JPH0481182B2

JPH0481182B2 -

Info

Publication number: JPH0481182B2
Authority: JP; Japan
Prior art keywords: bis; methane; tolyl; diethylaminophenyl; dimethylamino
Prior art date: 1983-03-31
Legal status : Expired - Lifetime

Application number

JP58053845A

Other languages

English (en)

Japanese (ja)

Other versions

JPS59180543A (ja

Inventor

Nobumasa Sasa

Yuzuru Sato

Tsugio Yamaoka

Current Assignee

Konica Minolta Inc

Original Assignee

Konica Minolta Inc

Priority date

1983-03-31

Filing date

1983-03-31

Publication date

1992-12-22

1983-03-31 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1983-03-31 Priority to JP5384583A priority Critical patent/JPS59180543A/ja

1984-10-13 Publication of JPS59180543A publication Critical patent/JPS59180543A/ja

1992-12-22 Publication of JPH0481182B2 publication Critical patent/JPH0481182B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 claims description 27
150000001875 compounds Chemical class 0.000 claims description 24
150000002896 organic halogen compounds Chemical class 0.000 claims description 8
125000001730 thiiranyl group Chemical group 0.000 claims description 5
-1 2-benzofuryl group Chemical group 0.000 description 35
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 21
238000000576 coating method Methods 0.000 description 16
230000035945 sensitivity Effects 0.000 description 16
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
239000002253 acid Substances 0.000 description 12
239000011248 coating agent Substances 0.000 description 12
OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 10
238000003860 storage Methods 0.000 description 10
150000004702 methyl esters Chemical class 0.000 description 9
239000000975 dye Substances 0.000 description 8
125000000217 alkyl group Chemical group 0.000 description 7
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 6
125000005843 halogen group Chemical group 0.000 description 6
239000000463 material Substances 0.000 description 6
238000000034 method Methods 0.000 description 6
229920005989 resin Polymers 0.000 description 6
239000011347 resin Substances 0.000 description 6
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
125000003118 aryl group Chemical group 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 4
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 4
150000001299 aldehydes Chemical class 0.000 description 4
229910052782 aluminium Inorganic materials 0.000 description 4
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
239000006224 matting agent Substances 0.000 description 4
239000000049 pigment Substances 0.000 description 4
239000003505 polymerization initiator Substances 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
239000000126 substance Substances 0.000 description 4
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 3
LWGYVQCNHZJBAX-UHFFFAOYSA-N 3-propylthiirene-2-carboxylic acid Chemical compound CCCC1=C(S1)C(=O)O LWGYVQCNHZJBAX-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
239000004793 Polystyrene Substances 0.000 description 3
229920002472 Starch Polymers 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
229910052786 argon Inorganic materials 0.000 description 3
229920006026 co-polymeric resin Polymers 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
229920001519 homopolymer Polymers 0.000 description 3
239000002245 particle Substances 0.000 description 3
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000004033 plastic Substances 0.000 description 3
229920002223 polystyrene Polymers 0.000 description 3
239000000243 solution Substances 0.000 description 3
235000019698 starch Nutrition 0.000 description 3
229920003002 synthetic resin Polymers 0.000 description 3
239000000057 synthetic resin Substances 0.000 description 3
TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 description 2
BHNHHSOHWZKFOX-UHFFFAOYSA-N 2-methyl-1H-indole Chemical compound C1=CC=C2NC(C)=CC2=C1 BHNHHSOHWZKFOX-UHFFFAOYSA-N 0.000 description 2
IKHXEJKFYFAGGF-UHFFFAOYSA-N 3-[3-[[3-(2-cyanoethyl)-2-(ethylamino)-6-methylphenyl]-[4-(dimethylamino)phenyl]methyl]-2-(ethylamino)-4-methylphenyl]propanenitrile Chemical compound CCNC1=C(CCC#N)C=CC(C)=C1C(C=1C(=C(CCC#N)C=CC=1C)NCC)C1=CC=C(N(C)C)C=C1 IKHXEJKFYFAGGF-UHFFFAOYSA-N 0.000 description 2
KZPPFENZDQQVRM-UHFFFAOYSA-N 3-[[5-(dimethylamino)-2-methylphenyl]-(2-fluorophenyl)methyl]-n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C(C(C=2C(=CC=C(C=2)N(C)C)C)C=2C(=CC=CC=2)F)=C1 KZPPFENZDQQVRM-UHFFFAOYSA-N 0.000 description 2
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
JYNVIMVQWVTAKD-UHFFFAOYSA-N 4-[(3-butoxyphenyl)-[4-(diethylamino)phenyl]methyl]-n,n-diethylaniline Chemical compound CCCCOC1=CC=CC(C(C=2C=CC(=CC=2)N(CC)CC)C=2C=CC(=CC=2)N(CC)CC)=C1 JYNVIMVQWVTAKD-UHFFFAOYSA-N 0.000 description 2
YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
108010010803 Gelatin Proteins 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
206010034972 Photosensitivity reaction Diseases 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 description 2
239000007983 Tris buffer Substances 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
238000007754 air knife coating Methods 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
150000004982 aromatic amines Chemical class 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
229920001727 cellulose butyrate Polymers 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
239000003086 colorant Substances 0.000 description 2
239000012954 diazonium Substances 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 2
MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 2
ALOUNLDAKADEEB-UHFFFAOYSA-N dimethyl sebacate Chemical compound COC(=O)CCCCCCCCC(=O)OC ALOUNLDAKADEEB-UHFFFAOYSA-N 0.000 description 2
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
208000028659 discharge Diseases 0.000 description 2
238000001035 drying Methods 0.000 description 2
125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 2
229920000159 gelatin Polymers 0.000 description 2
239000008273 gelatin Substances 0.000 description 2
235000019322 gelatine Nutrition 0.000 description 2
235000011852 gelatine desserts Nutrition 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
150000002391 heterocyclic compounds Chemical group 0.000 description 2
PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 2
RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
239000003999 initiator Substances 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000005259 measurement Methods 0.000 description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
229910052753 mercury Inorganic materials 0.000 description 2
DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
IQFYMOZHGUKAHQ-UHFFFAOYSA-N n-ethyl-2-[[2-(ethylamino)-5-methylphenyl]-(2-methoxyphenyl)methyl]-4-methylaniline Chemical compound CCNC1=CC=C(C)C=C1C(C=1C(=CC=C(C)C=1)NCC)C1=CC=CC=C1OC IQFYMOZHGUKAHQ-UHFFFAOYSA-N 0.000 description 2
RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
230000010355 oscillation Effects 0.000 description 2
230000036211 photosensitivity Effects 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
229920000139 polyethylene terephthalate Polymers 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
238000007639 printing Methods 0.000 description 2
SMUQFGGVLNAIOZ-UHFFFAOYSA-N quinaldine Chemical compound C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 2
KIWUVOGUEXMXSV-UHFFFAOYSA-N rhodanine Chemical compound O=C1CSC(=S)N1 KIWUVOGUEXMXSV-UHFFFAOYSA-N 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000008107 starch Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
