 description 1
- QPHHZCXEHPQYCJ-UHFFFAOYSA-N 2,2-dicyanoethenylthiourea Chemical compound NC(=S)NC=C(C#N)C#N QPHHZCXEHPQYCJ-UHFFFAOYSA-N 0.000 description 1
- VZYNWSUMPDNIOF-UHFFFAOYSA-N 2,2-dimethyl-n-[(2-nitrophenyl)carbamothioyl]propanamide Chemical compound CC(C)(C)C(=O)NC(=S)NC1=CC=CC=C1[N+]([O-])=O VZYNWSUMPDNIOF-UHFFFAOYSA-N 0.000 description 1
- IXZMSEDOTHHNPF-UHFFFAOYSA-N 2,3,4-trimethoxy-n-[[3-(trifluoromethyl)phenyl]carbamothioyl]benzamide Chemical compound COC1=C(OC)C(OC)=CC=C1C(=O)NC(=S)NC1=CC=CC(C(F)(F)F)=C1 IXZMSEDOTHHNPF-UHFFFAOYSA-N 0.000 description 1
- WOQACIUOGYPTNV-UHFFFAOYSA-N 2,4-dichloro-n-(dibenzylcarbamothioyl)benzamide Chemical compound ClC1=CC(Cl)=CC=C1C(=O)NC(=S)N(CC=1C=CC=CC=1)CC1=CC=CC=C1 WOQACIUOGYPTNV-UHFFFAOYSA-N 0.000 description 1
- FQKUABDEHKGRGS-UHFFFAOYSA-N 2,4-dichloro-n-(naphthalen-1-ylcarbamothioyl)benzamide Chemical compound ClC1=CC(Cl)=CC=C1C(=O)NC(=S)NC1=CC=CC2=CC=CC=C12 FQKUABDEHKGRGS-UHFFFAOYSA-N 0.000 description 1
- NFZZGKCXDMFYKZ-UHFFFAOYSA-N 2,4-dichloro-n-(oxolan-2-ylmethylcarbamothioyl)benzamide Chemical compound ClC1=CC(Cl)=CC=C1C(=O)NC(=S)NCC1OCCC1 NFZZGKCXDMFYKZ-UHFFFAOYSA-N 0.000 description 1
- LWHAQKKCNSMPOS-UHFFFAOYSA-N 2,4-dichloro-n-(pyridin-2-ylmethylcarbamothioyl)benzamide Chemical compound ClC1=CC(Cl)=CC=C1C(=O)NC(=S)NCC1=CC=CC=N1 LWHAQKKCNSMPOS-UHFFFAOYSA-N 0.000 description 1
- NVAXNSOBXDNALH-UHFFFAOYSA-N 2,4-dichloro-n-[(2-chlorophenyl)carbamothioyl]benzamide Chemical compound ClC1=CC(Cl)=CC=C1C(=O)NC(=S)NC1=CC=CC=C1Cl NVAXNSOBXDNALH-UHFFFAOYSA-N 0.000 description 1
- PXGCSXIRTUQWBJ-UHFFFAOYSA-N 2,4-dichloro-n-[(4-chlorophenyl)carbamothioyl]benzamide Chemical compound C1=CC(Cl)=CC=C1NC(=S)NC(=O)C1=CC=C(Cl)C=C1Cl PXGCSXIRTUQWBJ-UHFFFAOYSA-N 0.000 description 1
- BIGHPNWDKMLDJS-UHFFFAOYSA-N 2,4-dichloro-n-[(7-hydroxynaphthalen-1-yl)carbamothioyl]benzamide Chemical compound C12=CC(O)=CC=C2C=CC=C1NC(=S)NC(=O)C1=CC=C(Cl)C=C1Cl BIGHPNWDKMLDJS-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
- RMCCONIRBZIDTH-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 1,3-dioxo-2-benzofuran-5-carboxylate Chemical compound CC(=C)C(=O)OCCOC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 RMCCONIRBZIDTH-UHFFFAOYSA-N 0.000 description 1
- ODBPZDVSJCSMMF-UHFFFAOYSA-N 2-(4-chlorophenoxy)-n-[(2-nitrophenyl)carbamothioyl]acetamide Chemical compound [O-][N+](=O)C1=CC=CC=C1NC(=S)NC(=O)COC1=CC=C(Cl)C=C1 ODBPZDVSJCSMMF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 1
- UEKHZPDUBLCUHN-UHFFFAOYSA-N 2-[[3,5,5-trimethyl-6-[2-(2-methylprop-2-enoyloxy)ethoxycarbonylamino]hexyl]carbamoyloxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOC(=O)NCCC(C)CC(C)(C)CNC(=O)OCCOC(=O)C(C)=C UEKHZPDUBLCUHN-UHFFFAOYSA-N 0.000 description 1
- NWPCXGGYSQHQGM-UHFFFAOYSA-N 2-aminoethyl carbamimidothioate Chemical compound NCCSC(N)=N NWPCXGGYSQHQGM-UHFFFAOYSA-N 0.000 description 1
- WDQHKPFOYRVFOU-UHFFFAOYSA-N 2-bromo-n-(furan-2-ylmethylcarbamothioyl)benzamide Chemical compound BrC1=CC=CC=C1C(=O)NC(=S)NCC1=CC=CO1 WDQHKPFOYRVFOU-UHFFFAOYSA-N 0.000 description 1
- ILRCPKWTYRTYMV-UHFFFAOYSA-N 2-chloro-n-[(2,4-difluorophenyl)carbamothioyl]benzamide Chemical compound FC1=CC(F)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1Cl ILRCPKWTYRTYMV-UHFFFAOYSA-N 0.000 description 1
- KWPBQLZJUHBFLQ-UHFFFAOYSA-N 2-chloro-n-[(2,4-dimethoxyphenyl)carbamothioyl]benzamide Chemical compound COC1=CC(OC)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1Cl KWPBQLZJUHBFLQ-UHFFFAOYSA-N 0.000 description 1
- NRDBLSCGPIEZDE-UHFFFAOYSA-N 2-chloro-n-[(2-fluorophenyl)carbamothioyl]benzamide Chemical compound FC1=CC=CC=C1NC(=S)NC(=O)C1=CC=CC=C1Cl NRDBLSCGPIEZDE-UHFFFAOYSA-N 0.000 description 1
- PAVFBLGNVFOGMD-UHFFFAOYSA-N 2-chloro-n-[(2-methoxy-5-methylphenyl)carbamothioyl]benzamide Chemical compound COC1=CC=C(C)C=C1NC(=S)NC(=O)C1=CC=CC=C1Cl PAVFBLGNVFOGMD-UHFFFAOYSA-N 0.000 description 1
- YTWGUBREZYSPJU-UHFFFAOYSA-N 2-chloro-n-[(3,4-dichlorophenyl)carbamothioyl]benzamide Chemical compound C1=C(Cl)C(Cl)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1Cl YTWGUBREZYSPJU-UHFFFAOYSA-N 0.000 description 1
- BJCVHSSRAYRKJX-UHFFFAOYSA-N 2-chloro-n-[(3-chlorophenyl)carbamothioyl]benzamide Chemical compound ClC1=CC=CC(NC(=S)NC(=O)C=2C(=CC=CC=2)Cl)=C1 BJCVHSSRAYRKJX-UHFFFAOYSA-N 0.000 description 1
- NQFXRQOJKSOWEZ-UHFFFAOYSA-N 2-chloro-n-[(4-nitrophenyl)carbamothioyl]benzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC(=S)NC(=O)C1=CC=CC=C1Cl NQFXRQOJKSOWEZ-UHFFFAOYSA-N 0.000 description 1
- YZFOKEVPEOEUHM-UHFFFAOYSA-N 2-chloro-n-[(5-chloro-2-methoxyphenyl)carbamothioyl]benzamide Chemical compound COC1=CC=C(Cl)C=C1NC(=S)NC(=O)C1=CC=CC=C1Cl YZFOKEVPEOEUHM-UHFFFAOYSA-N 0.000 description 1
- 125000003541 2-chlorobenzoyl group Chemical group ClC1=C(C(=O)*)C=CC=C1 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- ABSHJWZFDFHKRH-UHFFFAOYSA-N 2-cyanoethyl carbamimidothioate Chemical compound NC(=N)SCCC#N ABSHJWZFDFHKRH-UHFFFAOYSA-N 0.000 description 1
- AUYIBOYLWPVHSP-UHFFFAOYSA-N 2-fluoro-n-[(4-fluorophenyl)carbamothioyl]benzamide Chemical compound C1=CC(F)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1F AUYIBOYLWPVHSP-UHFFFAOYSA-N 0.000 description 1
- MIRQGKQPLPBZQM-UHFFFAOYSA-N 2-hydroperoxy-2,4,4-trimethylpentane Chemical compound CC(C)(C)CC(C)(C)OO MIRQGKQPLPBZQM-UHFFFAOYSA-N 0.000 description 1
- VJUCPHFOQJSDGQ-UHFFFAOYSA-N 2-hydroperoxypentylbenzene Chemical compound CCCC(OO)CC1=CC=CC=C1 VJUCPHFOQJSDGQ-UHFFFAOYSA-N 0.000 description 1
- LYCHQCXANCLPED-UHFFFAOYSA-N 2-hydroxy-3-methanimidoylbenzoic acid Chemical compound OC(=O)c1cccc(C=N)c1O LYCHQCXANCLPED-UHFFFAOYSA-N 0.000 description 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 1
- BLCRHWOMPOZAPR-UHFFFAOYSA-N 2-methyl-n-(phenylcarbamothioyl)benzamide Chemical compound CC1=CC=CC=C1C(=O)NC(=S)NC1=CC=CC=C1 BLCRHWOMPOZAPR-UHFFFAOYSA-N 0.000 description 1
- XOEPKIVHZOAKTP-UHFFFAOYSA-N 2-methyl-n-(pyridin-2-ylcarbamothioyl)benzamide Chemical compound CC1=CC=CC=C1C(=O)NC(=S)NC1=CC=CC=N1 XOEPKIVHZOAKTP-UHFFFAOYSA-N 0.000 description 1
- KGFVHZKXNIFXQC-UHFFFAOYSA-N 2-methyl-n-(pyrimidin-2-ylcarbamothioyl)benzamide Chemical compound CC1=CC=CC=C1C(=O)NC(=S)NC1=NC=CC=N1 KGFVHZKXNIFXQC-UHFFFAOYSA-N 0.000 description 1
- QXFXEDBUBQXEDH-UHFFFAOYSA-N 2-methyl-n-[(4-methylphenyl)carbamothioyl]benzamide Chemical compound C1=CC(C)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1C QXFXEDBUBQXEDH-UHFFFAOYSA-N 0.000 description 1
- OXZPUAQOAMTNNM-UHFFFAOYSA-N 2-methyl-n-[[4-(trifluoromethyl)phenyl]carbamothioyl]furan-3-carboxamide Chemical compound O1C=CC(C(=O)NC(=S)NC=2C=CC(=CC=2)C(F)(F)F)=C1C OXZPUAQOAMTNNM-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
- RGTMILHZLXZRGF-UHFFFAOYSA-N 2-methylpropylthiourea Chemical compound CC(C)CNC(N)=S RGTMILHZLXZRGF-UHFFFAOYSA-N 0.000 description 1
- HCPZNXBNGGSKGM-UHFFFAOYSA-N 3,4-dichloro-n-(1,3-thiazol-2-ylcarbamothioyl)benzamide Chemical compound C1=C(Cl)C(Cl)=CC=C1C(=O)NC(=S)NC1=NC=CS1 HCPZNXBNGGSKGM-UHFFFAOYSA-N 0.000 description 1
- PIKCJPRMBUKWAP-UHFFFAOYSA-N 3,4-dichloro-n-[(2-fluorophenyl)carbamothioyl]benzamide Chemical compound FC1=CC=CC=C1NC(=S)NC(=O)C1=CC=C(Cl)C(Cl)=C1 PIKCJPRMBUKWAP-UHFFFAOYSA-N 0.000 description 1
- RYCIQDGMQMNRPY-UHFFFAOYSA-N 3,4-dichloro-n-[(3,4-dichlorophenyl)carbamothioyl]benzamide Chemical compound C1=C(Cl)C(Cl)=CC=C1NC(=S)NC(=O)C1=CC=C(Cl)C(Cl)=C1 RYCIQDGMQMNRPY-UHFFFAOYSA-N 0.000 description 1
- WLAQUMHXLSWSGU-UHFFFAOYSA-N 3,4-dichloro-n-[(3-chlorophenyl)carbamothioyl]benzamide Chemical compound ClC1=CC=CC(NC(=S)NC(=O)C=2C=C(Cl)C(Cl)=CC=2)=C1 WLAQUMHXLSWSGU-UHFFFAOYSA-N 0.000 description 1
- NXTRMGWLWDZGFY-UHFFFAOYSA-N 3,4-dichloro-n-[(4-ethoxyphenyl)carbamothioyl]benzamide Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC(=O)C1=CC=C(Cl)C(Cl)=C1 NXTRMGWLWDZGFY-UHFFFAOYSA-N 0.000 description 1
- APNCBMYTNABWDE-UHFFFAOYSA-N 3,4-dichloro-n-[(4-nitrophenyl)carbamothioyl]benzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC(=S)NC(=O)C1=CC=C(Cl)C(Cl)=C1 APNCBMYTNABWDE-UHFFFAOYSA-N 0.000 description 1
- MMZABTLXRTYXIT-UHFFFAOYSA-N 3,4-dichloro-n-[(4-sulfamoylphenyl)carbamothioyl]benzamide Chemical compound C1=CC(S(=O)(=O)N)=CC=C1NC(=S)NC(=O)C1=CC=C(Cl)C(Cl)=C1 MMZABTLXRTYXIT-UHFFFAOYSA-N 0.000 description 1
- DWXICEYPPSOLFW-UHFFFAOYSA-N 3-(1,3-dimethyl-2,4-dioxopyrimidin-5-yl)-1,1-dimethylthiourea Chemical compound CN(C)C(=S)NC1=CN(C)C(=O)N(C)C1=O DWXICEYPPSOLFW-UHFFFAOYSA-N 0.000 description 1
- VHCHCRBADVQVIM-UHFFFAOYSA-N 3-(2,6-dimethylphenyl)-1,1-dimethylthiourea Chemical compound CN(C)C(=S)NC1=C(C)C=CC=C1C VHCHCRBADVQVIM-UHFFFAOYSA-N 0.000 description 1
- VAFQCBXEPSYWGI-UHFFFAOYSA-N 3-(2-methoxyphenyl)-1,1-dimethylthiourea Chemical compound COC1=CC=CC=C1NC(=S)N(C)C VAFQCBXEPSYWGI-UHFFFAOYSA-N 0.000 description 1
- WFIGMVFPEZTTAO-UHFFFAOYSA-N 3-(3,4-dimethylphenyl)-1,1-dimethylthiourea Chemical compound CN(C)C(=S)NC1=CC=C(C)C(C)=C1 WFIGMVFPEZTTAO-UHFFFAOYSA-N 0.000 description 1
- FWGDAHLBEXSAPT-UHFFFAOYSA-N 3-(4-chlorophenyl)-1,1-dimethylthiourea Chemical compound CN(C)C(=S)NC1=CC=C(Cl)C=C1 FWGDAHLBEXSAPT-UHFFFAOYSA-N 0.000 description 1
- BUWULXOJLGNTGU-UHFFFAOYSA-N 3-(4-ethoxyphenyl)-1,1-dimethylthiourea Chemical compound CCOC1=CC=C(NC(=S)N(C)C)C=C1 BUWULXOJLGNTGU-UHFFFAOYSA-N 0.000 description 1
- JPDXJCNMWXNPGV-UHFFFAOYSA-N 3-(4-methoxyphenyl)-1,1-dimethylthiourea Chemical compound COC1=CC=C(NC(=S)N(C)C)C=C1 JPDXJCNMWXNPGV-UHFFFAOYSA-N 0.000 description 1
- XQLYNFYPHOKNSF-UHFFFAOYSA-N 3-(5-chloro-2,4-dimethoxyphenyl)-1-(2-fluorophenyl)-1-methylthiourea Chemical compound C1=C(Cl)C(OC)=CC(OC)=C1NC(=S)N(C)C1=CC=CC=C1F XQLYNFYPHOKNSF-UHFFFAOYSA-N 0.000 description 1
- QCGUXRFTJDHKTF-UHFFFAOYSA-N 3-(dimethylamino)propylthiourea Chemical compound CN(C)CCCNC(N)=S QCGUXRFTJDHKTF-UHFFFAOYSA-N 0.000 description 1
- VPDYKJIPMXSKGA-UHFFFAOYSA-N 3-[(4-chlorophenyl)methyl]-1-methyl-1-phenylthiourea Chemical compound CN(C(=S)NCc1ccc(Cl)cc1)c1ccccc1 VPDYKJIPMXSKGA-UHFFFAOYSA-N 0.000 description 1
- OWEREODHYRUNQY-UHFFFAOYSA-N 3-bromo-n-[(3-chlorophenyl)carbamothioyl]benzamide Chemical compound ClC1=CC=CC(NC(=S)NC(=O)C=2C=C(Br)C=CC=2)=C1 OWEREODHYRUNQY-UHFFFAOYSA-N 0.000 description 1
- QDYUAZPBNLZIHG-CMDGGOBGSA-N 3-bromo-n-[[5-[(e)-3-(3-bromophenyl)prop-2-enoyl]-4-methyl-1,3-thiazol-2-yl]carbamothioyl]benzamide Chemical compound S1C(C(=O)\C=C\C=2C=C(Br)C=CC=2)=C(C)N=C1NC(=S)NC(=O)C1=CC=CC(Br)=C1 QDYUAZPBNLZIHG-CMDGGOBGSA-N 0.000 description 1
- BOZUZZFYEZILJL-UHFFFAOYSA-N 3-chloro-n-[(4-nitrophenyl)carbamothioyl]-1-benzothiophene-2-carboxamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC(=S)NC(=O)C1=C(Cl)C2=CC=CC=C2S1 BOZUZZFYEZILJL-UHFFFAOYSA-N 0.000 description 1
- RQQYMIYZTDXXRP-UHFFFAOYSA-N 3-cyclohexyl-1,1-bis(2-methylpropyl)thiourea Chemical compound CC(C)CN(CC(C)C)C(=S)NC1CCCCC1 RQQYMIYZTDXXRP-UHFFFAOYSA-N 0.000 description 1
- UCIVTQRTHNSZFO-UHFFFAOYSA-N 3-methoxy-N-(phenylcarbamothioyl)but-2-enamide Chemical compound CC(=CC(=O)NC(=S)NC1=CC=CC=C1)OC UCIVTQRTHNSZFO-UHFFFAOYSA-N 0.000 description 1
- FDWYDCXQLVOMPE-UHFFFAOYSA-N 3-methoxypropylthiourea Chemical compound COCCCNC(N)=S FDWYDCXQLVOMPE-UHFFFAOYSA-N 0.000 description 1
- PCCXHPASHLYGAC-UHFFFAOYSA-N 3-methyl-n-[(4-methylphenyl)carbamothioyl]furan-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C=CC(C)=CC=2)=C1C PCCXHPASHLYGAC-UHFFFAOYSA-N 0.000 description 1
