GB830797A - New colour couplers for use in colour photography - Google Patents
New colour couplers for use in colour photographyInfo
- Publication number
- GB830797A GB830797A GB9113/57A GB911357A GB830797A GB 830797 A GB830797 A GB 830797A GB 9113/57 A GB9113/57 A GB 9113/57A GB 911357 A GB911357 A GB 911357A GB 830797 A GB830797 A GB 830797A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- phenyl
- pyrazolone
- formula
- reacting
- 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.)
- Expired
Links
- -1 aralkyl radical Chemical group 0.000 abstract 9
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 150000008064 anhydrides Chemical class 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 2
- PVKNQGWSRAGMNM-UHFFFAOYSA-N 5-amino-2-phenyl-1h-pyrazol-3-one Chemical compound N1C(N)=CC(=O)N1C1=CC=CC=C1 PVKNQGWSRAGMNM-UHFFFAOYSA-N 0.000 abstract 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 239000012024 dehydrating agents Substances 0.000 abstract 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 2
- 239000011976 maleic acid Substances 0.000 abstract 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 2
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 abstract 1
- FLUYDOVOMDZUEV-UHFFFAOYSA-N 2-(4-nitrophenoxy)acetyl chloride Chemical compound [O-][N+](=O)C1=CC=C(OCC(Cl)=O)C=C1 FLUYDOVOMDZUEV-UHFFFAOYSA-N 0.000 abstract 1
- FYXZTVPBFJQFBO-UHFFFAOYSA-N 2-(4-nitrophenyl)acetyl chloride Chemical compound [O-][N+](=O)C1=CC=C(CC(Cl)=O)C=C1 FYXZTVPBFJQFBO-UHFFFAOYSA-N 0.000 abstract 1
- QDGJHZNOQSIFAT-UHFFFAOYSA-N 2-amino-4-chloro-5-methylphenol Chemical compound CC1=CC(O)=C(N)C=C1Cl QDGJHZNOQSIFAT-UHFFFAOYSA-N 0.000 abstract 1
- QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical class C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 abstract 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 abstract 1
- ZBIBQNVRTVLOHQ-UHFFFAOYSA-N 5-aminonaphthalen-1-ol Chemical compound C1=CC=C2C(N)=CC=CC2=C1O ZBIBQNVRTVLOHQ-UHFFFAOYSA-N 0.000 abstract 1
- CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000008065 acid anhydrides Chemical class 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 150000005840 aryl radicals Chemical group 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 abstract 1
- 125000004185 ester group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- JYYDHGMTXHCSKZ-UHFFFAOYSA-N ethyl 4-hydrazinylbenzoate Chemical compound CCOC(=O)C1=CC=C(NN)C=C1 JYYDHGMTXHCSKZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 abstract 1
- 229910000105 potassium hydride Inorganic materials 0.000 abstract 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical group O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/3212—Couplers characterised by a group not in coupling site, e.g. ballast group, as far as the coupling rest is not specific
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
- C07D231/52—Oxygen atom in position 3 and nitrogen atom in position 5, or vice versa
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE565852D BE565852A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1957-03-20 | ||
GB9113/57A GB830797A (en) | 1957-03-20 | 1957-03-20 | New colour couplers for use in colour photography |
FR1202940D FR1202940A (fr) | 1957-03-20 | 1958-03-19 | Nouveaux copulants chromogènes applicables dans la photographie en couleurs |
DEJ19128A DE1115129B (de) | 1957-03-20 | 1958-03-20 | Farbkuppler enthaltende farbphotographische Schicht |
US52354A US3133815A (en) | 1957-03-20 | 1960-08-29 | Color photographic materials and processes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9113/57A GB830797A (en) | 1957-03-20 | 1957-03-20 | New colour couplers for use in colour photography |
Publications (1)
Publication Number | Publication Date |
---|---|
GB830797A true GB830797A (en) | 1960-03-23 |
Family
ID=9865609
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9113/57A Expired GB830797A (en) | 1957-03-20 | 1957-03-20 | New colour couplers for use in colour photography |
Country Status (5)
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003106445A1 (en) * | 2002-06-12 | 2003-12-24 | Qsi Pharma A/S | Compounds and methods for controlling bacterial virulence |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3515557A (en) * | 1965-04-12 | 1970-06-02 | Du Pont | Photographic color film and process of making same |
US5945268A (en) * | 1996-08-26 | 1999-08-31 | Konica Corporation | Silver halide color photographic light-sensitive material |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2964402A (en) * | 1951-10-03 | 1960-12-13 | Gevaert Photo Prod Nv | Mono-acetyl indazolone color couplers |
-
0
- BE BE565852D patent/BE565852A/xx unknown
-
1957
- 1957-03-20 GB GB9113/57A patent/GB830797A/en not_active Expired
-
1958
- 1958-03-19 FR FR1202940D patent/FR1202940A/fr not_active Expired
- 1958-03-20 DE DEJ19128A patent/DE1115129B/de active Pending
-
1960
- 1960-08-29 US US52354A patent/US3133815A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003106445A1 (en) * | 2002-06-12 | 2003-12-24 | Qsi Pharma A/S | Compounds and methods for controlling bacterial virulence |
Also Published As
Publication number | Publication date |
---|---|
DE1115129B (de) | 1961-10-12 |
BE565852A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
FR1202940A (fr) | 1960-01-14 |
US3133815A (en) | 1964-05-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB937621A (en) | Improvements in colour photography and in colour-forming phenylazo-pyrazolones therefor | |
GB768821A (en) | Novel products of the amino-piperidine-2, 6-dione series | |
GB830797A (en) | New colour couplers for use in colour photography | |
GB585780A (en) | Improvements in or relating to the production of pyrazolones | |
GB975248A (en) | Novel colour couplers and their use in colour photography | |
GB841300A (en) | Improvements in or relating to colour photography | |
GB1043505A (en) | Water-soluble disazo-dyestuffs and process for preparing them | |
GB1132314A (en) | Triazolyl stilbene derivatives and their use as brightening agents | |
GB858564A (en) | New colour couplers | |
US3236861A (en) | Organic imido compounds | |
GB1004075A (en) | Improvements in or relating to colour couplers and to their production and use in colour photography | |
GB858482A (en) | New colour couplers | |
GB1076635A (en) | Processes for the manufacture of disazo pigments | |
GB949944A (en) | Amide colour couplers | |
GB977472A (en) | New monoazo compounds containing halogeno-triazinylamino groups | |
GB890305A (en) | Amide colour couplers for colour photography | |
GB689977A (en) | Manufacture of condensation products | |
GB754660A (en) | New pyrazolones and process for their manufacture | |
GB944843A (en) | Process for the manufacture of 2-(2-aminoaryl)-4:5-arylene-1:2:3-triazole-1-oxides | |
US3470191A (en) | Process for the preparation of 3-arylamino-2-pyrazolin-5-one | |
GB868474A (en) | Improvements relating to monoazo-pyrazole dyestuffs and their use | |
GB1122905A (en) | Developing process for colour photography | |
GB1098356A (en) | Method for the preparation of azabicycloheptane derivatives | |
GB1307406A (en) | 1,2,4-triazolyl-1-derivatives of the stilbene and bis-styryl-benzene series process for their manufacture and their use as optical brighteners | |
GB957414A (en) | Benzene monoazo dyestuffs |