238000012719 thermal polymerization Methods 0.000 description 2
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
229920006163 vinyl copolymer Polymers 0.000 description 2
NTNKNFHIAFDCSJ-UHFFFAOYSA-N (2-nitrophenyl) thiohypochlorite Chemical compound [O-][N+](=O)C1=CC=CC=C1SCl NTNKNFHIAFDCSJ-UHFFFAOYSA-N 0.000 description 1
LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
VNBOGBUTBBMQEA-UHFFFAOYSA-N (4-nitrophenyl)-[10-phenyl-2,8-bis(2-phenylethylamino)phenazin-5-yl]methanone Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)N1C2=CC=C(NCCC=3C=CC=CC=3)C=C2N(C=2C=CC=CC=2)C2=CC(NCCC=3C=CC=CC=3)=CC=C21 VNBOGBUTBBMQEA-UHFFFAOYSA-N 0.000 description 1
QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 description 1
POJPQMDDRCILHJ-UHFFFAOYSA-N 1,1,1,2,2,2-hexabromoethane Chemical compound BrC(Br)(Br)C(Br)(Br)Br POJPQMDDRCILHJ-UHFFFAOYSA-N 0.000 description 1
JUGRTVJQTFZHOM-UHFFFAOYSA-N 1,1,1-tribromo-2-methylpropan-2-ol Chemical compound CC(C)(O)C(Br)(Br)Br JUGRTVJQTFZHOM-UHFFFAOYSA-N 0.000 description 1
QXSZNDIIPUOQMB-UHFFFAOYSA-N 1,1,2,2-tetrabromoethane Chemical compound BrC(Br)C(Br)Br QXSZNDIIPUOQMB-UHFFFAOYSA-N 0.000 description 1
AFBQXBNIXGTXHL-UHFFFAOYSA-N 1,1-dichloroethene;2-methylidenebutanedioic acid;prop-2-enenitrile Chemical compound C=CC#N.ClC(Cl)=C.OC(=O)CC(=C)C(O)=O AFBQXBNIXGTXHL-UHFFFAOYSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
WWVBUEQYURYPKX-UHFFFAOYSA-N 1,2-dihydrophenazin-1-amine Chemical class C1=CC=C2N=C3C(N)CC=CC3=NC2=C1 WWVBUEQYURYPKX-UHFFFAOYSA-N 0.000 description 1
WDCYWAQPCXBPJA-UHFFFAOYSA-N 1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1 WDCYWAQPCXBPJA-UHFFFAOYSA-N 0.000 description 1
FWKURECHUUQQQJ-UHFFFAOYSA-N 1,4-bis(ethylamino)-2,3-dihydroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=C(NCC)CCC(NCC)=C3C(=O)C2=C1 FWKURECHUUQQQJ-UHFFFAOYSA-N 0.000 description 1
PWIBNXJNCSPLKW-UHFFFAOYSA-N 1,4-dianilino-2,3-dihydroanthracene-9,10-dione Chemical compound C=12C(=O)C3=CC=CC=C3C(=O)C2=C(NC=2C=CC=CC=2)CCC=1NC1=CC=CC=C1 PWIBNXJNCSPLKW-UHFFFAOYSA-N 0.000 description 1
VHKDRQQIBJZCPF-UHFFFAOYSA-N 1-(2-ethenoxyethoxy)naphthalene Chemical compound C1=CC=C2C(OCCOC=C)=CC=CC2=C1 VHKDRQQIBJZCPF-UHFFFAOYSA-N 0.000 description 1
BTSMHPNYPQWDGC-UHFFFAOYSA-N 1-(4-nitrophenyl)-2-phenylhydrazine Chemical compound C1=CC([N+](=O)[O-])=CC=C1NNC1=CC=CC=C1 BTSMHPNYPQWDGC-UHFFFAOYSA-N 0.000 description 1
JEOGFTYLESYHAM-UHFFFAOYSA-N 1-[3,7-bis(dimethylamino)phenothiazin-10-yl]ethanone Chemical compound C1=C(N(C)C)C=C2SC3=CC(N(C)C)=CC=C3N(C(C)=O)C2=C1 JEOGFTYLESYHAM-UHFFFAOYSA-N 0.000 description 1
IQKBMBWCUJRFFI-UHFFFAOYSA-N 1-amino-2,3-dihydroanthracene-9,10-dione Chemical class C1=CC=C2C(=O)C3=CCCC(N)=C3C(=O)C2=C1 IQKBMBWCUJRFFI-UHFFFAOYSA-N 0.000 description 1
AESUERRYMKWNNT-UHFFFAOYSA-N 1-ethyl-2-(3-quinolin-2-ylprop-2-enylidene)quinoline Chemical compound C1=CC2=CC=CC=C2N(CC)C1=CC=CC1=CC=C(C=CC=C2)C2=N1 AESUERRYMKWNNT-UHFFFAOYSA-N 0.000 description 1
UHHYXKFOBIODNU-UHFFFAOYSA-N 1-ethyl-2-(quinolin-4-ylmethylidene)quinoline Chemical compound C1=CC2=CC=CC=C2N(CC)C1=CC1=CC=NC2=CC=CC=C12 UHHYXKFOBIODNU-UHFFFAOYSA-N 0.000 description 1
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 1
AMKQRLOPSSMNEC-UHFFFAOYSA-N 1-naphthalen-2-yl-2-phenylhydrazine Chemical compound C=1C=C2C=CC=CC2=CC=1NNC1=CC=CC=C1 AMKQRLOPSSMNEC-UHFFFAOYSA-N 0.000 description 1
IXZRLXWDWGAGBH-UHFFFAOYSA-N 1-nitro-4-(tribromomethyl)benzene Chemical compound [O-][N+](=O)C1=CC=C(C(Br)(Br)Br)C=C1 IXZRLXWDWGAGBH-UHFFFAOYSA-N 0.000 description 1
FXSQXPLBHJAEKJ-UHFFFAOYSA-N 10-(2-chlorophenyl)-5h-phenazine-2,8-diamine Chemical compound C12=CC(N)=CC=C2NC2=CC=C(N)C=C2N1C1=CC=CC=C1Cl FXSQXPLBHJAEKJ-UHFFFAOYSA-N 0.000 description 1
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