- SCOVBZRUGCGTKD-UHFFFAOYSA-N 3-methyl-n-[[3-(trifluoromethyl)phenyl]carbamothioyl]furan-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C=C(C=CC=2)C(F)(F)F)=C1C SCOVBZRUGCGTKD-UHFFFAOYSA-N 0.000 description 1
- ZXRUTWUSBSDOCM-UHFFFAOYSA-N 3-methyl-n-[[4-(trifluoromethyl)phenyl]carbamothioyl]furan-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C=CC(=CC=2)C(F)(F)F)=C1C ZXRUTWUSBSDOCM-UHFFFAOYSA-N 0.000 description 1
- ROCDAFMDZLDGDA-UHFFFAOYSA-N 3-phenyl-1,1-di(propan-2-yl)thiourea Chemical compound CC(C)N(C(C)C)C(=S)NC1=CC=CC=C1 ROCDAFMDZLDGDA-UHFFFAOYSA-N 0.000 description 1
- KDZPENUZEKSMDE-UHFFFAOYSA-N 3-phenyl-1,1-dipropylthiourea Chemical compound CCCN(CCC)C(=S)NC1=CC=CC=C1 KDZPENUZEKSMDE-UHFFFAOYSA-N 0.000 description 1
- NZMPACDSYWNRIW-UHFFFAOYSA-N 3-phenylbutyl carbamimidothioate Chemical compound NC(=N)SCCC(C)C1=CC=CC=C1 NZMPACDSYWNRIW-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- NYYSPVRERVXMLJ-UHFFFAOYSA-N 4,4-difluorocyclohexan-1-one Chemical compound FC1(F)CCC(=O)CC1 NYYSPVRERVXMLJ-UHFFFAOYSA-N 0.000 description 1
- FOYDMXZTPAEILY-UHFFFAOYSA-N 4-(carbamothioylamino)benzoic acid Chemical compound NC(=S)NC1=CC=C(C(O)=O)C=C1 FOYDMXZTPAEILY-UHFFFAOYSA-N 0.000 description 1
- YZKFAIKNFGGKER-UHFFFAOYSA-N 4-(phenylcarbamothioylamino)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1NC(=S)NC1=CC=CC=C1 YZKFAIKNFGGKER-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 description 1
- WAUSIMAGUUSSKM-UHFFFAOYSA-N 4-methyl-n-[(4-piperidin-1-ylphenyl)carbamothioyl]benzamide Chemical compound C1=CC(C)=CC=C1C(=O)NC(=S)NC1=CC=C(N2CCCCC2)C=C1 WAUSIMAGUUSSKM-UHFFFAOYSA-N 0.000 description 1
- PIDBMNPCPAEPCX-UHFFFAOYSA-N 4-methylbenzenesulfonic acid;thiourea Chemical compound NC(S)=[NH2+].CC1=CC=C(S([O-])(=O)=O)C=C1 PIDBMNPCPAEPCX-UHFFFAOYSA-N 0.000 description 1
- NQAZUJLIKXAPOW-UHFFFAOYSA-N 4-nitro-n-(1,3-thiazol-2-ylcarbamothioyl)benzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)NC(=S)NC1=NC=CS1 NQAZUJLIKXAPOW-UHFFFAOYSA-N 0.000 description 1
- HNNNQTMVOODZJF-UHFFFAOYSA-N 4-nitro-n-(pyridin-2-ylmethylcarbamothioyl)benzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)NC(=S)NCC1=CC=CC=N1 HNNNQTMVOODZJF-UHFFFAOYSA-N 0.000 description 1
- OBZOTQJIUPWICF-UHFFFAOYSA-N 4-nitro-n-[(4-nitrophenyl)carbamothioyl]benzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC(=S)NC(=O)C1=CC=C([N+]([O-])=O)C=C1 OBZOTQJIUPWICF-UHFFFAOYSA-N 0.000 description 1
- UVEIBTOHNNCCPH-UHFFFAOYSA-N 5-[[6-(4-carboxypent-3-enoxycarbonylamino)-3,5,5-trimethylhexyl]carbamoyloxy]-2-methylpent-2-enoic acid Chemical compound CC(CCNC(=O)OCCC=C(C)C(=O)O)CC(C)(C)CNC(=O)OCCC=C(C)C(=O)O UVEIBTOHNNCCPH-UHFFFAOYSA-N 0.000 description 1
- DUCKJIOVQOAWEM-UHFFFAOYSA-N 5-methyl-n-[[2-(trifluoromethyl)phenyl]carbamothioyl]furan-2-carboxamide Chemical compound O1C(C)=CC=C1C(=O)NC(=S)NC1=CC=CC=C1C(F)(F)F DUCKJIOVQOAWEM-UHFFFAOYSA-N 0.000 description 1
- PIVQQUNOTICCSA-UHFFFAOYSA-N ANTU Chemical compound C1=CC=C2C(NC(=S)N)=CC=CC2=C1 PIVQQUNOTICCSA-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 1
- PXKLMJQFEQBVLD-UHFFFAOYSA-N Bisphenol F Natural products C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 1
- XBKBWWSWUUHJPG-UHFFFAOYSA-N C1=CC=C(C=C1)CCN=C(C2=CC=CC=C2)NC(=S)NCC3=CC=CC=C3 Chemical compound C1=CC=C(C=C1)CCN=C(C2=CC=CC=C2)NC(=S)NCC3=CC=CC=C3 XBKBWWSWUUHJPG-UHFFFAOYSA-N 0.000 description 1
- GTLBOCVHPBYCSX-UHFFFAOYSA-N CC(=O)OSC(=N)N Chemical compound CC(=O)OSC(=N)N GTLBOCVHPBYCSX-UHFFFAOYSA-N 0.000 description 1
- MGOPDWFPFDLFOP-UHFFFAOYSA-N CCC(C)(C(C(C)(C)C)OO)OO Chemical compound CCC(C)(C(C(C)(C)C)OO)OO MGOPDWFPFDLFOP-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- MMCJEAKINANSOL-UHFFFAOYSA-N Methiuron Chemical compound CN(C)C(=S)NC1=CC=CC(C)=C1 MMCJEAKINANSOL-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- VLCDUOXHFNUCKK-UHFFFAOYSA-N N,N'-Dimethylthiourea Chemical compound CNC(=S)NC VLCDUOXHFNUCKK-UHFFFAOYSA-N 0.000 description 1
- KFFQABQEJATQAT-UHFFFAOYSA-N N,N'-dibutylthiourea Chemical compound CCCCNC(=S)NCCCC KFFQABQEJATQAT-UHFFFAOYSA-N 0.000 description 1
- FLVIGYVXZHLUHP-UHFFFAOYSA-N N,N'-diethylthiourea Chemical compound CCNC(=S)NCC FLVIGYVXZHLUHP-UHFFFAOYSA-N 0.000 description 1
- GSPJGKYIHVSWAE-UHFFFAOYSA-N N-[(2,4-dichlorophenyl)carbamothioyl]-3-methylfuran-2-carboxamide Chemical compound CC1=C(OC=C1)C(=O)NC(=S)NC2=C(C=C(C=C2)Cl)Cl GSPJGKYIHVSWAE-UHFFFAOYSA-N 0.000 description 1
- RPRRLHORVDTJPU-UHFFFAOYSA-N N-[(2,4-dimethylphenyl)carbamothioyl]-2-methyl-3H-furan-2-carboxamide Chemical compound CC1=CC(=C(C=C1)NC(=S)NC(=O)C2(CC=CO2)C)C RPRRLHORVDTJPU-UHFFFAOYSA-N 0.000 description 1
- WDXVCWRYOTUJFL-UHFFFAOYSA-N N-[(4-iodophenyl)carbamothioyl]-3-phenoxypropanamide Chemical compound C1=CC=C(C=C1)OCCC(=O)NC(=S)NC2=CC=C(C=C2)I WDXVCWRYOTUJFL-UHFFFAOYSA-N 0.000 description 1
- QJFGYRVQWWFCBR-UHFFFAOYSA-N N-[[3-(4-chlorophenyl)-2-methylphenyl]carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=CC(=C1C)C2=CC=C(C=C2)Cl QJFGYRVQWWFCBR-UHFFFAOYSA-N 0.000 description 1
- SGICXMREVJZYQS-UHFFFAOYSA-N N-[ethyl(phenyl)carbamothioyl]-3-methoxybut-2-enamide Chemical compound CCN(C1=CC=CC=C1)C(=S)NC(=O)C=C(C)OC SGICXMREVJZYQS-UHFFFAOYSA-N 0.000 description 1
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- UHGKYJXJYJWDAM-UHFFFAOYSA-N Propylthiourea Chemical compound CCCNC(N)=S UHGKYJXJYJWDAM-UHFFFAOYSA-N 0.000 description 1
- MNOILHPDHOHILI-UHFFFAOYSA-N Tetramethylthiourea Chemical compound CN(C)C(=S)N(C)C MNOILHPDHOHILI-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- YMLZORCEPSBOKV-UHFFFAOYSA-N [2-(2,4-dichlorophenyl)-2-[(2,4-dichlorophenyl)methylsulfonyl]ethenyl]thiourea Chemical compound C=1C=C(Cl)C=C(Cl)C=1CS(=O)(=O)C(=CNC(=S)N)C1=CC=C(Cl)C=C1Cl YMLZORCEPSBOKV-UHFFFAOYSA-N 0.000 description 1
- ZUSWDTWYONAOPH-UHFFFAOYSA-N [2-(trifluoromethyl)phenyl]hydrazine;hydrochloride Chemical group [Cl-].[NH3+]NC1=CC=CC=C1C(F)(F)F ZUSWDTWYONAOPH-UHFFFAOYSA-N 0.000 description 1
- NHSYOVVWWKSDOS-UHFFFAOYSA-N [5-(2,4-dichlorophenyl)-1,3,4-oxadiazol-2-yl]thiourea Chemical compound O1C(NC(=S)N)=NN=C1C1=CC=C(Cl)C=C1Cl NHSYOVVWWKSDOS-UHFFFAOYSA-N 0.000 description 1
- KXHAVVUAJIISJN-UHFFFAOYSA-N [5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]thiourea Chemical compound C1=CC(OC)=CC=C1C1=NN=C(NC(N)=S)O1 KXHAVVUAJIISJN-UHFFFAOYSA-N 0.000 description 1
- GFTWGHKGIOUPKJ-UHFFFAOYSA-N [5-(phenoxymethyl)-1,3,4-oxadiazol-2-yl]thiourea Chemical compound O1C(NC(=S)N)=NN=C1COC1=CC=CC=C1 GFTWGHKGIOUPKJ-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- YFXFDZKYCRAMCM-UHFFFAOYSA-N [amino(2-aminoethylsulfanyl)methylidene]azanium;bromide Chemical compound Br.NCCSC(N)=N YFXFDZKYCRAMCM-UHFFFAOYSA-N 0.000 description 1
- YEDWMNOEZVHVMT-UHFFFAOYSA-N [anilino(phenyl)methylidene]thiourea Chemical compound C=1C=CC=CC=1C(=NC(=S)N)NC1=CC=CC=C1 YEDWMNOEZVHVMT-UHFFFAOYSA-N 0.000 description 1
- 238000010669 acid-base reaction Methods 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- HTKFORQRBXIQHD-UHFFFAOYSA-N allylthiourea Chemical compound NC(=S)NCC=C HTKFORQRBXIQHD-UHFFFAOYSA-N 0.000 description 1
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical group O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052916 barium silicate Inorganic materials 0.000 description 1
- HMOQPOVBDRFNIU-UHFFFAOYSA-N barium(2+);dioxido(oxo)silane Chemical compound [Ba+2].[O-][Si]([O-])=O HMOQPOVBDRFNIU-UHFFFAOYSA-N 0.000 description 1
- FYABMGZBIRRBQY-UHFFFAOYSA-N benzene;hydrogen peroxide Chemical compound OO.C1=CC=CC=C1 FYABMGZBIRRBQY-UHFFFAOYSA-N 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical group C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- GTRLQRHWPXEBLF-UHFFFAOYSA-N benzyl carbamimidothioate Chemical compound NC(=N)SCC1=CC=CC=C1 GTRLQRHWPXEBLF-UHFFFAOYSA-N 0.000 description 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
- UCGFRIAOVLXVKL-UHFFFAOYSA-N benzylthiourea Chemical compound NC(=S)NCC1=CC=CC=C1 UCGFRIAOVLXVKL-UHFFFAOYSA-N 0.000 description 1
- 229940106691 bisphenol a Drugs 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- ZKXWKVVCCTZOLD-UHFFFAOYSA-N copper;4-hydroxypent-3-en-2-one Chemical compound [Cu].CC(O)=CC(C)=O.CC(O)=CC(C)=O ZKXWKVVCCTZOLD-UHFFFAOYSA-N 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003479 dental cement Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- OWLFRUVJKUWJHF-UHFFFAOYSA-N diaminomethylidenethiourea;oxalic acid Chemical compound OC(=O)C(O)=O.NC(N)=NC(N)=S OWLFRUVJKUWJHF-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 1
- WIGNKAZCTOXTLY-UHFFFAOYSA-N ethyl 4-(ethylcarbamothioylamino)benzoate Chemical compound CCNC(=S)NC1=CC=C(C(=O)OCC)C=C1 WIGNKAZCTOXTLY-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- 239000002241 glass-ceramic Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- SDDKIZNHOCEXTF-UHFFFAOYSA-N methyl carbamimidothioate Chemical compound CSC(N)=N SDDKIZNHOCEXTF-UHFFFAOYSA-N 0.000 description 1
- OZWPDDIBWGQDBZ-UHFFFAOYSA-N n-(2,3-dihydro-1,4-benzodioxin-3-ylmethylcarbamothioyl)-4-methylbenzamide Chemical compound C1=CC(C)=CC=C1C(=O)NC(=S)NCC1OC2=CC=CC=C2OC1 OZWPDDIBWGQDBZ-UHFFFAOYSA-N 0.000 description 1
- OFJIRGSYJFNHRJ-UHFFFAOYSA-N n-(benzylcarbamothioyl)-2-methylbenzamide Chemical compound CC1=CC=CC=C1C(=O)NC(=S)NCC1=CC=CC=C1 OFJIRGSYJFNHRJ-UHFFFAOYSA-N 0.000 description 1
- XJPVBBYAUVZIDK-UHFFFAOYSA-N n-(benzylcarbamothioyl)-2-phenoxypropanamide Chemical compound C=1C=CC=CC=1CNC(=S)NC(=O)C(C)OC1=CC=CC=C1 XJPVBBYAUVZIDK-UHFFFAOYSA-N 0.000 description 1
- RONMPHKSKPPWFP-UHFFFAOYSA-N n-(diaminomethylidenecarbamothioyl)benzamide Chemical compound NC(N)=NC(=S)NC(=O)C1=CC=CC=C1 RONMPHKSKPPWFP-UHFFFAOYSA-N 0.000 description 1
- VCYBYFJHFVDRMU-UHFFFAOYSA-N n-(diethylcarbamothioyl)adamantane-1-carboxamide Chemical compound C1C(C2)CC3CC2CC1(C(=O)NC(=S)N(CC)CC)C3 VCYBYFJHFVDRMU-UHFFFAOYSA-N 0.000 description 1
- UQXSQVXCEQMCPC-UHFFFAOYSA-N n-(diethylcarbamothioyl)benzamide Chemical compound CCN(CC)C(=S)NC(=O)C1=CC=CC=C1 UQXSQVXCEQMCPC-UHFFFAOYSA-N 0.000 description 1
- VNOQULZQRFQPDR-UHFFFAOYSA-N n-(dihexylcarbamothioyl)benzamide Chemical compound CCCCCCN(CCCCCC)C(=S)NC(=O)C1=CC=CC=C1 VNOQULZQRFQPDR-UHFFFAOYSA-N 0.000 description 1
- ZTTJSQVQVIRUQD-UHFFFAOYSA-N n-(furan-2-ylmethylcarbamothioyl)-2-methylbenzamide Chemical compound CC1=CC=CC=C1C(=O)NC(=S)NCC1=CC=CO1 ZTTJSQVQVIRUQD-UHFFFAOYSA-N 0.000 description 1
- VKDNHTHTZNCNNS-UHFFFAOYSA-N n-(furan-2-ylmethylcarbamothioyl)-4-nitrobenzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)NC(=S)NCC1=CC=CO1 VKDNHTHTZNCNNS-UHFFFAOYSA-N 0.000 description 1
- KLCUTYGLJDBNKU-UHFFFAOYSA-N n-(furan-2-ylmethylcarbamothioyl)furan-2-carboxamide Chemical compound C=1C=COC=1C(=O)NC(=S)NCC1=CC=CO1 KLCUTYGLJDBNKU-UHFFFAOYSA-N 0.000 description 1
- BSRSEAYGGXWBAB-UHFFFAOYSA-N n-(n'-carbamothioylcarbamimidoyl)benzamide Chemical compound NC(=S)N=C(N)NC(=O)C1=CC=CC=C1 BSRSEAYGGXWBAB-UHFFFAOYSA-N 0.000 description 1
- OLTKAJNSDSFRBL-UHFFFAOYSA-N n-(naphthalen-1-ylcarbamothioyl)-2-phenoxypropanamide Chemical compound C=1C=CC2=CC=CC=C2C=1NC(=S)NC(=O)C(C)OC1=CC=CC=C1 OLTKAJNSDSFRBL-UHFFFAOYSA-N 0.000 description 1
- JYZHKZNALZZENK-UHFFFAOYSA-N n-(naphthalen-1-ylcarbamothioyl)benzamide Chemical compound C=1C=CC2=CC=CC=C2C=1NC(=S)NC(=O)C1=CC=CC=C1 JYZHKZNALZZENK-UHFFFAOYSA-N 0.000 description 1
- YVUHGCPWEFAJTA-UHFFFAOYSA-N n-(naphthalen-1-ylcarbamothioyl)dodecanamide Chemical compound C1=CC=C2C(NC(=S)NC(=O)CCCCCCCCCCC)=CC=CC2=C1 YVUHGCPWEFAJTA-UHFFFAOYSA-N 0.000 description 1
- UBTRNYDBOADCHD-UHFFFAOYSA-N n-(naphthalen-2-ylcarbamothioyl)dodecanamide Chemical compound C1=CC=CC2=CC(NC(=S)NC(=O)CCCCCCCCCCC)=CC=C21 UBTRNYDBOADCHD-UHFFFAOYSA-N 0.000 description 1
- DBOBDMZHSHKLSJ-UHFFFAOYSA-N n-(phenylcarbamothioyl)acetamide Chemical compound CC(=O)NC(=S)NC1=CC=CC=C1 DBOBDMZHSHKLSJ-UHFFFAOYSA-N 0.000 description 1
- GVHZQIIMGRLFMX-UHFFFAOYSA-N n-(phenylcarbamothioyl)benzamide Chemical compound C=1C=CC=CC=1C(=O)NC(=S)NC1=CC=CC=C1 GVHZQIIMGRLFMX-UHFFFAOYSA-N 0.000 description 1
- AYYNLNBVTNAZEG-UHFFFAOYSA-N n-(pyridin-2-ylmethylcarbamothioyl)benzamide Chemical compound C=1C=CC=CC=1C(=O)NC(=S)NCC1=CC=CC=N1 AYYNLNBVTNAZEG-UHFFFAOYSA-N 0.000 description 1
- VWKDOEKIAWXRHQ-UHFFFAOYSA-N n-(pyridin-3-ylcarbamothioyl)benzamide Chemical compound C=1C=CC=CC=1C(=O)NC(=S)NC1=CC=CN=C1 VWKDOEKIAWXRHQ-UHFFFAOYSA-N 0.000 description 1
- DTQYAVJBZBATGD-UHFFFAOYSA-N n-(pyridin-3-ylmethylcarbamothioyl)hexanamide Chemical compound CCCCCC(=O)NC(=S)NCC1=CC=CN=C1 DTQYAVJBZBATGD-UHFFFAOYSA-N 0.000 description 1
- VMNCOVVGHFXZDJ-UHFFFAOYSA-N n-(pyrimidin-2-ylcarbamothioyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=NC=CC=N1 VMNCOVVGHFXZDJ-UHFFFAOYSA-N 0.000 description 1
- GHBDXIAKKZUHJS-UHFFFAOYSA-N n-[(1,5-dimethyl-3-oxo-2-phenylpyrazol-4-yl)carbamothioyl]benzamide Chemical compound O=C1N(C=2C=CC=CC=2)N(C)C(C)=C1NC(=S)NC(=O)C1=CC=CC=C1 GHBDXIAKKZUHJS-UHFFFAOYSA-N 0.000 description 1
- KZOAAJFQRCGRND-UHFFFAOYSA-N n-[(2,3-dichlorophenyl)carbamothioyl]-2-methylfuran-3-carboxamide Chemical compound O1C=CC(C(=O)NC(=S)NC=2C(=C(Cl)C=CC=2)Cl)=C1C KZOAAJFQRCGRND-UHFFFAOYSA-N 0.000 description 1
- DTALVJDYKHSJNI-UHFFFAOYSA-N n-[(2,3-dimethylphenyl)carbamothioyl]-3-phenylpropanamide Chemical compound CC1=CC=CC(NC(=S)NC(=O)CCC=2C=CC=CC=2)=C1C DTALVJDYKHSJNI-UHFFFAOYSA-N 0.000 description 1
- YHXYWEFRWVSTRI-UHFFFAOYSA-N n-[(2,4,6-trimethylphenyl)carbamothioyl]benzamide Chemical compound CC1=CC(C)=CC(C)=C1NC(=S)NC(=O)C1=CC=CC=C1 YHXYWEFRWVSTRI-UHFFFAOYSA-N 0.000 description 1
- AGXGQDJYLQDXQO-UHFFFAOYSA-N n-[(2,4-dichlorophenyl)carbamothioyl]-2-methylbenzamide Chemical compound CC1=CC=CC=C1C(=O)NC(=S)NC1=CC=C(Cl)C=C1Cl AGXGQDJYLQDXQO-UHFFFAOYSA-N 0.000 description 1
- WHLKULVCHONIGR-UHFFFAOYSA-N n-[(2,4-difluorophenyl)carbamothioyl]-2-methylbenzamide Chemical compound CC1=CC=CC=C1C(=O)NC(=S)NC1=CC=C(F)C=C1F WHLKULVCHONIGR-UHFFFAOYSA-N 0.000 description 1
- OGBBSOKGCOEBLQ-UHFFFAOYSA-N n-[(2,4-dimethylphenyl)carbamothioyl]-2-methylbenzamide Chemical compound CC1=CC(C)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1C OGBBSOKGCOEBLQ-UHFFFAOYSA-N 0.000 description 1
- FWBKDNZKHPYYIE-UHFFFAOYSA-N n-[(2,4-dimethylphenyl)carbamothioyl]-3-methylfuran-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C(=CC(C)=CC=2)C)=C1C FWBKDNZKHPYYIE-UHFFFAOYSA-N 0.000 description 1
- HXJSPFQECCKHOC-UHFFFAOYSA-N n-[(2,4-dimethylphenyl)carbamothioyl]-4-methylbenzamide Chemical compound C1=CC(C)=CC=C1C(=O)NC(=S)NC1=CC=C(C)C=C1C HXJSPFQECCKHOC-UHFFFAOYSA-N 0.000 description 1
- XMDUBTVENIIYAE-UHFFFAOYSA-N n-[(2,4-dimethylphenyl)carbamothioyl]furan-3-carboxamide Chemical compound CC1=CC(C)=CC=C1NC(=S)NC(=O)C1=COC=C1 XMDUBTVENIIYAE-UHFFFAOYSA-N 0.000 description 1
- PTDCJXPLLPSCQH-UHFFFAOYSA-N n-[(2,4-dioxo-1h-pyrimidin-5-yl)carbamothioyl]-4-methylbenzamide Chemical compound C1=CC(C)=CC=C1C(=O)NC(=S)NC1=CNC(=O)NC1=O PTDCJXPLLPSCQH-UHFFFAOYSA-N 0.000 description 1
- VDUYVDVXIYNSHE-UHFFFAOYSA-N n-[(2,5-dichlorophenyl)carbamothioyl]-2-phenoxypropanamide Chemical compound C=1C(Cl)=CC=C(Cl)C=1NC(=S)NC(=O)C(C)OC1=CC=CC=C1 VDUYVDVXIYNSHE-UHFFFAOYSA-N 0.000 description 1
- OMZLWMZOZZFLQI-UHFFFAOYSA-N n-[(2,5-dichlorophenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC(Cl)=CC=C1Cl OMZLWMZOZZFLQI-UHFFFAOYSA-N 0.000 description 1
- AFGVXSQAYKERLY-UHFFFAOYSA-N n-[(2,5-dimethoxyphenyl)carbamothioyl]-3-nitrobenzamide Chemical compound COC1=CC=C(OC)C(NC(=S)NC(=O)C=2C=C(C=CC=2)[N+]([O-])=O)=C1 AFGVXSQAYKERLY-UHFFFAOYSA-N 0.000 description 1
- CTNBRWQQGPHASM-UHFFFAOYSA-N n-[(2,5-dimethoxyphenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC(OC)=CC=C1OC CTNBRWQQGPHASM-UHFFFAOYSA-N 0.000 description 1
- PEBZVGOXWUGFCP-UHFFFAOYSA-N n-[(2,6-dichlorophenyl)carbamothioyl]-5-methylfuran-2-carboxamide Chemical compound O1C(C)=CC=C1C(=O)NC(=S)NC1=C(Cl)C=CC=C1Cl PEBZVGOXWUGFCP-UHFFFAOYSA-N 0.000 description 1
- VNMIXZLSPNJOGL-UHFFFAOYSA-N n-[(2,6-dichlorophenyl)carbamothioyl]benzamide Chemical compound ClC1=CC=CC(Cl)=C1NC(=S)NC(=O)C1=CC=CC=C1 VNMIXZLSPNJOGL-UHFFFAOYSA-N 0.000 description 1
- YCXISBLXDOZWST-UHFFFAOYSA-N n-[(2,6-dichlorophenyl)carbamothioyl]furan-3-carboxamide Chemical compound ClC1=CC=CC(Cl)=C1NC(=S)NC(=O)C1=COC=C1 YCXISBLXDOZWST-UHFFFAOYSA-N 0.000 description 1
- CKZLFTBGEWEPAP-UHFFFAOYSA-N n-[(2-chloro-5-nitrophenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC([N+]([O-])=O)=CC=C1Cl CKZLFTBGEWEPAP-UHFFFAOYSA-N 0.000 description 1
- XMAAUITXMKFGNA-UHFFFAOYSA-N n-[(2-chlorophenyl)carbamothioyl]benzamide Chemical compound ClC1=CC=CC=C1NC(=S)NC(=O)C1=CC=CC=C1 XMAAUITXMKFGNA-UHFFFAOYSA-N 0.000 description 1
- JKCRGVNAYIKKQS-UHFFFAOYSA-N n-[(2-chlorophenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=CC=C1Cl JKCRGVNAYIKKQS-UHFFFAOYSA-N 0.000 description 1
- OICGSNJNDYLOSO-UHFFFAOYSA-N n-[(2-chlorophenyl)methylcarbamothioyl]benzamide Chemical compound ClC1=CC=CC=C1CNC(=S)NC(=O)C1=CC=CC=C1 OICGSNJNDYLOSO-UHFFFAOYSA-N 0.000 description 1
- ZUNUEAHFMSKWHP-UHFFFAOYSA-N n-[(2-ethoxyphenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=CC=C1OCC ZUNUEAHFMSKWHP-UHFFFAOYSA-N 0.000 description 1
- WPROYJLAPYDIFE-UHFFFAOYSA-N n-[(2-fluorophenyl)carbamothioyl]-2-methylfuran-3-carboxamide Chemical compound O1C=CC(C(=O)NC(=S)NC=2C(=CC=CC=2)F)=C1C WPROYJLAPYDIFE-UHFFFAOYSA-N 0.000 description 1
- AQRCDOQDDBGXIU-UHFFFAOYSA-N n-[(2-fluorophenyl)carbamothioyl]-3-methylfuran-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C(=CC=CC=2)F)=C1C AQRCDOQDDBGXIU-UHFFFAOYSA-N 0.000 description 1
- YGRFDDLNTPTJAE-UHFFFAOYSA-N n-[(2-fluorophenyl)carbamothioyl]-5-methylfuran-2-carboxamide Chemical compound O1C(C)=CC=C1C(=O)NC(=S)NC1=CC=CC=C1F YGRFDDLNTPTJAE-UHFFFAOYSA-N 0.000 description 1
- NNACWBJTYFNZCZ-UHFFFAOYSA-N n-[(2-methoxy-4-nitrophenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=C([N+]([O-])=O)C=C1OC NNACWBJTYFNZCZ-UHFFFAOYSA-N 0.000 description 1
- JOIFWIJNENXQBY-UHFFFAOYSA-N n-[(2-methyl-4-nitrophenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=C([N+]([O-])=O)C=C1C JOIFWIJNENXQBY-UHFFFAOYSA-N 0.000 description 1
- XFIAIUAJRQOTAK-UHFFFAOYSA-N n-[(2-methyl-5-nitrophenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC([N+]([O-])=O)=CC=C1C XFIAIUAJRQOTAK-UHFFFAOYSA-N 0.000 description 1
- FCKGXEVHAIHNPA-UHFFFAOYSA-N n-[(2-nitrophenyl)carbamothioyl]benzamide Chemical compound [O-][N+](=O)C1=CC=CC=C1NC(=S)NC(=O)C1=CC=CC=C1 FCKGXEVHAIHNPA-UHFFFAOYSA-N 0.000 description 1
- XAAOMDKAYBKVAU-UHFFFAOYSA-N n-[(3,4-dichlorophenyl)carbamothioyl]-3,5-dinitrobenzamide Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC(C(=O)NC(=S)NC=2C=C(Cl)C(Cl)=CC=2)=C1 XAAOMDKAYBKVAU-UHFFFAOYSA-N 0.000 description 1
- VYOCYTLSSGROFR-UHFFFAOYSA-N n-[(3,4-dichlorophenyl)carbamothioyl]-3-methylfuran-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C=C(Cl)C(Cl)=CC=2)=C1C VYOCYTLSSGROFR-UHFFFAOYSA-N 0.000 description 1
- AAWMBROGCMAZMI-UHFFFAOYSA-N n-[(3,4-dichlorophenyl)carbamothioyl]-5-methylfuran-2-carboxamide Chemical compound O1C(C)=CC=C1C(=O)NC(=S)NC1=CC=C(Cl)C(Cl)=C1 AAWMBROGCMAZMI-UHFFFAOYSA-N 0.000 description 1
- YJEFQXFNNTUMQA-UHFFFAOYSA-N n-[(3,5-dibromopyridin-2-yl)carbamothioyl]-4-methylbenzamide Chemical compound C1=CC(C)=CC=C1C(=O)NC(=S)NC1=NC=C(Br)C=C1Br YJEFQXFNNTUMQA-UHFFFAOYSA-N 0.000 description 1
- JWKVNNJAPNWVEU-UHFFFAOYSA-N n-[(3,5-dibromopyridin-2-yl)carbamothioyl]thiophene-2-carboxamide Chemical compound BrC1=CC(Br)=CN=C1NC(=S)NC(=O)C1=CC=CS1 JWKVNNJAPNWVEU-UHFFFAOYSA-N 0.000 description 1
- RDUQJXKEOGTRAT-UHFFFAOYSA-N n-[(3-bromophenyl)carbamothioyl]naphthalene-1-carboxamide Chemical compound BrC1=CC=CC(NC(=S)NC(=O)C=2C3=CC=CC=C3C=CC=2)=C1 RDUQJXKEOGTRAT-UHFFFAOYSA-N 0.000 description 1
- DRAXNORTYURXSF-UHFFFAOYSA-N n-[(3-chloro-2-methylphenyl)carbamothioyl]-3,4,5-trimethoxybenzamide Chemical compound COC1=C(OC)C(OC)=CC(C(=O)NC(=S)NC=2C(=C(Cl)C=CC=2)C)=C1 DRAXNORTYURXSF-UHFFFAOYSA-N 0.000 description 1
- SUHMDRIZCDMZHB-UHFFFAOYSA-N n-[(3-chloro-2-methylphenyl)carbamothioyl]-4-fluorobenzamide Chemical compound CC1=C(Cl)C=CC=C1NC(=S)NC(=O)C1=CC=C(F)C=C1 SUHMDRIZCDMZHB-UHFFFAOYSA-N 0.000 description 1
- BYZKEODPNSTKBB-UHFFFAOYSA-N n-[(3-chlorophenyl)carbamothioyl]-2-fluorobenzamide Chemical compound FC1=CC=CC=C1C(=O)NC(=S)NC1=CC=CC(Cl)=C1 BYZKEODPNSTKBB-UHFFFAOYSA-N 0.000 description 1
- FNOYERCYLBXUHS-UHFFFAOYSA-N n-[(3-chlorophenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=CC(Cl)=C1 FNOYERCYLBXUHS-UHFFFAOYSA-N 0.000 description 1
- CNSGTWZSUDOORU-UHFFFAOYSA-N n-[(3-fluorophenyl)carbamothioyl]-3-nitrobenzamide Chemical compound [O-][N+](=O)C1=CC=CC(C(=O)NC(=S)NC=2C=C(F)C=CC=2)=C1 CNSGTWZSUDOORU-UHFFFAOYSA-N 0.000 description 1
- CAKOTOAHXFYCPA-UHFFFAOYSA-N n-[(3-methoxyphenyl)carbamothioyl]-2-methylbenzamide Chemical compound COC1=CC=CC(NC(=S)NC(=O)C=2C(=CC=CC=2)C)=C1 CAKOTOAHXFYCPA-UHFFFAOYSA-N 0.000 description 1
- HPZAQXVYVSRDGE-UHFFFAOYSA-N n-[(3-methoxyphenyl)carbamothioyl]naphthalene-1-carboxamide Chemical compound COC1=CC=CC(NC(=S)NC(=O)C=2C3=CC=CC=C3C=CC=2)=C1 HPZAQXVYVSRDGE-UHFFFAOYSA-N 0.000 description 1
- KECQWDNRDLXQKJ-UHFFFAOYSA-N n-[(3-methylphenyl)carbamothioyl]benzamide Chemical compound CC1=CC=CC(NC(=S)NC(=O)C=2C=CC=CC=2)=C1 KECQWDNRDLXQKJ-UHFFFAOYSA-N 0.000 description 1
- AKGAAPZENNXCLP-UHFFFAOYSA-N n-[(3-nitrophenyl)carbamothioyl]-3-phenylprop-2-enamide Chemical compound [O-][N+](=O)C1=CC=CC(NC(=S)NC(=O)C=CC=2C=CC=CC=2)=C1 AKGAAPZENNXCLP-UHFFFAOYSA-N 0.000 description 1
- ZMPXOIHAJRZQCE-UHFFFAOYSA-N n-[(3-nitrophenyl)carbamothioyl]naphthalene-2-carboxamide Chemical compound [O-][N+](=O)C1=CC=CC(NC(=S)NC(=O)C=2C=C3C=CC=CC3=CC=2)=C1 ZMPXOIHAJRZQCE-UHFFFAOYSA-N 0.000 description 1
- QGYAKSXPQCXZJN-UHFFFAOYSA-N n-[(4-acetamidophenyl)carbamothioyl]-2-phenoxyacetamide Chemical compound C1=CC(NC(=O)C)=CC=C1NC(=S)NC(=O)COC1=CC=CC=C1 QGYAKSXPQCXZJN-UHFFFAOYSA-N 0.000 description 1
- RUOBNTZHBICMEG-UHFFFAOYSA-N n-[(4-bromophenyl)carbamothioyl]-2,4-dichlorobenzamide Chemical compound ClC1=CC(Cl)=CC=C1C(=O)NC(=S)NC1=CC=C(Br)C=C1 RUOBNTZHBICMEG-UHFFFAOYSA-N 0.000 description 1
- ZBUMJPSTTUAHNC-UHFFFAOYSA-N n-[(4-bromophenyl)carbamothioyl]furan-3-carboxamide Chemical compound C1=CC(Br)=CC=C1NC(=S)NC(=O)C1=COC=C1 ZBUMJPSTTUAHNC-UHFFFAOYSA-N 0.000 description 1
- NVTNKRNENPWVBJ-UHFFFAOYSA-N n-[(4-chloro-2-methylphenyl)carbamothioyl]-2-methyl-3-phenylprop-2-enamide Chemical compound C=1C=C(Cl)C=C(C)C=1NC(=S)NC(=O)C(C)=CC1=CC=CC=C1 NVTNKRNENPWVBJ-UHFFFAOYSA-N 0.000 description 1
- KCQSSVAVSAGUTG-UHFFFAOYSA-N n-[(4-chlorophenyl)carbamothioyl]-2-methylfuran-3-carboxamide Chemical compound O1C=CC(C(=O)NC(=S)NC=2C=CC(Cl)=CC=2)=C1C KCQSSVAVSAGUTG-UHFFFAOYSA-N 0.000 description 1
- SPPIVJQNUMAIOG-UHFFFAOYSA-N n-[(4-chlorophenyl)carbamothioyl]-3-methylfuran-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C=CC(Cl)=CC=2)=C1C SPPIVJQNUMAIOG-UHFFFAOYSA-N 0.000 description 1
- GYKVYASPZLYFRG-UHFFFAOYSA-N n-[(4-chlorophenyl)carbamothioyl]-4-nitrobenzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)NC(=S)NC1=CC=C(Cl)C=C1 GYKVYASPZLYFRG-UHFFFAOYSA-N 0.000 description 1
- IZEIGTLVMJBUQC-UHFFFAOYSA-N n-[(4-chlorophenyl)carbamothioyl]benzamide Chemical compound C1=CC(Cl)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1 IZEIGTLVMJBUQC-UHFFFAOYSA-N 0.000 description 1
- PDPPVIICILSBPL-UHFFFAOYSA-N n-[(4-chlorophenyl)carbamothioyl]furan-2-carboxamide Chemical compound C1=CC(Cl)=CC=C1NC(=S)NC(=O)C1=CC=CO1 PDPPVIICILSBPL-UHFFFAOYSA-N 0.000 description 1
- ZGKFZHFFVYHYLH-UHFFFAOYSA-N n-[(4-chlorophenyl)carbamothioyl]naphthalene-1-carboxamide Chemical compound C1=CC(Cl)=CC=C1NC(=S)NC(=O)C1=CC=CC2=CC=CC=C12 ZGKFZHFFVYHYLH-UHFFFAOYSA-N 0.000 description 1
- PZPADESDNLWICR-UHFFFAOYSA-N n-[(4-ethoxyphenyl)carbamothioyl]-2-fluorobenzamide Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1F PZPADESDNLWICR-UHFFFAOYSA-N 0.000 description 1
- OUIIOMUEXIWQHW-UHFFFAOYSA-N n-[(4-ethoxyphenyl)carbamothioyl]-3-nitrobenzamide Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC(=O)C1=CC=CC([N+]([O-])=O)=C1 OUIIOMUEXIWQHW-UHFFFAOYSA-N 0.000 description 1
- YPQNTCDANNKRPC-UHFFFAOYSA-N n-[(4-ethoxyphenyl)carbamothioyl]naphthalene-1-carboxamide Chemical compound C1=CC(OCC)=CC=C1NC(=S)NC(=O)C1=CC=CC2=CC=CC=C12 YPQNTCDANNKRPC-UHFFFAOYSA-N 0.000 description 1
- VXLDMYBEUKPAGR-UHFFFAOYSA-N n-[(4-fluorophenyl)carbamothioyl]-2-methylfuran-3-carboxamide Chemical compound O1C=CC(C(=O)NC(=S)NC=2C=CC(F)=CC=2)=C1C VXLDMYBEUKPAGR-UHFFFAOYSA-N 0.000 description 1
- CCDCASANKGGEBH-UHFFFAOYSA-N n-[(4-fluorophenyl)carbamothioyl]-3-methylfuran-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C=CC(F)=CC=2)=C1C CCDCASANKGGEBH-UHFFFAOYSA-N 0.000 description 1
- SEIWNHDOJIGHBR-UHFFFAOYSA-N n-[(4-fluorophenyl)carbamothioyl]-3-nitrobenzamide Chemical compound [O-][N+](=O)C1=CC=CC(C(=O)NC(=S)NC=2C=CC(F)=CC=2)=C1 SEIWNHDOJIGHBR-UHFFFAOYSA-N 0.000 description 1
- FFVAHVHZSARXKQ-UHFFFAOYSA-N n-[(4-fluorophenyl)carbamothioyl]-4-methylbenzamide Chemical compound C1=CC(C)=CC=C1C(=O)NC(=S)NC1=CC=C(F)C=C1 FFVAHVHZSARXKQ-UHFFFAOYSA-N 0.000 description 1
- OFBLXEBHRFVRRX-UHFFFAOYSA-N n-[(4-fluorophenyl)carbamothioyl]-5-methylfuran-2-carboxamide Chemical compound O1C(C)=CC=C1C(=O)NC(=S)NC1=CC=C(F)C=C1 OFBLXEBHRFVRRX-UHFFFAOYSA-N 0.000 description 1
- KULMGSUBHSKTGH-UHFFFAOYSA-N n-[(4-hydroxyphenyl)carbamothioyl]-3-phenylprop-2-enamide Chemical compound C1=CC(O)=CC=C1NC(=S)NC(=O)C=CC1=CC=CC=C1 KULMGSUBHSKTGH-UHFFFAOYSA-N 0.000 description 1
- WFWDFLAMZLAXBB-UHFFFAOYSA-N n-[(4-iodophenyl)carbamothioyl]-2-methylfuran-3-carboxamide Chemical compound O1C=CC(C(=O)NC(=S)NC=2C=CC(I)=CC=2)=C1C WFWDFLAMZLAXBB-UHFFFAOYSA-N 0.000 description 1
- YFUJHEPEFFJWIN-UHFFFAOYSA-N n-[(4-iodophenyl)carbamothioyl]furan-3-carboxamide Chemical compound C1=CC(I)=CC=C1NC(=S)NC(=O)C1=COC=C1 YFUJHEPEFFJWIN-UHFFFAOYSA-N 0.000 description 1
- XCMQURIPKVDKQR-UHFFFAOYSA-N n-[(4-methoxy-2-nitrophenyl)carbamothioyl]benzamide Chemical compound [O-][N+](=O)C1=CC(OC)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1 XCMQURIPKVDKQR-UHFFFAOYSA-N 0.000 description 1
- SDHRBEVQJXGKOR-UHFFFAOYSA-N n-[(4-methoxyphenyl)carbamothioyl]-2-methylfuran-3-carboxamide Chemical compound C1=CC(OC)=CC=C1NC(=S)NC(=O)C1=C(C)OC=C1 SDHRBEVQJXGKOR-UHFFFAOYSA-N 0.000 description 1
- COBZRGLQABUNKW-UHFFFAOYSA-N n-[(4-methoxyphenyl)carbamothioyl]-4-methylbenzamide Chemical compound C1=CC(OC)=CC=C1NC(=S)NC(=O)C1=CC=C(C)C=C1 COBZRGLQABUNKW-UHFFFAOYSA-N 0.000 description 1
- UVNUMXHTNGBWFB-UHFFFAOYSA-N n-[(4-methoxyphenyl)carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=C(OC)C=C1 UVNUMXHTNGBWFB-UHFFFAOYSA-N 0.000 description 1
- KVOBWXQXTDADQH-UHFFFAOYSA-N n-[(4-methoxyphenyl)carbamothioyl]furan-3-carboxamide Chemical compound C1=CC(OC)=CC=C1NC(=S)NC(=O)C1=COC=C1 KVOBWXQXTDADQH-UHFFFAOYSA-N 0.000 description 1
- RALURLMXXCHCDQ-UHFFFAOYSA-N n-[(4-methylphenyl)carbamothioyl]furan-2-carboxamide Chemical compound C1=CC(C)=CC=C1NC(=S)NC(=O)C1=CC=CO1 RALURLMXXCHCDQ-UHFFFAOYSA-N 0.000 description 1
- AANIJPQAVWWBOE-UHFFFAOYSA-N n-[(4-morpholin-4-ylphenyl)carbamothioyl]-4-nitrobenzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)NC(=S)NC1=CC=C(N2CCOCC2)C=C1 AANIJPQAVWWBOE-UHFFFAOYSA-N 0.000 description 1
- ZSOPSVVEKQFKQA-UHFFFAOYSA-N n-[(4-morpholin-4-ylphenyl)carbamothioyl]benzamide Chemical compound C=1C=CC=CC=1C(=O)NC(=S)NC(C=C1)=CC=C1N1CCOCC1 ZSOPSVVEKQFKQA-UHFFFAOYSA-N 0.000 description 1
- BIAWGGYDQRXTRP-UHFFFAOYSA-N n-[(4-morpholin-4-ylphenyl)carbamothioyl]thiophene-2-carboxamide Chemical compound C=1C=CSC=1C(=O)NC(=S)NC(C=C1)=CC=C1N1CCOCC1 BIAWGGYDQRXTRP-UHFFFAOYSA-N 0.000 description 1
- YJMGBGAUFCFJGM-UHFFFAOYSA-N n-[(4-nitrophenyl)carbamothioyl]benzamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC(=S)NC(=O)C1=CC=CC=C1 YJMGBGAUFCFJGM-UHFFFAOYSA-N 0.000 description 1
- GTOWJDWFMVICEI-UHFFFAOYSA-N n-[(4-oxo-1,3-thiazol-2-yl)carbamothioyl]benzamide Chemical compound C=1C=CC=CC=1C(=O)NC(=S)NC1=NC(=O)CS1 GTOWJDWFMVICEI-UHFFFAOYSA-N 0.000 description 1
- YFBFCXHYATWCIU-UHFFFAOYSA-N n-[(4-tert-butylphenyl)carbamothioyl]-2-methylbenzamide Chemical compound CC1=CC=CC=C1C(=O)NC(=S)NC1=CC=C(C(C)(C)C)C=C1 YFBFCXHYATWCIU-UHFFFAOYSA-N 0.000 description 1
- AOZCGDKRKLQNPG-UHFFFAOYSA-N n-[(4-tert-butylphenyl)carbamothioyl]-2-methylfuran-3-carboxamide Chemical compound O1C=CC(C(=O)NC(=S)NC=2C=CC(=CC=2)C(C)(C)C)=C1C AOZCGDKRKLQNPG-UHFFFAOYSA-N 0.000 description 1
- XECGUVRAIAXZDK-UHFFFAOYSA-N n-[(4-tert-butylphenyl)carbamothioyl]-3-methylfuran-2-carboxamide Chemical compound C1=COC(C(=O)NC(=S)NC=2C=CC(=CC=2)C(C)(C)C)=C1C XECGUVRAIAXZDK-UHFFFAOYSA-N 0.000 description 1
- RVILHASRSVHLNV-UHFFFAOYSA-N n-[(4-tert-butylphenyl)carbamothioyl]furan-3-carboxamide Chemical compound C1=CC(C(C)(C)C)=CC=C1NC(=S)NC(=O)C1=COC=C1 RVILHASRSVHLNV-UHFFFAOYSA-N 0.000 description 1
- BQXASNGNIDHLFA-UHFFFAOYSA-N n-[(4-tert-butylphenyl)carbamothioyl]thiophene-2-carboxamide Chemical compound C1=CC(C(C)(C)C)=CC=C1NC(=S)NC(=O)C1=CC=CS1 BQXASNGNIDHLFA-UHFFFAOYSA-N 0.000 description 1
- AMPNOTFJOPBISS-UHFFFAOYSA-N n-[(5-methylpyridin-2-yl)carbamothioyl]furan-2-carboxamide Chemical compound N1=CC(C)=CC=C1NC(=S)NC(=O)C1=CC=CO1 AMPNOTFJOPBISS-UHFFFAOYSA-N 0.000 description 1
- KLAXKDMFUOHFON-UHFFFAOYSA-N n-[(6-methyl-4-oxo-1h-pyrimidin-2-yl)carbamothioyl]benzamide Chemical compound N1C(C)=CC(=O)N=C1NC(=S)NC(=O)C1=CC=CC=C1 KLAXKDMFUOHFON-UHFFFAOYSA-N 0.000 description 1
- XMFIVJIOTHURAJ-UHFFFAOYSA-N n-[2,2,2-trichloro-1-[(2,4-dichlorophenyl)carbamothioylamino]ethyl]formamide Chemical compound ClC1=CC=C(NC(=S)NC(NC=O)C(Cl)(Cl)Cl)C(Cl)=C1 XMFIVJIOTHURAJ-UHFFFAOYSA-N 0.000 description 1
- PGJJWPXICHBQCW-UHFFFAOYSA-N n-[2,2,2-trichloro-1-[(2,5-dichlorophenyl)carbamothioylamino]ethyl]formamide Chemical compound ClC1=CC=C(Cl)C(NC(=S)NC(NC=O)C(Cl)(Cl)Cl)=C1 PGJJWPXICHBQCW-UHFFFAOYSA-N 0.000 description 1
- HBOMOQRMLGFXNB-UHFFFAOYSA-N n-[2-(3,4-dimethoxyphenyl)ethylcarbamothioyl]benzamide Chemical compound C1=C(OC)C(OC)=CC=C1CCNC(=S)NC(=O)C1=CC=CC=C1 HBOMOQRMLGFXNB-UHFFFAOYSA-N 0.000 description 1
- BNJLVVVDIFJJSG-UHFFFAOYSA-N n-[3-(carbamothioylamino)phenyl]acetamide Chemical compound CC(=O)NC1=CC=CC(NC(N)=S)=C1 BNJLVVVDIFJJSG-UHFFFAOYSA-N 0.000 description 1
- WZUDNCUTQJSKJU-UHFFFAOYSA-N n-[4-(carbamothioylamino)phenyl]acetamide Chemical compound CC(=O)NC1=CC=C(NC(N)=S)C=C1 WZUDNCUTQJSKJU-UHFFFAOYSA-N 0.000 description 1
- DNOSJWLCWMYYMH-UHFFFAOYSA-N n-[4-(ethylcarbamothioylamino)phenyl]acetamide Chemical compound CCNC(=S)NC1=CC=C(NC(C)=O)C=C1 DNOSJWLCWMYYMH-UHFFFAOYSA-N 0.000 description 1
- OMOGRBVRZMBJGY-UHFFFAOYSA-N n-[[2-(1,1,2,2,3,3,3-heptafluoropropylsulfanyl)phenyl]carbamothioyl]thiophene-2-carboxamide Chemical compound FC(F)(F)C(F)(F)C(F)(F)SC1=CC=CC=C1NC(=S)NC(=O)C1=CC=CS1 OMOGRBVRZMBJGY-UHFFFAOYSA-N 0.000 description 1
- YTWPGYGRSKHYIV-UHFFFAOYSA-N n-[[2-(trifluoromethyl)phenyl]carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=CC=C1C(F)(F)F YTWPGYGRSKHYIV-UHFFFAOYSA-N 0.000 description 1
- PRDMIKJMVNACMH-UHFFFAOYSA-N n-[[2-(trifluoromethyl)phenyl]carbamothioyl]furan-2-carboxamide Chemical compound FC(F)(F)C1=CC=CC=C1NC(=S)NC(=O)C1=CC=CO1 PRDMIKJMVNACMH-UHFFFAOYSA-N 0.000 description 1
- XEJPDYBLACUINV-UHFFFAOYSA-N n-[[3,5-bis(trifluoromethoxy)phenyl]carbamothioyl]furan-3-carboxamide Chemical compound FC(F)(F)OC1=CC(OC(F)(F)F)=CC(NC(=S)NC(=O)C2=COC=C2)=C1 XEJPDYBLACUINV-UHFFFAOYSA-N 0.000 description 1
- FNXHNWLVEKCMSD-UHFFFAOYSA-N n-[[3-(1,1,2,2,3,3,3-heptafluoropropylsulfanyl)phenyl]carbamothioyl]thiophene-2-carboxamide Chemical compound FC(F)(F)C(F)(F)C(F)(F)SC1=CC=CC(NC(=S)NC(=O)C=2SC=CC=2)=C1 FNXHNWLVEKCMSD-UHFFFAOYSA-N 0.000 description 1
- KLFUYYZGYDCQSZ-UHFFFAOYSA-N n-[[4-(dimethylamino)phenyl]carbamothioyl]benzamide Chemical compound C1=CC(N(C)C)=CC=C1NC(=S)NC(=O)C1=CC=CC=C1 KLFUYYZGYDCQSZ-UHFFFAOYSA-N 0.000 description 1
- RNGQUOVGTHGRAH-UHFFFAOYSA-N n-[[4-(dimethylamino)phenyl]carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=C(N(C)C)C=C1 RNGQUOVGTHGRAH-UHFFFAOYSA-N 0.000 description 1
- ZVPPBAZRXYEYQQ-UHFFFAOYSA-N n-[[4-(trifluoromethoxy)phenyl]carbamothioyl]furan-2-carboxamide Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=S)NC(=O)C1=CC=CO1 ZVPPBAZRXYEYQQ-UHFFFAOYSA-N 0.000 description 1
- PFOBAINQIVZGKY-UHFFFAOYSA-N n-[[4-(trifluoromethyl)phenyl]carbamothioyl]furan-3-carboxamide Chemical compound C1=CC(C(F)(F)F)=CC=C1NC(=S)NC(=O)C1=COC=C1 PFOBAINQIVZGKY-UHFFFAOYSA-N 0.000 description 1
- MOMAGBVGEAHGDO-UHFFFAOYSA-N n-[[4-[acetyl(methyl)amino]phenyl]carbamothioyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(=S)NC1=CC=C(N(C)C(C)=O)C=C1 MOMAGBVGEAHGDO-UHFFFAOYSA-N 0.000 description 1
- XYAXWYSMSAAWKE-UHFFFAOYSA-N n-[anthracen-9-ylmethyl(methyl)carbamothioyl]benzamide Chemical compound C=12C=CC=CC2=CC2=CC=CC=C2C=1CN(C)C(=S)NC(=O)C1=CC=CC=C1 XYAXWYSMSAAWKE-UHFFFAOYSA-N 0.000 description 1
- POOZTTICQBYMAC-UHFFFAOYSA-N n-[bis(2-methylpropyl)carbamothioyl]benzamide Chemical compound CC(C)CN(CC(C)C)C(=S)NC(=O)C1=CC=CC=C1 POOZTTICQBYMAC-UHFFFAOYSA-N 0.000 description 1
- CTRPHZSFXIBKFI-UHFFFAOYSA-N n-[bis(prop-2-enyl)carbamothioyl]benzamide Chemical compound C=CCN(CC=C)C(=S)NC(=O)C1=CC=CC=C1 CTRPHZSFXIBKFI-UHFFFAOYSA-N 0.000 description 1
- HQWHWMJZCIBUFW-UHFFFAOYSA-N n-carbamothioyldodecanamide Chemical compound CCCCCCCCCCCC(=O)NC(N)=S HQWHWMJZCIBUFW-UHFFFAOYSA-N 0.000 description 1
- ILRILEJELKKXDV-UHFFFAOYSA-N n-carbamothioylhexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NC(N)=S ILRILEJELKKXDV-UHFFFAOYSA-N 0.000 description 1
- VYTYEDNCIFTZDH-UHFFFAOYSA-N n-phenylpiperidine-1-carbothioamide Chemical compound C1CCCCN1C(=S)NC1=CC=CC=C1 VYTYEDNCIFTZDH-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 231100000683 possible toxicity Toxicity 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- CFOJQUGXHMGMOT-UHFFFAOYSA-N pyridin-3-ylthiourea Chemical compound NC(=S)NC1=CC=CN=C1 CFOJQUGXHMGMOT-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- LZYDTZVMZCAOJQ-UHFFFAOYSA-N s-carbamimidoyl benzenecarbothioate Chemical compound NC(=N)SC(=O)C1=CC=CC=C1 LZYDTZVMZCAOJQ-UHFFFAOYSA-N 0.000 description 1
- VFIZBHJTOHUOEK-UHFFFAOYSA-N s-ethylisothiourea Chemical compound CCSC(N)=N VFIZBHJTOHUOEK-UHFFFAOYSA-N 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 230000021317 sensory perception Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- CSOJECDGWHHWRS-UHFFFAOYSA-N tert-butyl n-[(2-methylpropan-2-yl)oxycarbonylcarbamothioyl]carbamate Chemical compound CC(C)(C)OC(=O)NC(=S)NC(=O)OC(C)(C)C CSOJECDGWHHWRS-UHFFFAOYSA-N 0.000 description 1
- UQJXXWHAJKRDKY-UHFFFAOYSA-N tert-butyl n-[[(2-methylpropan-2-yl)oxycarbonylamino]-methylsulfanylmethylidene]carbamate Chemical compound CC(C)(C)OC(=O)NC(SC)=NC(=O)OC(C)(C)C UQJXXWHAJKRDKY-UHFFFAOYSA-N 0.000 description 1
- JKXQTODLIZBUDE-UHFFFAOYSA-N tert-butyl n-carbamothioylcarbamate Chemical compound CC(C)(C)OC(=O)NC(N)=S JKXQTODLIZBUDE-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003513 tertiary aromatic amines Chemical class 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 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
- C08F4/00—Polymerisation catalysts
- C08F4/40—Redox systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/20—Protective coatings for natural or artificial teeth, e.g. sealings, dye coatings or varnish
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/30—Compositions for temporarily or permanently fixing teeth or palates, e.g. primers for dental adhesives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/50—Preparations specially adapted for dental root treatment
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/887—Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/891—Compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- A61K6/893—Polyurethanes
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dental Preparations (AREA)
- Polymerization Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Dental Tools And Instruments Or Auxiliary Dental Instruments (AREA)
Abstract
【解決手段】(a)第3級炭素と結合している1個または複数個のヒドロペルオキシド基を有するヒドロペルオキシド化合物;(b)チオ尿素誘導体;および(c)促進剤として、調製物中で溶解性の銅化合物を有し、好ましくはアミン不含である、二成分開始剤系により解決される。これは、特に重合可能な歯科用組成物に適している。
【選択図】なし
Description
1.ベンゾイルペルオキシド/tert−芳香族アミン:ジベンゾイルペルオキシドは、アミン開始可能なペルオキシドの中で、最も高い熱安定性を示す。それにもかかわらず、調製物の持続的な加熱は、すぐに生じる自然硬化を招く。歯科的使用のための欠点は、さらに、ゆっくり生じるアミンの酸化であり、この場合、これは、黄褐色への変色を招き、審美的妨げとなる。たとえば接着剤中で必要不可欠な酸性環境下においては、アミンは、酸−塩基反応中ですぐにプロトン化され、それにより不活性化される。このような条件下では、二成分系を使用することはできない。
2.バルビツール酸誘導体:
歯科的使用においてバルビツール酸誘導体は好ましく使用され、それというのも、強い後変色が生じないためである。第2の成分は、バルビツール酸の分解を触媒する銅イオンおよび塩化物イオンを含有する。さらに、アミンを含有しないことから、系を酸性条件下で使用することができる。低い熱安定性の理由から、生成物は、常に冷所で貯蔵しなければならない。開始剤成分は、反応性の架橋性成分を含有するものではあってはならず、それというのも、自発的に硬化が生じるためである。
3.クメンヒドロペルオキシド/アセチルチオ尿素:歯内療法的シーリング系が、US2003/0134933(Pentron)に記載されている。これは、多量(1〜10%)のクメンヒドロペルオキシドおよびアセチルチオ尿素を含み、かつ、JP58219281A(Mitsubishi)の接着剤の記載を参考にすることもできる。ここでは、従来の系に対して極めて高い熱安定性が記載されている。しかしながら組成物の調整は、低い濃度範囲では、不適切なゆっくりとした硬化速度を示す。記載の下限(それぞれ1%)においては、全く重合が生じることはない。
4.クメンヒドロペルオキシド/促進剤:DE19501933(Henkel)による接着剤は、開始剤としてヒドロペルオキシドおよび促進剤として以下の化合物を含有する:スルフィミド、ヒドラジン誘導体、tert.−アミンおよび銅塩または銅錯体。付加的に、架橋を促進するための乾燥剤を含有していてもよい。個々の組成物中の高い反応性が達成されるが、但し、これらは、金属塩により強力に着色され、強い黄味を帯びるか、あるいは、不十分な貯蔵安定性を示す。
5.過酸化物/金属化合物:熱安定化性過酸化物を有する重合可能な組成物は、DE69621500(Dentsply)に記載されている。重合可能な系は、クメンヒドロペルオキシドの他に、チオ尿素複合体としてさらに金属化合物を含有していてもよい。金属化合物として、特に銅化合物が記載されている。これは、さらに酸およびアミンを含有していなければならない。請求項において、特に粉体−液体系が記載されている。記載したように開始剤系は、酸含有環境下で、明らかな効果が示されているにもかかわらす、含有されるアミンが、このような生成物の典型的な変色を招きうる。
6.EP1479364A1では、アミン不含の二成分歯科用組成物が記載されており、この場合、この組成物は、チオ尿素−ヒドロペルオキシド開始剤系を包含するものである。
a)組成物は、極めて高い貯蔵安定性を有する二成分開始剤系を示す。これは後着色を示すことなく、かつ酸によって影響を受けることはない。銅含量を変更することによって、阻害時間は極めて可変に調整可能である。種々の組み合わせに対する多くの試験を実施し、かつそれぞれ阻害時間を測定した。クメンヒドロペルオキシド、アセチル−チオ尿素および銅塩の濃度は、可変である。2種の銅塩(アセチルアセトネート、ナフテネート)を試験したが、その際、反応性の差は観察されなかった。阻害時間は、酸性条件下で、リン酸エステル(2%、5%)、4−META(15%)およびアクリル酸(5%)の組み合わせによって測定された。すべての調製物の貯蔵安定性は、50℃で、3ヶ月までの期間に亘って観察した。銅含量の影響を、ポリマーの着色において測定する。着色安定性を試験した。
b)開始剤系は、すべてのラジカル重合可能な系に関して自在に調整可能である。医科または歯科用接着剤の製造に関して、極めて良好な貯蔵安定性および少ない変色傾向は、特に有利である。酸性成分を有する組み合わせ物のための可能性は、新規使用分野を開拓する(接着剤、自己粘着性調製物)。
c)ジベンゾイルペルオキシドおよび第3級芳香族アミンから成る通常の二成分系と比較して、貯蔵安定性の顕著な改善が示され、さらに酸性条件下で働き、かつ改善した色安定性を示す。
d)組成物が、レドックス系を記載し、かつ酸化剤としてのヒドロペルオキシドおよび還元剤としてのチオ尿素誘導体を、活性化された状態で含有する。このように記載された開始剤系は、すでに特許文献JP58219281、US2003/0134933、US2003/0166740およびEP1479364から公知である。
1−(1,1−ジオキソ−テトラヒドロ−チオフェン−3−イル)−1−メチル−3−フェニル−チオ尿素、
1−(1,2−ジフェニルエチル)−3−(2,4−キシリル)−2−チオ尿素、
1−(1,2−ジフェニルエチル)−3−(4−エトキシフェニル)−2−チオ尿素、
1−(1,2−ジフェニルエチル)−3−(o−トリル)−2−チオ尿素、
1−(1,2−ジフェニルエチル)−3−フェニル−2−チオ尿素、
1,1’−(3,3’−ジメチルビフェニル−4,4’−ジイル)ビス(3−(2−メチルプロピル)−2−チオ尿素、
1,1,3−トリフェニル−2−チオ尿素、
1,1’−(4,5−ジメチル−1,2−フェニレン)ビス(3−フェニル−2−チオ尿素)、
1−(1,5−DI−ME−3−オキソ−2−PH−2,3−ジヒドロ−1−H−ピラゾール−4−イル)−3−(2−メチル−アリル)チオ尿素、
1−(1,5−DI−ME−3−オキソ−2−PH−2,3−ジヒドロ−1−H−ピラゾール−4−イル)−3−(3−トリ−F−ME−PH)チオ尿素、
1−(1,5−ジメチル−3−オキソ−2−フェニル−2,3−ジヒドロ−1H−ピラゾール−4−イル)−3−フェニルチオ尿素、
1,1−ビス−(2−ヒドロキシ−エチル)−3−フェニル−チオ尿素、
1,1−ジアリル−3−(3−クロロ−ベンゾ(B)チオフェン−2−カルボニル)−チオ尿素、
1,1−ジアリル−3−(4−ニトロフェニル)−2−チオ尿素、
1,1−ジアリル−3−フェニル−2−チオ尿素、
1,1−ジベンジル−3−(2,4−ジクロロ−ベンゾイル)−チオ尿素、
1,1−ジベンジル−3−(2−(トリフルオロメチル)フェニル)−2−フェニル−チオ尿素、
1,1−ベンジル−3−フェニル−2−チオ尿素、
1,1−ジブチル−3−フェニル−2−チオ尿素、
1,1−ジエチル−3−フェニル−2−チオ尿素、
1,1−ジイソブチル−3−フェニル−2−チオ尿素。
1,1−ジメチル−3−(2,6−キシリル)−2−チオ尿素、
1,1−ジメチル−3−(2−メトキシフェニル)−2−チオ尿素、
1,1−ジメチル−3−(3,4−キシリル)−2−チオ尿素、
1,1−ジメチル−3−(4−エトキシフェニル)−2−チオ尿素、
1,1−ジメチル−3−(4−メトキシフェニル)−2−チオ尿素、
1,1−ジメチル−3−(α−(メチルイミノ)ベンジル)−2−チオ尿素、
1,1−ジメチル−3−(m−トリル)−2−チオ尿素、
1,1−ジメチル−3−(o−トリル)−2−チオ尿素、
1,1−ジメチル−3−(p−トリル)−2−チオ尿素、
1,1−ジメチル−3−フェニル−2−チオ尿素、
1,1−ジプロピル−3−フェニル−2−チオ尿素、
1−(1−エチル−3−ピペリジニル)−3−フェニル−2−チオ尿素、
1−(1−ナフチル)−2−チオ尿素、
1−(1−ナフチル)−3−(2−フェノキシプロピオニル)−2−チオ尿素、
1,1−ペンタメチレン−3−フェニル−2−チオ尿素、
1−(2,2−ジメチル−プロピル)−3−(2−フルオロ−フェニル)−チオ尿素、
1−(2−(2−ヒドロキシ−エトキシ)エチル)−3−フェニル−チオ尿素、
1−(2,4,6−トリブロモフェニル)−2−チオ尿素、
1−(2,4−ジクロロベンゾイル)−3−(1−ナフチル)−2−チオ尿素、
1−(2,4−ジクロロベンゾイル)−3−(7−ヒドロキシ−1−ナフチル)−2−チオ尿素、
1−(2,4−ジクロロフェニル)−2−チオ尿素、
1−(2,4−ジフルオロフェニル)−3−(2−フルオロフェニル)−2−チオ尿素、
1−(2,4−ジフルオロフェニル)−3−(4−フェノキシフェニル)−2−チオ尿素。
1−(2,5−ジクロロフェニル)−3−(2−フェノキシプロピオニル)−2−チオ尿素、
1−(2,5−ジクロロフェニル)−3−ドデカノイル−2−チオ尿素、
1−(2,5−ジクロロフェニル)−3−フェニル−2−チオ尿素、
1−(2,5−ジメトキシフェニル)−3−(3−ニトロベンゾイル)−2−チオ尿素、
1−(2,5−ジメトキシフェニル)−3−ドデカノイル−2−チオ尿素、
1−(2,5−ジメトキシフェニル)−3−メチル−2−チオ尿素、
1−(2,5−ジメトキシフェニル)−3−フェニル−2−チオ尿素、
1−(2,5−ジメトキシフェニル)−3−プロピル−2−チオ尿素、
1−(2,5−ジメチルモルホリノ)−3−フェニル−2−チオ尿素、
1−(2,6−ジエチルフェニル)−3−(4−ヒドロキシフェニル)−2−チオ尿素、
1−(2,6−キシリル)−2−チオ尿素、
1−(2−ブロモ−4−メチル−フェニル)−3−フェニル−チオ尿素、
1−(2−ブロモフェニル)−2−チオ尿素、
1−(2−カルボキシフェニル)−3−フェニル−2−チオ尿素、
1−(2−クロロ−4−メトキシフェニル)−3−シクロヘキシル−2−チオ尿素
1−(2−クロロ−4−ニトロフェニル)−3−(3,4−ジクロロベンゾイル)−2−チオ尿素、
1−(2−クロロ−4−ニトロフェニル)−3−エチル−2−チオ尿素、
1−(2−クロロ−5−ニトロフェニル)−3−ドデカノイル−2−チオ尿素、
1−(2−クロロベンゾイル)−3−(2,4−ジフルオロフェニル)−2−チオ尿素、
1−(2−クロロベンゾイル)−3−(2,4−ジメトキシフェニル)−2−チオ尿素、
1−(2−クロロベンゾイル)−3−(2−フルオロフェニル)−2−チオ尿素。
1−(2−クロロベンゾイル)−3−(3,4−ジクロロフェニル)−2−チオ尿素、
1−(2−クロロベンゾイル)−3−(3−クロロフェニル)−2−チオ尿素、
1−(2−クロロベンゾイル)−3−(4−ニトロフェニル)−2−チオ尿素、
1−(2−クロロベンゾイル)−3−(5−クロロ−2−メトキシフェニル)−2−チオ尿素、
1−(2−クロロベンジル)−3−シクロヘキシル−1−メチル−2−チオ尿素、
1−(2−クロロフェニル)−3−(2,4−ジクロロベンゾイル)−2−チオ尿素、
1−(2−クロロフェニル)−3−ドデカノイル−2−チオ尿素、
1−(2−クロロフェニル)−3−フェニル−2−チオ尿素、
1−(2−エチルフェニル)−3−メチル−2−チオ尿素、
1−(2−フルオロベンゾイル)−3−(4−エトキシフェニル)−2−チオ尿素、
1−(2−フルオロベンゾイル)−3−(4−フルオロフェニル)−2−チオ尿素、
1−(2−(ヘキサデシルチオ)フェニル)−2−チオ尿素、
1−(2−ヒドロキシ−1−フェニル−エチル)−3−フェニル−チオ尿素、
1−(2−ヒドロキシ−シクロヘキシル)−3−フェニル−2−チオ尿素、
1−(2−ヒドロキシエチル)−3−(2,4−キシリル)−2−チオ尿素、
1−(2−ヒドロキシエチル)−3−フェニル−2−チオ尿素、
1−(2−メトキシ−5−メチルフェニル)−1−メチル−3−(2−ナフチル)−2−チオ尿素、
1−(2−メトキシ−フェニル)−3−(2−メチルベンゾイル)フ−チオ尿素、
1−(2−メトキシフェニル)−2−チオ尿素、
1−(2−メトキシフェニル)−2−チオ尿素、
1−(2−メチル−2−モルホリン−4−イルプロピル)−3−フェニル−チオ尿素。
1−(2−メチルアリル)−3−(6−(3−(2−メチルアリル)−チオウレイド)−ピリジン−2−イル)−チオ尿素、
1−(2−メチルベンゾイル)−3−p−トリル−チオ尿素、
1−(2−メチルベンゾイル)−3−フェニル−チオ尿素、
1−(2−メチルベンゾイル)−3−ピリミジン−2−イル−チオ尿素,
1−(2,5−モルホリノエチル)−3−フェニル−2−チオ尿素、
1−(2−ナフチル)−3−フェニル−2−チオ尿素、
1−(2−ニトロフェニル)−3−フェニル−2−チオ尿素、
1−(2−ピリジル)−3−(3,4−キシリル)−2−チオ尿素、
1−(2−ピリジル)−3−(o−トリル)−2−チオ尿素、
1−(3−(2−メルカプトエチル)−3H−ベンゾチオアゾール−2−イリデン)−2−ME−イソチオ尿素,ヨウ化水素化物
1−(3,4−ジブロモフェニル)−3−フェニル−2−チオ尿素、
1−(3,4−クロロベンゾイル)−3−(2,4−ジフルオロフェニル)−2−チオ尿素、
1−(3,4−ジクロロベンゾイル)−3−(2−フルオロフェニル)−2−チオ尿素、
1−(3,4−ジクロロベンゾイル)−3−(2−チアゾリル)−2−チオ尿素、
1−(3,4−ジクロロベンゾイル)−3−(3,4−ジクロロフェニル)−2−チオ尿素、
1−(3,4−ジクロロベンゾイル)−3−(4−エトキシフェニル)−2−チオ尿素、
1−(3,4−ジクロロベンゾイル)−3−(4−ニトロフェニル)−2−チオ尿素、
1−(3,4−ジクロロベンゾイル)−3−(4−スルファモイル)フェニル−2−チオ尿素、
1−(3,4−ジクロロフェニル)−2−チオ尿素、
1−(3,4−ジクロロフェニル)−3−(3,5−ジニトロベンゾイル)−2−チオ尿素。
1−(3,4−ジクロロフェニル)−3−(ジフェニルメチル)−2−チオ尿素、
1−(3,4−ジクロロフェニル)−3−フェニル−2−チオ尿素、
1−(3,4−ジメトキシベンジル)−3−フェニル−チオ尿素
1−(3,4−ジメトキシフェニル)−2−チオ尿素、
1−(3,5−ジクロロベンジル)−3−フェニル−2−チオ尿素、
1−(3,5−ジクロロフェニル)−2−チオ尿素、
1−(3−アセチルフェニル)−3−アリル−2−チオ尿素、
1−(3−アセチルフェニル)−3−エチル−2−チオ尿素
1,3−ビス(2,6−ジクロロフェニル)−2−チオ尿素、
1,3−ビス(2−クロロフェニル)−2−チオ尿素、
1,3−ビス(2−フルオロフェニル)−2−チオ尿素、
1,3−ビス(2−メトキシフェニル)−2−チオ尿素、
1,3−ビス(3−アセチルフェニル)−2−チオ尿素、
1,3−ビス(3−ブロモフェニル)−2−チオ尿素、
1,3−ビス(3−シアノフェニル)−2−チオ尿素、
1,3−ビス(3−ヨードフェニル)−2−チオ尿素、
1,3−ビス(3−メトキシフェニル)−2−チオ尿素、
1,3−ビス(3−ニトロフェニル)−2−チオ尿素、
1,3−ビス(3−ピリジルメチル)−2−チオ尿素、
1,3−ビス(4−ブロモフェニル)−2−チオ尿素、
1,3−ビス(4−クロロフェニル)−2−チオ尿素、
1,4−ビス(3−シアノフェニル)−2−チオ尿素。
1−(3−ブロモフェニル)−3−(2−メチルベンゾイル)−チオ尿素、
1−(3−ブロモフェニル)−3−(ナフタレン−1−カルボニル)−チオ尿素、
1−(3−ブロモベンゾイル)−3−(3−クロロフェニル)−2−チオ尿素、
1−(3−ブトキシプロピル)−3−フェニル−2−チオ尿素、
1−(3−カルボキシフェニル)−2−チオ尿素、
1−(3−クロロ−2−メチルフェニル)−3−(−3,4,5−トリメトキシベンゾイル)−チオ尿素、
1−(3−クロロ−2−メチルフェニル)−3−(−4−フルオロベンゾイル)−チオ尿素、
1−(3−クロロ−ベンゾ(B)チオフェン−2−カルボニル)−3−(4−ニトロフェニル)チオ尿素、
1−(3−クロロベンジル)−3−フェニル−2−チオ尿素、
1−(3−クロロフェニル)−2−チオ尿素、
1−(3−クロロフェニル)−3−(2−フルオロベンゾイル)−2−チオ尿素、
1−(3−クロロフェニル)−3−(3,4−ジクロロベンゾイル)−2−チオ尿素、
1−(3−クロロフェニル)−3−ドデカノイル−2−チオ尿素、
1−(3−クロロフェニル)−3−フェニル−2−チオ尿素、
1,3−ジ−o−トリル−2−チオ尿素
1,3−ジ−o−トリル−2−チオ尿素
1,3−ジ−p−トリル−2−チオ尿素、
1,3−ジ−t−ブチル−2−チオ尿素
1,3−ジアリル−2−チオ尿素、
1,3−ジベンジル−2−チオ尿素、
1−(3−(ジブチルアミノ)プロピル)−3−フェニル−2−チオ尿素。
1,3−ジデシル−2−チオ尿素、
1,3−ジドデシル−2−チオ尿素
1,3−ジフルルリル−2−チオ尿素、
1,3−ジヘプチル−2−チオ尿素、
1,3−ジヘキサデシル−2−チオ尿素、
1,3−ジヘキシル−2−チオ尿素、
1,3−ジイソプロピル−2−チオ尿素、
1,3−ジオクチル−2−チオ尿素、
1,3−ジプロピル−2−チオ尿素、
1,3−ジテトラデシル−2−チオ尿素、
1−(3−フルオロフェニル)−3−(3−ニトロベンゾイル)−2−チオ尿素、
1−(3−フルオロフェニル)−3−メチル−2−チオ尿素、
1−(3−ヒドロキシフェニル)−3−(4−ヒドロキシフェニル)−2−チオ尿素、
1−(3−ヒドロキシフェニル)−3−フェニル−2−チオ尿素、
1−(3−メトキシフェニル)−3−(2−メチルベンゾイル)−チオ尿素、
1−(3−メトキシフェニル)−3−(ナフタレン−1−カルボニル)−チオ尿素、
1−(3−メトキシプロピル)−2−チオ尿素、
1−(3−ニトロ−フェニル)−3−(3−フェニルアクリロイル)−チオ尿素、
1−(3−ニトロフェニル)−3−フェニル−2−チオ尿素、
1−(3−フェニルプロピオニル)−3−(2,3−キシリル)−2−チオ尿素、
1−(3−ピリジル)−2−チオ尿素、
1−(3−(トリフルオロメチル)フェニル)−2−チオ尿素、
1−(3−トリフルオロメチルフェニル)−3−(2,3,4−トリメトキシベンゾイル)−チオ尿素。
1−(4−アセタミドフェニル)−3−(2−ブテノイル)−2−チオ尿素、
1−(4−アセタミドフェニル)−3−(2−フェノキシアセチル)−2−チオ尿素、
1−(4−アセタミドフェニル)−3−エチル−2−チオ尿素、
1−(4−アセチルフェニル)−3−メチル−2−チオ尿素、
1−(4−ブロモ−フェニル)−3−(2,4−ジクロロベンゾイル)−チオ尿素、
1−(4−クロロ−2,5−ジメトキシフェニル)−3−(4−ニトロフェニル)−2−チオ尿素、
1−(4−クロロ−2,5−ジメトキシフェニル)−3−メチル−2−チオ尿素、
1−(4−クロロ−2−メチルフェニル)−3−(−2−メチル−3−フェニル−アクリロイル)−チオ尿素、
1−(4−クロロフェニル−2−メチルフェニル)−3−ドデカノイル−2−チオ尿素、
1−(4−クロロ−7−メトキシ−2−キノリル)−3−フェニル−2−チオ尿素、
1−(4−クロロ−フェニル)−3−(4−ニトロベンゾイル)−チオ尿素、
1−(4−クロロフェニル)−3−(ナフタレン−1−カルボニル)−チオ尿素、
1−(4−クロロベンジル)−3−メチル−3−フェニル−2−チオ尿素、
1−(4−クロロフェニル)−2−チオ尿素、
1−(4−クロロフェニル)−3−(2−ピリジル)−2−チオ尿素、
1−(4−クロロフェニル)−3−(4−ジエチルアミノ−o−トリル)−2−チオ尿素、
1−(4−クロロフェニル)−3−フェニル−2−チオ尿素、
1−(4−ジフルオロメトキシ−2−ホルミルフェニル)−3−(1,2,2−トリメチルプロピル)チオ尿素、
1−(4−ジフルオロメトキシフェニル)−3−(1,2,2−トリメチルプロピル)チオ尿素。
1−(4−(ジメチルアミノ)フェニル)−3−(4−ニトロフェニル)−2−チオ尿素、
1−(4−(ジメチルアミノ)フェニル)−3−ドデカノイル−2−チオ尿素、
1−(4−(ジメチルアミノ)フェニル)−3−(フェニル)−2−チオ尿素、
1−(4−エトキシカルボニル)−3−エチル−2−チオ尿素、
1−(4−エトキシフェニル)−3−(1−ナフチルカルボニル)−2−チオ尿素、
1−(4−エトキシフェニル)−3−(2−ピリジル)−2−チオ尿素、
1−(4−エトキシフェニル)−3−(3−ニトロベンゾイル)−2−チオ尿素、
1−(4−エトキシフェニル)−3−エチル−2−チオ尿素、
1−(4−エチルフェニル)−3−フェニル−2−チオ尿素、
1−(4−フルオロフェニル)−3−(2,4,6−トリメチルフェニル)−2−チオ尿素、
1−(4−フルオロフェニル)−3−(3−ニトロベンゾイル)−2−チオ尿素、
1−(4−(ヘキサデシルスルホニル)−フェニル)−2−チオ尿素、
1−(4−ヒドロキシフェニル)−3−プロピル−2−チオ尿素、
1−(4−ヨードフェニル)−3−(3−フェノキシプロピオニル)−2−チオ尿素、
1−(4−MEO−フェニル)−3−((4−MEO−フェニル)−(トルエン−4−スルホニルメチルイミノ)−メチル)−チオ尿素、
1−(4−メトキシベンジル)−3−フェニル−チオ尿素、
1−(4−メトキシ−フェニル)−3−(4−メチルベンゾイル)−チオ尿素、
1−(4−メトキシ−フェニル)−3−フェニル−チオ尿素、
1−(4−メトキシフェニル)−3−(2−ピリジル)−2−チオ尿素、
1−(4−メトキシフェニル)−3−(2−ピリジル)−2−チオ尿素。
1−(4−ニトロベンゾイル)−3−ピリジン−2−イルメチル−チオ尿素,
1−(4−ニトロフェニル)−2−チオ尿素、
1−(4−ニトロフェニル)−3−(3−(トルフルオロメチル)フェニル)−2−チオ尿素、
1−(4−ニトロフェニル)−3−フェニル−2−チオ尿素、
1−(4−ピリジルメチル)−3−(2,6−キシリル)−2−チオ尿素、
1−(4−t−ブチルフェニル)−2−チオ尿素、
1−(4−トリフルオロメトキシ−フェニル)−3−(1,2,2−トリメチルプロピル)チオ尿素、
1−(4−トリフルオロメチルスルファニル−フェニル)−3−(1,2,2−トリメチルプロピル)チオ尿素、
1−(5−アニリノ−1,2,4−チアジアゾール−3−イル)−3−フェニル−2−チオ尿素、
1−(5−ブロモ−3−メチル−ピリジン−2−イル)−3−フェニル−チオ尿素
1−(5−クロロ−2,4−ジメトキシフェニル)−3−(2,4−ジフルオロフェニル)−2−チオ尿素、
1−(5−クロロ−2,4−ジメトキシフェニル)−3−(2,5−ジフルオロフェニル)−2−チオ尿素、
1−(5−クロロ−2,4−ジメトキシフェニル)−3−(2−フルオロフェニル)−3−メチル−2−チオ尿素、
1−(5−クロロ−2,4−ジメトキシフェニル)−3−メチル−2−チオ尿素、
1−(5−クロロ−2−メトキシフェニル)−3−(3,4−ジクロロベンゾイル)−2−チオ尿素
1−(5−クロロ−2−メトキシフェニル)−3−フェニル−2−チオ尿素。
1−アセチル−3−フェニル−2−チオ尿素、
1−アリル−3−(1,2−ジフェニルエチル)−2−チオ尿素、
1−アリル−3−(1,5−ジメチル−3−オキソ−2−フェニル−2,3−ジヒドロ−1H−ピラゾール−4−イル)−チオ尿素
1−アリル−3−(1−ナフチル)−2−チオ尿素、
1−アリル−3−(1−ナフチルメチル)−2−チオ尿素、
1−アリル−3−(2−(1−ヒドロキシエチル)フェニル)−2−チオ尿素、
1−アリル−3−(2−エトキシフェニル)−2−チオ尿素、
1−アリル−3−(3−クロロフェニル−2−メチルフェニル)−2−チオ尿素、
1−アリル−3−(3−ヒドロキシフェニル)−2−チオ尿素、
1−アリル−3−(4−クロロベンジル)−2−チオ尿素、
1−アリル−3−(4−クロロフェニル)−2−チオ尿素、
1−アリル−4−(3−ヒドロキシフェニル)−2−チオ尿素、
1−アリル−3−(ジフェニルメチル)−2−チオ尿素、
1−アリル−3−モルホリン−4−イル−チオ尿素、
1−アリル−3−o−トリル−チオ尿素
1−アリル−3−オクタデシル−2−チオ尿素、
1−アリル−3−フェニル−2−チオ尿素、
1−(α−メチルベンジル)−3−(4−ピリジルメチル)−2−チオ尿素、
1−(α−メチルベンジル)−3−フェニルチオ尿素、
1−アミジノ−2−チオ尿素オキサレート、
1−アミジノ−3−(4−ブロモフェニル)−2−チオ尿素、
1−アミジノ−3−ベンゾイル−2−チオ尿素、
1−アミジノ−3−メチル−2−チオ尿素−p−トルエンスルホネート。
1−アミジノ−3−プロピル−2−チオ尿素、
1−アミジノ−3−プロピル−2−チオ尿素−p−トルエンスルホネート、
1−ベンゾチアゾール−2−イル−3−フェニル−チオ尿素、
1−ベンゾイル−3−(1,5−ジメチル−3−オキソ−2−フェニル−2,3−ジヒドロ−1H−ピラゾール−4−イル)−チオ尿素
1−ベンゾイル−3−(1,5−ジメチル−3−オキソ−2−フェニル−ピラゾリジン−4−イル)−チオ尿素
1−ベンゾイル−3−(2,4,6−トリメチル−フェニル)−チオ尿素、
1−ベンゾイル−3−(2,6−ジクロロフェニル)−2−チオ尿素、
1−ベンゾイル−3−(2−クロロ−ベンジル)−チオ尿素、
1−ベンゾイル−3−(2−クロロフェニル)−2−チオ尿素、
1−ベンゾイル−3−(3,4−ジメトキシフェネチル)−2−チオ尿素、
1−ベンゾイル−3−(4−ジメチルアミノ−フェニル)−チオ尿素、
1−ベンゾイル−3−(4−メトキシ−2−ニトロフェニル)−2−チオ尿素、
1−ベンゾイル−3−(4−モルホリン−4−イルフェニル)−チオ尿素、
1−ベンゾイル−3−(4−ニトロフェニル)−2−チオ尿素、
1−ベンゾイル−3−(4−オキソ−チアゾリジン−2−イリデン)−チオ尿素、
1−ベンゾイル−3−(α,α,α−トリフルオロ−o−トリル)−2−チオ尿素、
1−ベンゾイル−3−P−トリル−チオ尿素、
1−ベンゾイル−3−フェニル−2−チオ尿素、
1−ベンゾイル−3−ピリジン−2−イルメチル−チオ尿素、
1−(ベンゾイルアミジノ)−2−チオ尿素、
1−ベンジル−1−ブチル−3−フェニル−2−チオ尿素、
1−ベンジル−1−エチル−3−フェニル−2−チオ尿素。
1−ベンジル−3−(2−メチルベンゾイル)−チオ尿素、
1−ベンジル−3−(2−フェノキシプロピオニル)−2−チオ尿素、
1−ベンジル−3−(4−クロロ−2−(トリフルオロメチル)フェニル)−2−チオ尿素、
1−ベンジル−3−(4−フルオロ−3−ニトロフェニル)−2−チオ尿素、
1−ベンジル−3−(4−トルフルオロメチルスルファニルフェニル)−チオ尿素、
1−ベンジル−3−シンナモイル−2−チオ尿素、
1−ベンジル−3−シクロヘキシル−1−エチル−3−フェニル−2−チオ尿素、
1−ベンジル−3−フルフリル−2−チオ尿素、
1−ベンジル−3−メチル−2−チオ尿素、
1−ベンジル−3−フェニル−2−チオ尿素、
1−ブチル−2−チオ尿素、
1−ブチル−3−(2−ピリジル)−2−チオ尿素、
1−ブチル−3−(4−イソプロピルフェニル)−2−チオ尿素、
1−ブチル−3−フェニル−2−チオ尿素、
1−シンナモイル−3−(4−エトキシフェニル)−2−チオ尿素、
1−シンナモイル−3−(4−ヒドロキシフェニル)−2−チオ尿素、
1−シアノ−3−メチルイソチオ尿素、ナトリウム塩
1−シクロドデシル−3−(4−エトキシフェニル)−2−チオ尿素、
1−シクロヘキシル−1−メチル−3−フェニル−2−チオ尿素、
1−シクロヘキシル−3−(2−エトキシフェニル)−2−チオ尿素、
1−シクロヘキシル−3−(2−モルホリノエチル)−2−チオ尿素、
1−シクロヘキシル−3−(4−エトキシフェニル)−2−チオ尿素、
1−シクロヘキシル−3−フェニル−2−チオ尿素。
1−ジフェニルメチル−3−(2−フェネチル)−2−チオ尿素、
1−ドデカノイル−2−チオ尿素、
1−ドデカノイル−3−(1−ナフチル)−2−チオ尿素、
1−(ドデカノイル)−3−(2−エトキシフェニル)−2−チオ尿素、
1−ドデカノイル−3−(2−メトキシ−4−ニトロフェニル)−2−チオ尿素、
1−ドデカノイル−3−(2−メチル−4−ニトロフェニル)−2−チオ尿素、
1−ドデカノイル−3−(2−メチル−5−ニトロフェニル)−2−チオ尿素、
1−ドデカノイル−3−(2−ナフチル)−2−チオ尿素、
1−ドデカノイル−3−(2−ピリミジニル)−2−チオ尿素、
1−ドデカノイル−3−(2−(トルフルオロメチル)フェニル)−2−チオ尿素、
1−ドデカノイル−3−(4−メトキシフェニル)−2−チオ尿素、
1−ドデカノイル−3−(4−(N−メチルアセトアミド)フェニル)−2−チオ尿素、
1−ドデシル−3−フェニル−2−チオ尿素、
1−エチル−3−(2−フルオロフェニル)−2−チオ尿素、
1−エチル−3−(2−メトキシ−5−メチルフェニル)−2−チオ尿素、
1−エチル−3−(3,4−キシリル)−2−チオ尿素、
1−エチル−3−(4−ニトロフェニル)−2−チオ尿素、
1−エチル−3−(M−トリル)−2−チオ尿素、
1−エチル−3−(p−トリル)−2−チオ尿素、
1−エチル−3−フェニル−2−チオ尿素、
1−(フラン−2−カルボニル)−3−(2−トリフルオロメチル−フェニル)−チオ尿素、
1−(フラン−2−カルボニル)−3−(5−メチル−ピリジン−2−イル)−チオ尿素。
1−フラン−2−イルメチル−3−(2−メチルベンゾイル)−チオ尿素、
1−フラン−2−イルメチル−3−(4−(1,1,2,2,3,3,3−ヘプタフルオロ−プロピルスルファニル−フェニル)−チオ尿素、
1−フラン−2−イルメチル−3−(4−ニトロ−ベンゾイル)−チオ尿素、
1−フルフリル−3−(1−ナフチル)−2−チオ尿素、
1−フルフリル−3−フェニル−2−チオ尿素、
1−ヘキサデカノイル−2−チオ尿素、
1−ヘキサデシル−3−フェニル−2−チオ尿素、
1−(ヘキサメチレンイミノ)−3−(3−(トリフルオロメチル)フェニル)−2−チオ尿素、
1−イソブチル−3−フェニル−2−チオ尿素、
1−イソプロピル−3−(1−ナフチル)−2−チオ尿素、
1−イソプロピル−3−(3−(トルフルオロメチル)フェニル)−2−チオ尿素、
1−(イソプロピル)−3−(4−メチル−3−ニトロフェニル)−2−チオ尿素、
1−イソプロピル−3−フェニル−2−チオ尿素、
1−メチルアリル−3−メチル−2−チオ尿素、
1−メチル−1−(4−オクチルオキシフェニル)−2−チオ尿素、
1−メチル−3−(2,4,5−トリクロロフェニル)−2−チオ尿素、
1−メチル−3−(2,6−キシリル)−2−チオ尿素、
1−メチル−3−フェニル−2−チオ尿素、
1−メチル−3−プロピル−2−チオ尿素、
1−(ナフタレン−1−カルボニル)−3−m−トリル−チオ尿素
1−(ナフタレン−1−カルボニル)−3−フェニル−チオ尿素、
1−(ナフタレン−2−カルボニル)−3−(3−ニトロ−フェニル)−チオ尿素。
1−オクタデシル−3−フェニル−2−チオ尿素、
1−フェネチル−3−フェニル−2−チオ尿素、
1−フェニル−3−(1,2,4)トリアゾール−4−イル−チオ尿素、
1−フェニル−3−(2−(2−ピリジル)エチル)−2−チオ尿素、
1−フェニル−3−(2−(3−フェニル−チオウレイド)−シクロヘキシル)−チオ尿素、
1−フェニル−3−(2,6−キシリル)−2−チオ尿素、
1−フェニル−3−(2−ピリジル)−2−チオ尿素、
1−フェニル−3−(2−チアゾリル)−2−チオ尿素(2)、
1−フェニル−3−(3−ピリジル)−2−チオ尿素、
1−フェニル−3−(3−ピリジルメチル)−2−チオ尿素、
1−フェニル−3−(4−(3−フェニル−チオウレイド)−フェニル)−チオ尿素、
1−フェニル−3−(4−トリフルオロメチルベンジル)−チオ尿素、
1−フェニル−3−(5−フェニル−1,2,4−チアジアゾール−3−イル)−2−チオ尿素、
1−フェニル−3−(p−トリル)−2−チオ尿素、
1−フェニル−3−(p−トリルスルホニル)−2−チオ尿素、
1−フェニル−3−プロピル−2−チオ尿素、
1−フェニル−3−テトラデシル−2−チオ尿素、
1−ピリジン−3−イルメチル−3−(2−トリフルオロメチル−フェニル)−チオ尿素、
1−t−ブチル−3−フェニル−チオ尿素、
2−(1,1−ジオキソ−2,5−ジヒドロ−1H−チオフェン−3−イルメチル)−イソチオ尿素、塩酸塩。
2−(2−シアノ−エチル)イソチオ尿素、
2−(3−カルバンイミドイルスルファニル−ME−2,4,6−トリ−ME−ベンジル)−イソチオ尿素、
2−(3−カルバンイミドイルスルファニルメチル−ベンジル)−イソチオ尿素、
2−(3−カルバンイミドイルスルファニルメチル−ベンジル)−イソチオ尿素、
(2,3−ジフルオロフェニル)チオ尿素、
(2,3−ジメチルフェニル)−チオ尿素、
2−(3−フェニルブチル)イソチオ尿素、
(2,4,6−トリメチル−フェニル)−チオ尿素、
2−(4−カルバンイミドイルスルファニルメチル−ベンジル)−イソチオ尿素、
2−(4−カルバンイミドイルスルファニルメチル−ベンジル)−イソチオ尿素、
(2,4−ジフルオロフェニル)チオ尿素、
2−(4−ヒドロキシ−1,1−ジオキソ−テトラヒドロ−チオフェン−3−イル)イソチオ尿素、
2−(4−ME−1,1−ジオキソ−4H−チオフェン−3−イル)−イソチオ尿素、
2−(4−メチル−1,1−ジオキソ−2,3−ジヒドロ−1H−チオフェン−3−イル)−イソ尿素、
2−(4−メチル−1,1−ジオキソ−2,5−ジヒドロ−1H−チオフェン−3−イル)−イソ尿素、
(2,5−ジフルオロフェニル)チオ尿素、
2−(6−カルバンイミドイルスルファニル−ME−ナフタレン−2−イル−ME)−イソチオ尿素、
(2,6−ジフルオロフェニル)チオ尿素、
2−ベンゾイル−イソチオ尿素。
2−ヒドロキシ−3−イミノメチル−安息香酸、チオ尿素との化合物、
(3,4,5−トリメトキシ−フェニル)−チオ尿素、
3−(4−クロロフェニル)−1,1−ジメチル−2−チオ尿素、
3−(アダマンタン−1−カルボニル)−1,1−ジエチル−チオ尿素、
3−アリル−1−(3−クロロベンジル)−1−メチル−2−チオ尿素、
3−ベンゾイル−1,1−ジアリル−2−チオ尿素、
3−ベンゾイル−1,1−ジメチル−2−チオ尿素、
3−ベンゾイル−1,1−ジメチル−2−チオ尿素、
(3−ジメチルアミノ−プロピル)−チオ尿素、
(3−フルオロフェニル)チオ尿素、
[3−(トリフルオロメチル)フェニル]チオ尿素、
(4−エトキシ−フェニル)−チオ尿素、
(4−フルオロフェニル)チオ尿素、
アセチルチオ尿素、
エチレンビス(イソチオ尿素)、
N−(1,1−ジオキシドテトラヒドロ−3−チエニル)−N’−(2−フロイル)−N−メチルチオ尿素、
N’−(1,3−ジメチル−2,4−ジオキソ−1,2,3,4−テトラヒドロ−5−ピリミジニル)N,N−ジメチルチオ尿素、
N−((1,3−ジオキソ−3,4−ジヒドロ−2(1H)−ナフタレニリデン)メチル)−N’−オクタデシルチオ尿素、
N−(1−(4−BR−フェニル)エチリデン)−N’−(4−ME−6−オキソ−1,6−ジヒドロ−2−ピリミジニル)チオ尿素。
N−(1−メチル−2−プロペニル)−N’−(4−モルホリニル)チオ尿素、
N−(2−((1,1,2,2,3,3,3−ヘプタフルオロプロピル)チオ)フェニル)−N’−(2−チエニルカルボニル)チオ尿素、
N−(2−((2,4−ジクロロベンジル)スルホニル)−2−(2,4−ジクロロフェニル)ビニル)チオ尿素、
N−(2,2−ジシアノビニル)チオ尿素、
N−(2,2−ジメチルプロパノイル)−N’−(2−ニトロフェニル)チオ尿素、
N−(2−(2−オキソ−1−ピルロリジニル)エチル)−N’−フェニルチオ尿素、
N−(2−(3,4−ジメトキシ−PH)ET)−N’−((2,4−ジオキソ−2H−クロメン−3(4H)−イリデン)メチル)チオ尿素、
N−(2,3−ジクロロフェニル)−N’−(2−メチル−3−フロイル)チオ尿素、
N−(2,3−ジヒドロ−1,4−ベンゾジオキシン−2−イルメチル)−N’−(4−メチルベンゾイル)チオ尿素、
N−(2,4,6−トリクロロフェニル)チオ尿素、
N−((2,4,6−トリオキソテトラヒドロ−5(2H)−ピリミジニリデン)メチル)チオ尿素、
N−(2,4−ジクロロベンゾイル)−N’−(2−ピリジニルメチル)チオ尿素、
N−(2,4−ジクロロベンゾイル)−N’−(テトラヒドロ−2−フラニルメチル)チオ尿素、
N−(2,4−ジクロロフェニル)−N’−(2,2,2−トリクロロ−1−(ホルミルアミノ)エチル)チオ尿素、
N−(2,4−ジクロロフェニル)−N’−(2−メチルベンゾイル)チオ尿素、
N−(2,4−ジフルオロフェニル)−N’−(2−メチルベンゾイル)チオ尿素、
N−(2,4−ジクロロフェニル)−N’−(3−メチル−2−フロイル)チオ尿素。
N−(2,4−ジメチルフェニル)−N’−(2−メチルベンゾイル)チオ尿素、
N−(2,4−ジメチルフェニル)−N’−(3−フロイル)チオ尿素、
N−(2,4−ジメチルフェニル)−N’−(3−メチル−2−フロイル)チオ尿素、
N−(2,4−ジメチルフェニル)−N’−(4−メチルベンゾイル)チオ尿素、
N−(2,4−ジメチルフェニル)チオ尿素、
N−((2,4−ジオキソ−1,2,3,4−テトラヒドロ−3−キノリニル)メチル)−N’−ヘキシルチオ尿素、
N−(2,4−ジオキソ−1,2,3,4−テトラヒドロ−5−ピリミジニル)−N’−(4−メチルベンゾイル)チオ尿素、
N−((2,4−ジオキソ−2H−クロメン−3(4H)−イリデン)メチル)−N’−オクタデシルチオ尿素、
N−((2,4−ジオキソ−2H−クロメン−3(4H)−イリデン)メチル)−N’−フェニルチオ尿素、
N−(2,5−ジクロロフェニル)−N’−(2,2,2−トリクロロ−1−(ホルミルアミノ)エチル)チオ尿素、
N−(2,5−ジクロロフェニル)チオ尿素、
N−(2,6−DI−ME−PH)−N’−((2,4−ジオキソ−1,4−ジヒドロ−3(2H)−キノリニリデン)ME)チオ尿素、
N−(2,6−ジクロロフェニル)−N’−(3−フロイル)チオ尿素、
N−(2,6−ジクロロフェニル)−N’−(5−メチル−2−フロイル)チオ尿素、
N−(2−ベンゾイル−3−オキソ−3−フェニル−1−プロペニル)−N’−(2−t−ブチル−6−エチルフェニル)チオ尿素、
N−(2−(ベンジルスルフィニル)−2−フェニルビニル)−N’−(2,4−ジメチルフェニル)チオ尿素。
N−(2−(ベンジルスルフィニル)−2−フェニルビニル)−N’−フェニルチオ尿素、
N−(2−ブロモベンゾイル)−N’−(2−フリルメチル)チオ尿素、
N−(2−クロロベンゾイル)−N’−(5−(3−(2−フリル)アクリロイル)−4−ME−1,3−チアゾール−2−イル)チオ尿素、
N−(2−クロロフェニル)−N’−((6−ME−2,4−ジオキソ−2H−ピラン−3(4H)−イリデン)メチル)チオ尿素、
N−(2−フルオロフェニル)−N’−(2−メチル−3−フロイル)チオ尿素、
N−(2−フルオロフェニル)−N’−(3−メチル−2−フロイル)チオ尿素、
N−(2−フルオロフェニル)−N’−(5−メチル−2−フロイル)チオ尿素、
N−(2−フロイル)−N’−(4−メチルフェニル)チオ尿素、
N−(2−フロイル)−N’−(4−(トリフルオロメトキシ)フェニル)チオ尿素、
N−(2−MEO−ベンジリデン)−N’−(4−ME−6−オキソ−1,6−ジヒドロ−2−ピリミジニル)チオ尿素、
N−(2−メチル−3−フロイル)−N’−(4−(トリフルオロメチル)フェニル)チオ尿素、
N−(2−メチルベンゾイル)−N’−(2−ピリジニル)チオ尿素、
N−(2−メチルフェニル)−N’−(3−メチル−5−チオキソ−1,5−ジヒドロ−4H−1,2,4−トリアゾール−4−イル)チオ尿素、
N−(3−((1,1,2,2,3,3,3−ヘプタフルオロプロピル)チオ)PH)−N’−(2−チエニルカルボニル)チオ尿素、
N−(3,4−DI−CL−ベンゾイル)−N’−(5−(3−(2−フリル)アクリロイル)−4−ME−1,3−チアゾール−2−イル)チオ尿素。
N−(3,4−ジクロロフェニル)−N’−(5−メチル−2−フロイル)チオ尿素、
N−(3,4−ジヒドロ−2H−ピロール−5−イル)−N−フェニルチオ尿素、
N−(3,4−ジメトキシベンジリデン)−N’−(4−ME−6−オキソ−1,6−ジヒドロ−2−ピリミジニル)チオ尿素、
N−(3,4−ジメチルフェニル)チオ尿素、
N−(3,5−ビス(トリフルオロメトキシ)フェニル)−N’−(3−フロイル)チオ尿素、
N−(3,5−ジブロモ−2−ピリジニル)−N’−(2−チエニルカルボニル)チオ尿素、
N−(3,5−ジブロモ−2−ピリジニル)−N’−(4−メチルベンゾイル)チオ尿素、
N−(3−アセトアミドフェニル)チオ尿素、
N−(3−BR−ベンゾイル)−N’−(5−(3−(3−BR−フェニル)アクリロイル)−4−ME−1,3−チアゾール−2−イル)チオ尿素、
N−(3−カルボキルフェニル)チオ尿素、
N−(3−(ジフルオロメチル)チオ)フェニル)−N’−(2−チエニルカルボニル)チオ尿素、
N−(3−エトキシ−4−HO−ベンジリデン)−N’−(4−ME−6−オキソ−1,6−ジヒドロ−2−ピリミジニル)チオ尿素、
N−(3−フルオロフェニル)チオ尿素、
N−(3−フロイル)−N’−(4−ヨードフェニル)チオ尿素、
N−(3−フロイル)−N’−(4−メトキシフェニル)チオ尿素、
N−(3−フロイル)−N’−(4−(トリフルオロメチル)フェニル)チオ尿素、
N−(3−ヒドロキシフェニル)チオ尿素。
N−(3−メトキシフェニル)チオ尿素、
N−(3−メトキシ−2−ブテノイル)−N’−フェニルチオ尿素、
N−(3−メチル−2−フロイル)−N’−(3−(トリフルオロメチル)フェニル)チオ尿素、
N−(3−メチル−2−フロイル)−N’−(4−メチルフェニル)チオ尿素、
N−(3−メチル−2−フロイル)−N’−(4−(トリフルオロメチル)フェニル)チオ尿素、
N−((3−メチル−5−オキソ−1−フェニル−1,5−ジヒドロ−4H−ピラゾール−4−イリデン)メチル)チオ尿素、
N−(3−メチル−5−チオキソ−1,5−ジヒドロ−4H−1,2,4−トリアゾール−4−イル)−N’−フェニルチオ尿素、
N−(3−メチルフェニル)−N’−(3−メチル−5−チオキソ−1,5−ジヒドロ−4H−1,2,4−トリアゾール−4−イル)チオ尿素、
N−(3−メチルフェニル)−N’−(4−メチル−1−ピペラジニル)チオ尿素、
N−(3−(トリフルオロメチル)フェニル)−N’−(1,2,2−トリメチルプロピル)チオ尿素、
N−(4−(2−チエニル)−1,3−チアゾール−2−イル)チオ尿素、
N−(4−((4−フルオロベンジル)チオ)フェニル)−N’−(4−メトキシフェニル)チオ尿素、
N−(4−(4−モルホリニル)フェニル)−N’−(2−チエニルカルボニル)チオ尿素、
N−(4−(4−モルホリニル)フェニル)−N’−(4−ニトロベンゾイル)チオ尿素、
N−(4−アセトアミドフェニル)チオ尿素、
N−(4−ブロモベンジリデン)−N’−(6−ME−5−オキソ−4,5−ジヒドロ−1,2,4−トリアジン−3−イル)チオ尿素。
N−(4−カルボキシルフェニル)チオ尿素、
N−(4−クロロベンジリデン)−N’−(4−メチル−6−オキソ−1,6−ジヒドロ−2−ピリミジニル)チオ尿素、
N−((4−クロロフェノキシ)アセチル)−N’−(2−ニトロフェニル)チオ尿素、
N−(4−クロロフェニル)−N’−(2,4−ジクロロベンゾイル)チオ尿素、
N−(4−クロロフェニル)−N’−(2−フロイル)チオ尿素、
N−(4−クロロフェニル)−N’−(2−メチル−3−フロイル)チオ尿素、
N−(4−クロロフェニル)−N’−(3−メチル−2−フロイル)チオ尿素、
N−(4−(ジフルオロメチル)チオ)フェニル)−N’−(2−チエニルカルボニル)チオ尿素、
N−(4−(ジフルオロメチル)チオ)フェニル)−N’−(フェニルアセチル)チオ尿素、
N−(4−エトキシフェニル)−N’−(4−メチル−1−ピペラジニル)チオ尿素、
N−(4−エトキシフェニル)チオ尿素、
N−(4−フルオロフェニル)−N’−(2−メチル−3−フロイル)チオ尿素、
N−(4−フルオロフェニル)−N’−(3−メチル−2−フロイル)チオ尿素、
N−(4−フルオロフェニル)−N’−(4−メチルベンゾイル)チオ尿素、
N−(4−フルオロフェニル)−N’−(5−メチル−2−フロイル)チオ尿素、
N−(4−フルオロフェニル)−N’−(フェニル(((フェニルスルホニル)メチル)イミノ)メチル)チオ尿素、
N−(4−フルオロフェニル)チオ尿素、
N−(4−ヒドロキシフェニル)チオ尿素、
N−(4−ヨードフェニル)−N’−(2−メチル−3−フロイル)チオ尿素。
N−(4−メトキシベンジリデン)−N’−(4−メチル−6−オキソ−1,6−ジヒドロ−2−ピリミジニル)チオ尿素、
N−(4−メトキシベンジリデン)−N’−(6−ME−5−オキソ−4,5−ジヒドロ−1,2,4−トリアジン−3−イル)チオ尿素、
N−(4−メトキシフェニル)−N’−(2−メチル−3−フロイル)チオ尿素、
N−(4−メチルフェニル)−N’−(3−メチル−5−チオキソ−1,5−ジヒドロ−4H−1,2,4−トリアゾ−ル−4−イル)チオ尿素、
N−(4−メトキシフェニル)チオ尿素、
N−(4−メチル−5−(3−(2−メチルフェニル)アクリロイル)−1,3−チオアゾール−2−イル)チオ尿素、
N−(4−メチル−5−(3−(3−ニトロフェニル)アクリロイル)−1,3−チオアゾール−2−イル)チオ尿素、
N−(4−メチル−6−オキソ−1,6−ジヒドロ−2−ピリミジニル)−N’−(2−ニトロベンジリデン)チオ尿素、
N−(4−メチルベンゾイル)−N’−(4−(1−ピペリジニル)フェニル)チオ尿素、
N−(4−メチルフェニル)−N’−(フェニル(((フェニルスルホニル)メチル)イミノ)メチル)チオ尿素、
N−(4−メチルフェニル)チオ尿素、
N−(4−ニトロベンゾイル)−N’−(1,3−チアゾール−2−イル)チオ尿素、
N−(4−ニトロベンゾイル)−N’−(4−ニトロフェニル)チオ尿素、
N−(4−スルファモイル)フェニル)チオ尿素、
N−(4−t−ブチルフェニル)−N’−(2−メチル−3−フロイル)チオ尿素、
N−(4−tert−ブチルフェニル)−N’−(2−メチルベンゾイル)チオ尿素。
N−(4−tert−ブチルフェニル)−N’−(3−フロイル)チオ尿素、
N−(4−t−ブチルフェニル)−N’−(3−メチル−2−フロイル)チオ尿素、
N−(5−(2,4−ジクロロフェニル)−1,3,4−オキサジアゾール−2−イル)チオ尿素、
N−(5−(3−(2,4−ジクロロフェニル)アクリロイル)−4−メチル−1,3−チオアゾール−2−イル)チオ尿素、
N−(5−(3−(2−フリル)アクリロイル)−4−メチル−1,3−チオアゾール−2−イル)−N’−ヘキサノイルチオ尿素、
N−(5−(3−(2−フリル)アクリロイル)−4−メチル−1,3−チオアゾール−2−イル)−N’−パルミトイルチオ尿素、
N−(5−(3−(2−フリル)アクリロイル)−4−メチル−1,3−チオアゾール−2−イル)−N’−プロピオニルチオ尿素、
N−(5−(3−(2−HO−PH)アクリロイル)−4−ME−1,3−チオアゾール−2−イル)−N’−(4−ニトロベンゾイル)チオ尿素、
N−(5−(3−(3,4−ジメトキシフェニル)アクリロイル)−4−メチル−1,3−チオアゾール−2−イル)チオ尿素、
N−(5−(3−(3−ブロモフェニル)アクリロイル)−4−ME−1,3−チオアゾール−2−イル)−N’−イソブチルチオ尿素、
N−(5−(3−(3−ブロモフェニル)アクリロイル)−4−メチル−1,3−チオアゾール−2−イル)−N’−プロピオニルチオ尿素、
N−(5−(3−(4−クロロフェニル)アクリロイル)−4−メチル−1,3−チオアゾール−2−イル)チオ尿素、
N−(5−(3−(4−メトキシフェニル)アクリロイル)−4−メチル−1,3−チオアゾール−2−イル)チオ尿素。
N−(5−ブロモ−2−メトキシベンジル)−N−(4−イソプロピルフェニル)−N’−フェニルチオ尿素、
N−(5−メチル−2−フロイル)−N’−(2−(トリフルオロメチル)フェニル)チオ尿素、
N−(5−(フェノキシメチル)−1,3,4−オキサジアゾール−2−イル)チオ尿素、
N−(6−(1,3−ジオキソ−1,3−ジヒドロ−2H−イソインドール−2−イル)ヘキサノイル)−N’−(2−メト−フェニル)チオ尿素、
N−((6−メチル−2,4−ジオキソ−2H−ピラン−3(4H)−イリデン)メチル)−N’−オクラデシルチオ尿素、
N−((6−メチル−2,4−ジオキソ−2H−ピラン−3(4H)−イリデン)メチル)−N’−フェニルチオ尿素、
N−((6−メチル−2,4−ジオキソ−2H−ピラン−3(4H)−イリデン)メチル)−フェニルチオ尿素、
N−(9−アントリルメチル)−N’−ベンゾイル−N−メチルチオ尿素、
N−アリル−N’−((2,4−ジオキソ−1,2,3,4−テトラヒドロ−3−キノリニル)メチル)チオ尿素、
N−アリル−N’−((2,4−ジオキソ−2H−クロメン−3(4H)−イリデン)メチル)チオ尿素、
N−アリル−N’−(4−メチル−1−ピペラジニル)チオ尿素、
N−アリルチオ尿素(2)
N−ベンゾイル−N’−(1−ナフチル)チオ尿素。
N−ベンゾイル−N’−(3−メチルフェニル)チオ尿素、
N−ベンゾイル−N’−(3−ピリジニル)チオ尿素、
N−ベンゾイル−N’−(4−クロロフェニル)チオ尿素、
N−ベンゾイル−N’−(4−メチル−6−オキソ−1,6−ジヒドロ−2−ピリミジニル)チオ尿素、
N’−ベンゾイル−N,N−ジエチルチオ尿素、
N’−ベンゾイル−N,N−ジヘキシルチオ尿素、
N’−ベンゾイル−N,N−ジイソブチルチオ尿素、
N−ベンジル−N’−((1,3−ジオキソ−1,3−ジヒドロ−2H−イリデン−2−イリデン)メチル)チオ尿素、
N−ベンジル−N’−(1,3−チアゾール−2−イル)チオ尿素、
N−ベンジル−N’−(2−ピリジニル)チオ尿素、
N−ベンジル−N’−(3−(4−BR−PH)−5−チオキソ−1,5−ジヒドロ−4H−1,2,4−トリアゾール−4−イル)チオ尿素、
N−ベンジル−N’−(フェニル(フェニエチルイミノ)メチル)チオ尿素、
N−Boc−チオ尿素、
N−ブチル−N’−((2,4−ジオキソ−1,4−ジヒドロ−3(2H)−キノリニリデン)メチル)チオ尿素、
N−シクロヘキシル−N’−(1−フェニルエチル)チオ尿素、
N’−シクロヘキシル−N,N−ジイソブチルチオ尿素、
N−ダンシル−N’−エチルチオ尿素、
N−デシル−N’−(2−ヒドロキシエチル)チオ尿素、
N−エチル−N’−(3−メトキシ−2−ブテノイル)−N−フェニルチオ尿素、
V−エチルチオ尿素(2)。
N−メタリル−N’−メチルチオ尿素、
N−メチルチオ尿素(2)
N,N−ビス(2−シアノエチル)−N’−ヘキシルチオ尿素、
N,N’−ビス(4−エトキシフェニル)チオ尿素、
N,N’−ジ−Boc−S−メチルイソチオ尿素、
N,N’−ジ−(t−ブトキシカルボニル)チオ尿素、
N,N’−ジブチルチオ尿素(2)、
N,N’−ジエチルチオ尿素、
N,N’−ジメチルチオ尿素、
N,N’−ジフェニルチオ尿素、
N,N’−ジフェニルチオ尿素、
N’−オクタデシルフルオレセイン−5−チオ尿素、
N−フェニル−N’−(フェニル(フェニルイミノ)メチル)チオ尿素、
N−フェニル−N’−(テトラヒドロ−2−フラニルメチル)チオ尿素、
N−フェニルチオ尿素、
N−フェニルチオ尿素、
N−(t−ブチル)−N’−(3−(トリフルオロメチル)フェニル)チオ尿素、
(フェニル−フェニルイミノ−メチル)−チオ尿素、
プロピルチオ尿素、
S−[(2−グアニジノ−4−チアゾイル)メチル]イソチオ尿素、
S−ベンジルイソチオ尿素、
S−エチルイソチオ尿素、
S−イソプロピルイソチオ尿素
S−メチル−N−(4−トルエンスルホニル)イソチオ尿素。
テトラメチルチオ尿素、チオ尿素
トルエン−4−スルホン酸、
2−(2−(1−オキシ−ピリジン−2−イル)エチル)−イソチオ尿素、
1,3−ビス(ベンジルオキシカルボニル)−2−メチル−2−チオプソイド尿素、
1,3−ビス(tert−ブトキシカルボニル)−2−メチル−2−チオプソイド尿素、
2−ベンジル−2−チオプソイド尿素、
2−エチル−2−チオプソイド尿素、
2−イミダゾリジンチオン
2−イミノ−4−チオビュレット
(アミジノチオ)酢酸
ホルムアミジンスルフィン酸
S−(2−アミノエチル)イソチオウロニウムブロミド。
適した充填剤は、特に石英粉およびガラスセラミック粉末、酸化アルミニウムおよび/または酸化珪素である。特に好ましい充填剤は、ガラス粉末、たとえばバリウムガラス粉末、バリウムシリケートガラス粉末、リチウム−またはアルミニウム−シリケートガラス粉末および微分散されたシリカ、たとえば熱分解法シリカまたは沈降シリカである。
処理時間を測定するために、二成分を1:1の割合で強力に撹拌した。ゲル化点までの時間が、ゲル化時間として示され、かつ最大処理時間を調整するために観察することができる。官能的認知には、確かに個々の変動幅が存在するが、これはさらに系の構成比に依存する。開始剤の特徴を把握するための付加的な方法として、熱のトーン(Waermtoenung)を熱量的に記録する。温度上昇の開始を、重要な測定点として定める。これらの測定は、調製物の銅含量に依存する、確実な調整可能な処理時間を示す。これに関して、開始剤系の活性の変動幅は、多い銅含量(0.1%)での<10sの特に短い阻害時間から、さらに銅化合物が欠如する際の、極めて長い阻害時間またはそれどころか重合の不発生まで達する。
個々の成分は、50℃の温度で長期に亘って貯蔵される。処理時間の変化は、最大5ヶ月の期間に亘って記録される。これに関して試料は、同様に50℃または室温(RT)で貯蔵された2種の成分についておこなう。
重合された(メタ)アクリレートの色は、当然のことながら着色された銅イオン含量に左右される。ポリマーの着色と銅化合物の割合との関係は、試験体の色測定によって算出される。これに関して、特に重要であるのは、色の恒常性(Farbkonstanz)である。
測定のために、1mmの厚さを有する試験体を製造し、かつ48時間の貯蔵後に測定した。透明なポリマー層のCIE−Lab−値は、白色の背景の前で確認される。色安定性は、7日間に亘って、40℃の温度で試験される。これに関して、層の変色は観察することはできなかった。さらに長時間の貯蔵後であっても、顕著な色の変化は生じることがないことから、本発明による銅化合物を有する開始剤系は、歯科材料に要求される審美的条件を十分に充たすものである。
Claims (33)
- 以下の成分
(a)第3級炭素と結合している1個または複数個のヒドロペルオキシド基を有するヒドロペルオキシド化合物;
(b)チオ尿素誘導体;
(c)促進剤として、調製物中で溶解性の銅化合物
を有する、重合可能な材料を硬化させるための促進剤を有する二成分開始剤系。 - (a)酸官能基を有しない重合可能なモノマー少なくとも1種、その際、重合可能な基は、アクリレート、メタクリレート、ビニル基またはビニルシクロプロパンの構造単位を含有し;
(b)第3級炭素と結合している1個または複数個のヒドロペルオキシド基を有するヒドロペルオキシド化合物;
(c)チオ尿素誘導体;
(d)調製物中で溶解性の銅化合物;
(e)場合によっては、カルボン酸、酸無水物、スルホン酸、スルフィン酸、リン酸エステル、ホスホン酸エステル、ホスホン酸塩またはホスフィン酸塩から選択された酸官能基少なくとも1種を含有する1種または複数個の接着性モノマー;
(f)少なくとも1種の安定化剤;
(g)場合によっては、光開始剤、分散された充填剤、溶剤またはこれらの組み合わせ物、を含有する歯科用組成物。 - 銅化合物を、少なくとも0.0001質量%、多くとも5質量%の割合で含有する、請求項2に記載の歯科用組成物。
- 銅化合物を、少なくとも0.01質量%、多くとも5質量%の割合で含有する、請求項2に記載の歯科用組成物。
- 酸性化合物を、少なくとも0.1%の割合で含有する、請求項2に記載の歯科用組成物。
- 酸性化合物を、少なくとも1%の割合で含有する、請求項2に記載の歯科用組成物。
- 酸性化合物を、少なくとも10%の割合で含有する、請求項2に記載の歯科用組成物。
- 二成分に分けられ、その際、二成分系の一の組成物は、ヒドロペルオキシドを含有し、かつ第二の調製物は、チオ尿素誘導体および少なくとも1種の銅化合物を含有する、請求項2から7までのいずれか1項に記載の歯科用組成物。
- 二成分系が、液体/液体、ペースト/ペースト、ペースト/液体および粉体/液体の群からの、異なるかまたは同一のコンシステンシーの調製物の組み合わせである、請求項2から8までのいずれか1項に記載の歯科用組成物。
- 二成分系調製物が充填材料、セメント、割れ封止剤、プロテーゼ材料、プライマーまたは接着剤であってもよい、請求項2から9までのいずれか1項に記載の歯科用組成物。
- 二成分系が、組成(a)、(b)、(e)、(f)および微分散された充填剤から成る第一ペーストと、組成(a)、(c)、(d)、(e)、(f)および微分散された充填剤から成る第二ペーストとから成る、請求項2に記載の歯科用組成物。
- 二成分系の少なくとも一の成分が、構成成分(g)として光開始剤を含有し、かつ混合によりデュアル硬化される系を形成する、請求項2に記載の歯科用組成物。
- 調製物を充填材料として、セメントとして、プロテーゼ材料として、割れ封入剤としてまたは粘着性複合材料として使用することができる、請求項2から12までのいずれか1項に記載の歯科用組成物。
- 二成分系が、組成(a)、(b)、(e)、(f)および少なくとも1種の揮発性溶剤から成る第一液体と、組成(a)、(c)、(d)、(e)、(f)および少なくとも1種の溶剤から成る第二液体とから成る、請求項2に記載の歯科用組成物。
- 二成分がそれぞれ包装手段としての注入器中で調製される、請求項8から14までのいずれか1項に記載の歯科用組成物。
- 二成分が包装手段としての二室型注入器中で調製される、請求項8から14までのいずれか1項に記載の歯科用組成物。
- 二室型注入器の成分を、放出する際に、場合によっては上部に配置されたスタティックミキサによって、均一に混合することができる、請求項16に記載の歯科用組成物。
- 二成分がそれぞれ包装手段としての瓶中で調製される、請求項8に記載の歯科用組成物。
- 二成分がそれぞれ異なる包装手段中で(たとえば、注入器および瓶)調製される、請求項8または9に記載の歯科用組成物。
- 二成分が、包装手段としての二室型ディスペンサー中に別個に存在し、かつ放出させながら混合する、請求項9から11までのいずれか1項に記載の歯科用組成物。
- 材料が、粉末および液体の形で調製され、かつ、粉末が構成成分(c)、(d)を含有し、その一方で液体中に構成成分(a)、(b)、(f)および場合によっては(e)が含有されている、請求項2に記載の歯科用組成物。
- 無機性の金属酸化物、金属窒化物、金属塩、シリケートガラス、アルミノシリケートガラス、アルミノボロシリケートガラス、フルオロアルミノシリケートガラス、石英、コロイダルシリカ、熱分解法シリカ、沈降シリカ、シリカポリマー、酸化ジルコニウム−シリカ、ポリマー充填剤、含まれる無機性粒子と一緒に重合された複合材料充填剤およびこれらの組み合わせ物から構成されていてもよい、充填剤を含有する、請求項11から21までのいずれか1項に記載の歯科用組成物。
- 充填剤、たとえばSr、Y、Zr、Ba、La、Hf、Zn、Bi、W、ランタニドの群から選択された少なくとも1種の元素の金属酸化物、金属窒化物、金属塩、シリケートガラス、アルミノシリケートガラス、アルミノボロシリケートガラスおよびフルオロアルミノシリケートガラスまたはこれらの組み合わせ物を含有する、請求項22に記載の歯科用組成物。
- 溶剤として水、メタノール、エタノール、プロパノール、イソプロパノール、アセトン、メチルエチルケトン、エチレングリコール、グリセロールおよびこれらの組合せ物を含有していてもよい、請求項2から23のいずれか1項に記載の歯科用組成物。
- アクリレート、メタクリレートまたはビニル化合物の群から選択される、少なくとも1種のエチレン系不飽和基を有する、酸性の重合可能な化合物を含有する、請求項2から24までのいずれか1項に記載の歯科用組成物。
- リン酸エステル、ホスホン酸、ホスフィン酸、硫酸エステル、スルホン酸、スルフィン酸、硼酸エステル、ボロン酸またはカルボン酸の化合物からの、少なくとも1種の酸官能基を有する酸性モノマーを含有する、請求項25に記載の歯科用組成物。
- t−ブチルヒドロペルオキシド、t−アミルヒドロペルオキシド、イソ−プロピルベンゼンヒドロペルオキシド、p−ジイソプロピルベンゼンヒドロペルオキシド、5−フェニル−4−ペンテニルヒドロペルオキシド、ピナンヒドロペルオキシド、1,1,3,3−テトラメチルブチルヒドロペルオキシドの物質およびこれらの組合せ物から選択された、少なくとも1種のヒドロペルオキシド化合物を含有する、請求項2から26までのいずれか1項に記載の歯科用組成物。
- 二成分に分けられ、その際、二成分材料は、修復材的に、矯正歯科学的にまたは歯内療法的に使用可能な調製物である、請求項2から27までのいずれか1項に記載の歯科用組成物。
- 混合後の硬化時間が、15分未満である、請求項2から28までのいずれか1項に記載の歯科用組成物。
- 混合後の硬化時間が、5分未満である、請求項2から29までのいずれか1項に記載の歯科用組成物。
- 二成分を少なくとも2ヶ月に亘って50℃で貯蔵した後の、混合後の硬化時間が15分未満である、請求項2から30までのいずれか1項に記載の歯科用組成物。
- 二成分を少なくとも3ヶ月に亘って37℃で貯蔵した後の、混合後の硬化時間が15分未満である、請求項2から31までのいずれか1項に記載の歯科用組成物。
- アミン不含である、請求項1に記載の二成分開始剤系。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005039590A DE102005039590B4 (de) | 2005-08-19 | 2005-08-19 | Polymerisierbare Dentalzusammensetzung mit einem 2-Komponenten-Initiatorsystem |
DE102005039590.2 | 2005-08-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2007056020A true JP2007056020A (ja) | 2007-03-08 |
JP5773557B2 JP5773557B2 (ja) | 2015-09-02 |
Family
ID=37546844
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006224694A Active JP5773557B2 (ja) | 2005-08-19 | 2006-08-21 | 貯蔵安定性および酸系のための特別な適性 |
Country Status (8)
Country | Link |
---|---|
US (1) | US20070040151A1 (ja) |
EP (1) | EP1754465B1 (ja) |
JP (1) | JP5773557B2 (ja) |
CN (1) | CN101129295B (ja) |
AT (1) | ATE526937T1 (ja) |
BR (1) | BRPI0603389A (ja) |
CA (1) | CA2551973A1 (ja) |
DE (1) | DE102005039590B4 (ja) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010525067A (ja) * | 2007-04-25 | 2010-07-22 | デンツプライ インターナショナル インコーポレーテッド | 自己接着性歯科用セメント |
EP2230280A1 (en) | 2009-03-18 | 2010-09-22 | GC Corporation | Polymerizable composition |
EP2233544A1 (en) | 2009-03-25 | 2010-09-29 | GC Corporation | Polymerizable composition |
EP2371346A1 (en) | 2010-03-31 | 2011-10-05 | GC Corporation | Paste-type polymerizable composition |
JP2014152106A (ja) * | 2013-02-05 | 2014-08-25 | Tokuyama Dental Corp | 歯科用硬化性組成物 |
WO2014156077A1 (ja) | 2013-03-28 | 2014-10-02 | クラレノリタケデンタル株式会社 | 硬化性組成物 |
JP2014227370A (ja) * | 2013-05-21 | 2014-12-08 | クラレノリタケデンタル株式会社 | 硬化性組成物 |
JP2015522687A (ja) * | 2012-06-27 | 2015-08-06 | ヘンケル ユーエス アイピー エルエルシー | 2ステップ接着システムのための促進剤 |
US9125802B2 (en) | 2010-12-20 | 2015-09-08 | Kuraray Noritake Dental Inc. | Dental curable composition |
JP2017507984A (ja) * | 2014-03-20 | 2017-03-23 | イフォクレール ヴィヴァデント アクチェンゲゼルシャフトIvoclar Vivadent AG | チオ尿素誘導体に基づく光重合性およびデュアルキュア型歯科用材料 |
US9844494B2 (en) | 2014-03-24 | 2017-12-19 | Gc Corporation | Two-paste polymerizable compostion |
JP2018504447A (ja) * | 2015-02-09 | 2018-02-15 | ゼスト、アイピー、ホールディングス、リミテッド、ライアビリティー、カンパニーZest Ip Holdings,Llc | 歯科用組成物および使用方法 |
WO2019131094A1 (ja) | 2017-12-26 | 2019-07-04 | 株式会社トクヤマデンタル | 化学重合開始剤、接着性組成物、接着性組成物キット、歯科用材料、歯科用材料キットおよび接着性組成物の保管方法 |
WO2020111142A1 (ja) | 2018-11-28 | 2020-06-04 | クラレノリタケデンタル株式会社 | 歯科用接着材料キット |
JP2021102564A (ja) * | 2019-12-24 | 2021-07-15 | クラレノリタケデンタル株式会社 | 歯科用硬化性組成物 |
WO2022196757A1 (ja) * | 2021-03-19 | 2022-09-22 | サンメディカル株式会社 | 重合開始剤含有組成物および歯科用重合性組成物 |
WO2023058770A1 (ja) | 2021-10-08 | 2023-04-13 | クラレノリタケデンタル株式会社 | ペースト状の二剤型歯科用硬化性組成物 |
WO2023058773A1 (ja) | 2021-10-08 | 2023-04-13 | クラレノリタケデンタル株式会社 | 歯科用硬化性組成物及び歯科用キット |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102007015698B4 (de) * | 2007-03-27 | 2009-05-14 | Innotere Gmbh | Implantatmaterial auf Basis eines Polymersystems und dessen Verwendung sowie Applikationsset |
DE102007050763A1 (de) | 2007-10-22 | 2009-04-23 | Heraeus Medical Gmbh | Initiatorsystem für selbsthärtende Kunststoffe, seine Verwendung und es enthaltende Knochenzementzusammensetzungen |
DE202008009873U1 (de) | 2008-07-22 | 2008-10-02 | Kettenbach Gmbh & Co. Kg | Dentale Bleichmittelzusammensetzung und Dentallack |
EP2198824B1 (de) | 2008-12-22 | 2013-02-13 | Ernst Mühlbauer GmbH & Co.KG | Polymerisierbares Dentalmaterial mit Initiatorsystem |
DE102010024653B4 (de) | 2010-06-22 | 2012-06-21 | Heraeus Medical Gmbh | Kit zur Herstellung von Knochenzement und Verwendung dieses Kits |
JP2012051856A (ja) * | 2010-09-03 | 2012-03-15 | Gc Corp | 重合性組成物 |
US9365750B2 (en) | 2012-06-27 | 2016-06-14 | Henkel IP & Holding GmbH | Accelerators for curable compositions |
US10590311B2 (en) * | 2012-06-27 | 2020-03-17 | Henkel IP & Holding GmbH | Accelerators for two part curable compositions |
US8986847B2 (en) * | 2012-06-27 | 2015-03-24 | Henkel IP & Holding GmbH | Accelerator/oxidant/proton source combinations for two part curable compositions |
EP2921156B1 (de) | 2014-03-20 | 2019-10-02 | Ivoclar Vivadent AG | Monomermischung zur Herstellung von Dentalwerkstoffen |
CN103976884B (zh) * | 2014-06-04 | 2016-08-24 | 吉林省登泰克牙科材料有限公司 | 一种双固化牙科复合树脂材料 |
US9676922B2 (en) | 2014-06-11 | 2017-06-13 | IPS, Corporation—Weld-On Division | Heat and moisture resistant acrylic adhesive composition |
JP7109438B2 (ja) * | 2016-12-05 | 2022-07-29 | アーケマ・インコーポレイテッド | 重合開始剤ブレンド物、およびそのような重合開始剤ブレンド物を含む3dプリンティングに有用な光硬化性組成物 |
EP3338756B1 (de) | 2016-12-21 | 2020-02-26 | VOCO GmbH | Lagerstabiler kunststoffmodifizierter glasionomerzement |
US10751263B2 (en) * | 2017-04-03 | 2020-08-25 | Zest Ip Holdings, Llc | Dental cement compositions and methods of use |
WO2019031488A1 (ja) | 2017-08-07 | 2019-02-14 | 三井化学株式会社 | 分包型硬化性組成物 |
WO2019082964A1 (ja) | 2017-10-26 | 2019-05-02 | 三井化学株式会社 | 硬化性組成物 |
CN108642926B (zh) * | 2018-04-26 | 2023-11-14 | 浙江汉邦新材料股份有限公司 | 一种涤纶染色清洗用的硫脲衍生物及其制备方法 |
WO2020163414A1 (en) | 2019-02-07 | 2020-08-13 | Ips Corporation | Gasketed pipe joint formed in place and method of making same |
ES2918149T3 (es) | 2019-02-07 | 2022-07-14 | Ivoclar Vivadent Ag | Materiales dentales con comportamiento de fraguado mejorado |
ES2879378T3 (es) | 2019-02-07 | 2021-11-22 | Ivoclar Vivadent Ag | Materiales dentales a base de sistemas rédox con derivados de hidroperóxido de cumeno de olor reducido |
EP3692974B1 (de) * | 2019-02-07 | 2021-08-25 | Ivoclar Vivadent AG | Dentalmaterialien mit verbesserten mechanischen eigenschaften |
US11020324B2 (en) * | 2019-02-26 | 2021-06-01 | James R. Glidewell Dental Ceramics, Inc. | Dual-curing dental compositions with high stability |
ES2941670T3 (es) | 2021-01-21 | 2023-05-24 | Ivoclar Vivadent Ag | Material dental para la producción de coronas y puentes provisionales |
EP4039220B1 (de) | 2021-02-05 | 2022-12-28 | Ivoclar Vivadent AG | Dentalmaterialien auf der basis von polymerisationsfähigen thioharnstoff-derivaten |
EP4066811A1 (de) | 2021-03-31 | 2022-10-05 | Ivoclar Vivadent AG | Lagerstabiles dentaladhäsivset zur anwendung mit peroxidisch und hydroperoxidisch redoxinitiierten kompositen |
WO2022229734A1 (en) | 2021-04-29 | 2022-11-03 | 3M Innovative Properties Company | Initiator system with polymerizable thiourea component, dental composition and use thereof |
EP4094748B1 (de) | 2021-05-26 | 2023-09-20 | Ivoclar Vivadent AG | Dentalwerkstoffe auf basis von redoxsystemen mit oligomeren cumolhydroperoxid-derivaten |
EP4205723A1 (de) | 2021-12-29 | 2023-07-05 | Ivoclar Vivadent AG | Sulfathaltiger oder phosphataltiger, selbsthaftender dentaler kompositzement mit guter transparenz |
EP4205722A1 (de) | 2021-12-29 | 2023-07-05 | Ivoclar Vivadent AG | Selbsthaftender dentaler kompositzement mit guter transparenz |
EP4205724A1 (de) | 2021-12-29 | 2023-07-05 | Ivoclar Vivadent AG | Selbsthaftende dentale kompositzemente mit guter transparenz auf basis säurebehandelter füllstoffe |
EP4331557A1 (en) | 2022-09-01 | 2024-03-06 | Ivoclar Vivadent AG | Radically polymerizable composition comprising a redox initiator system based on dihydropyridines |
EP4356893A1 (de) | 2022-10-20 | 2024-04-24 | Ivoclar Vivadent AG | Lagerstabile selbsthaftende kompositzemente mit guter transparenz und guter röntgenopazität |
EP4414390A1 (en) | 2023-02-10 | 2024-08-14 | Ivoclar Vivadent AG | Acylthiourea oligomers suitable as redox initiator components and radically polymerizable compositions comprising them |
US11897856B1 (en) | 2023-10-12 | 2024-02-13 | King Faisal University | N-(Naphthalen-1-ylcarbamothioyl)furan-2-carboxamide as an eco-friendly insecticidal agent against Spodoptera littoralis (boisd.) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5516018A (en) * | 1978-07-19 | 1980-02-04 | Denki Kagaku Kogyo Kk | Acrylate curing composition |
JPS56169609A (en) * | 1980-04-29 | 1981-12-26 | Colgate Palmolive Co | Dental composition |
JPH02681A (ja) * | 1988-11-29 | 1990-01-05 | Denki Kagaku Kogyo Kk | アクリレートの硬化性組成物 |
JP2005008622A (ja) * | 2003-05-19 | 2005-01-13 | Kerr Corp | 二部式自己接着性歯科用組成物 |
JP2009503086A (ja) * | 2005-08-02 | 2009-01-29 | デンツプライ インターナショナル インコーポレーテッド | 歯科用組成物のための触媒系 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1177879A (en) * | 1967-09-04 | 1970-01-14 | Sumitomo Chemical Co | Catalyst System and process for the Polymerisation of Vinyl Compounds |
JPS58219281A (ja) | 1982-06-14 | 1983-12-20 | Mitsubishi Heavy Ind Ltd | 接水構造物における鋼板と銅板類の接着方法 |
JPH066608B2 (ja) * | 1985-08-06 | 1994-01-26 | 住友化学工業株式会社 | メタクリル酸エステル系重合体の製造方法 |
DE19501933A1 (de) | 1995-01-24 | 1996-07-25 | Henkel Kgaa | Aerob härtbarer Klebstoff |
US5688883A (en) * | 1995-03-14 | 1997-11-18 | Dentsply Gmbh | Polymerizable composition |
DE69942571D1 (de) * | 1998-04-23 | 2010-08-26 | Dentsply Detrey Gmbh | Lagerungsbeständige polymerisierbare Zusammensetzung |
DE19818210C5 (de) * | 1998-04-24 | 2007-02-08 | Ivoclar Vivadent Ag | Radikalisch polymerisierbarer Dentalwerkstoff |
US7275932B2 (en) * | 2001-09-20 | 2007-10-02 | Pentron Clinical Technologies, Llc | Self-curing system for endodontic sealant applications |
US7173074B2 (en) * | 2001-12-29 | 2007-02-06 | 3M Innovative Properties Company | Composition containing a polymerizable reducing agent, kit, and method |
DE10238833B4 (de) * | 2002-08-23 | 2005-09-29 | Ivoclar Vivadent Ag | Dentalprothese mit metallfreien Verankerungselementen |
US7214726B2 (en) * | 2003-07-17 | 2007-05-08 | Kerr Corporation | Methods of using two-part self-adhering dental compositions |
-
2005
- 2005-08-19 DE DE102005039590A patent/DE102005039590B4/de not_active Expired - Fee Related
-
2006
- 2006-07-10 US US11/483,488 patent/US20070040151A1/en not_active Abandoned
- 2006-07-11 CA CA002551973A patent/CA2551973A1/en not_active Abandoned
- 2006-08-05 AT AT06016385T patent/ATE526937T1/de active
- 2006-08-05 EP EP06016385A patent/EP1754465B1/de active Active
- 2006-08-21 BR BRPI0603389-0A patent/BRPI0603389A/pt not_active Application Discontinuation
- 2006-08-21 CN CN200610126248.8A patent/CN101129295B/zh active Active
- 2006-08-21 JP JP2006224694A patent/JP5773557B2/ja active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5516018A (en) * | 1978-07-19 | 1980-02-04 | Denki Kagaku Kogyo Kk | Acrylate curing composition |
JPS56169609A (en) * | 1980-04-29 | 1981-12-26 | Colgate Palmolive Co | Dental composition |
JPH02681A (ja) * | 1988-11-29 | 1990-01-05 | Denki Kagaku Kogyo Kk | アクリレートの硬化性組成物 |
JP2005008622A (ja) * | 2003-05-19 | 2005-01-13 | Kerr Corp | 二部式自己接着性歯科用組成物 |
JP2009503086A (ja) * | 2005-08-02 | 2009-01-29 | デンツプライ インターナショナル インコーポレーテッド | 歯科用組成物のための触媒系 |
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010525067A (ja) * | 2007-04-25 | 2010-07-22 | デンツプライ インターナショナル インコーポレーテッド | 自己接着性歯科用セメント |
EP2230280A1 (en) | 2009-03-18 | 2010-09-22 | GC Corporation | Polymerizable composition |
EP2233544A1 (en) | 2009-03-25 | 2010-09-29 | GC Corporation | Polymerizable composition |
US8247470B2 (en) | 2009-03-25 | 2012-08-21 | Gc Corporation | Polymerizable composition |
EP2371346A1 (en) | 2010-03-31 | 2011-10-05 | GC Corporation | Paste-type polymerizable composition |
US9125802B2 (en) | 2010-12-20 | 2015-09-08 | Kuraray Noritake Dental Inc. | Dental curable composition |
KR101858323B1 (ko) * | 2012-06-27 | 2018-05-15 | 헨켈 아이피 앤드 홀딩 게엠베하 | 이단계 접착제 시스템을 위한 촉진제 |
JP2015522687A (ja) * | 2012-06-27 | 2015-08-06 | ヘンケル ユーエス アイピー エルエルシー | 2ステップ接着システムのための促進剤 |
JP2014152106A (ja) * | 2013-02-05 | 2014-08-25 | Tokuyama Dental Corp | 歯科用硬化性組成物 |
US9889070B2 (en) | 2013-03-28 | 2018-02-13 | Kuraray Noritake Dental Inc. | Curable composition |
WO2014156077A1 (ja) | 2013-03-28 | 2014-10-02 | クラレノリタケデンタル株式会社 | 硬化性組成物 |
JP2014227370A (ja) * | 2013-05-21 | 2014-12-08 | クラレノリタケデンタル株式会社 | 硬化性組成物 |
JP2017507984A (ja) * | 2014-03-20 | 2017-03-23 | イフォクレール ヴィヴァデント アクチェンゲゼルシャフトIvoclar Vivadent AG | チオ尿素誘導体に基づく光重合性およびデュアルキュア型歯科用材料 |
US9844494B2 (en) | 2014-03-24 | 2017-12-19 | Gc Corporation | Two-paste polymerizable compostion |
JP2021073249A (ja) * | 2015-02-09 | 2021-05-13 | ゼスト、アイピー、ホールディングス、リミテッド、ライアビリティー、カンパニーZest Ip Holdings,Llc | 歯科用組成物および使用方法 |
JP2018504447A (ja) * | 2015-02-09 | 2018-02-15 | ゼスト、アイピー、ホールディングス、リミテッド、ライアビリティー、カンパニーZest Ip Holdings,Llc | 歯科用組成物および使用方法 |
US11259995B2 (en) | 2015-02-09 | 2022-03-01 | Zest Ip Holdings, Llc | Dental compositions and methods of use |
WO2019131094A1 (ja) | 2017-12-26 | 2019-07-04 | 株式会社トクヤマデンタル | 化学重合開始剤、接着性組成物、接着性組成物キット、歯科用材料、歯科用材料キットおよび接着性組成物の保管方法 |
KR20200057053A (ko) | 2017-12-26 | 2020-05-25 | 가부시키가이샤 도쿠야마 덴탈 | 화학중합개시제, 접착성 조성물, 접착성 조성물 키트, 치과용 재료, 치과용 재료 키트 및 접착성 조성물의 보관 방법 |
US11325993B2 (en) | 2017-12-26 | 2022-05-10 | Tokuyama Dental Corporation | Chemical polymerization initiator, adhesive composition, adhesive composition kit, dental material, dental material kit, and method of storing adhesive composition |
WO2020111142A1 (ja) | 2018-11-28 | 2020-06-04 | クラレノリタケデンタル株式会社 | 歯科用接着材料キット |
JP2021102564A (ja) * | 2019-12-24 | 2021-07-15 | クラレノリタケデンタル株式会社 | 歯科用硬化性組成物 |
JP7356338B2 (ja) | 2019-12-24 | 2023-10-04 | クラレノリタケデンタル株式会社 | 歯科用硬化性組成物 |
WO2022196757A1 (ja) * | 2021-03-19 | 2022-09-22 | サンメディカル株式会社 | 重合開始剤含有組成物および歯科用重合性組成物 |
WO2023058770A1 (ja) | 2021-10-08 | 2023-04-13 | クラレノリタケデンタル株式会社 | ペースト状の二剤型歯科用硬化性組成物 |
WO2023058773A1 (ja) | 2021-10-08 | 2023-04-13 | クラレノリタケデンタル株式会社 | 歯科用硬化性組成物及び歯科用キット |
Also Published As
Publication number | Publication date |
---|---|
EP1754465A1 (de) | 2007-02-21 |
CA2551973A1 (en) | 2007-02-19 |
BRPI0603389A (pt) | 2007-05-15 |
DE102005039590A1 (de) | 2007-02-22 |
CN101129295B (zh) | 2016-02-10 |
DE102005039590B4 (de) | 2008-05-21 |
JP5773557B2 (ja) | 2015-09-02 |
CN101129295A (zh) | 2008-02-27 |
US20070040151A1 (en) | 2007-02-22 |
ATE526937T1 (de) | 2011-10-15 |
EP1754465B1 (de) | 2011-10-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5773557B2 (ja) | 貯蔵安定性および酸系のための特別な適性 | |
JP6426729B2 (ja) | 会合及び凝集ナノ粒子の混合物を含有する硬化性歯科用組成物、これらの部分からなるキット、及びこれらの使用 | |
JP4828796B2 (ja) | イオン塩を含有する医用組成物 | |
KR101260525B1 (ko) | 다수의 산성 화합물을 포함하는 자체-접착성 조성물 | |
JP2690138B2 (ja) | 接着性組成物 | |
JP5271089B2 (ja) | 歯科用組成物及び多環式芳香族構成要素を有する開始剤系 | |
US20070100019A1 (en) | Catalyst system for dental compositions | |
BRPI0914427B1 (pt) | composição dental endurecivel | |
JP2010280630A (ja) | 歯科用プライマー及び歯科用接着材セット | |
JP2003532639A (ja) | 長い可使時間を有する歯科材料、キット及び方法 | |
US20150017596A1 (en) | Thermoplastic-based materials in orthodontic applications | |
JP6116480B2 (ja) | 反応性ペースト形成剤と重合可能な歯科用材料、硬化された歯科用材料およびこれらの使用 | |
JP6661673B2 (ja) | 酸中和樹脂及びその硬化性歯科用組成物 | |
JP5101072B2 (ja) | 歯科用組成物 | |
JP2009522279A (ja) | 水スカベンジャーを有する歯科用組成物 | |
JP4398254B2 (ja) | 歯科用接着剤 | |
JP7128114B2 (ja) | 分包型の歯科用セメント | |
CN111529410B (zh) | 具有改善的凝固性能的牙科材料 | |
CN113491636A (zh) | 以硅烷偶联剂配合量指标为特征的牙科用组合物 | |
US20100297588A1 (en) | Dental compositions with natural tooth fluorescence and methods | |
US20050054749A1 (en) | Dental adhesive composition | |
JPH0331684B2 (ja) | ||
JP2021508323A (ja) | 硬化前にステージ化された粘度を有する多成分形歯科用組成物 | |
JP6548661B2 (ja) | 歯科用材料を調製するためのモノマー混合物 | |
EP3542779B1 (en) | Dental composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20090414 |
|
RD04 | Notification of resignation of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7424 Effective date: 20101228 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120307 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20120605 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20120608 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20120704 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20120709 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20120803 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20120808 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120903 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20130111 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20150120 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20150220 |
|
RD13 | Notification of appointment of power of sub attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7433 Effective date: 20150318 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20150319 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20150319 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20150420 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20150630 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5773557 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |