GB519208A - Improvements in or relating to colour photography - Google Patents
Improvements in or relating to colour photographyInfo
- Publication number
- GB519208A GB519208A GB2716638A GB2716638A GB519208A GB 519208 A GB519208 A GB 519208A GB 2716638 A GB2716638 A GB 2716638A GB 2716638 A GB2716638 A GB 2716638A GB 519208 A GB519208 A GB 519208A
- Authority
- GB
- United Kingdom
- Prior art keywords
- groups
- amino
- substituted
- hydroxy
- atoms
- 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 naphthathiazole Chemical compound 0.000 abstract 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 4
- 229910052801 chlorine Inorganic materials 0.000 abstract 4
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine group Chemical group N1=CCC2=CC=CC=C12 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 3
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical group C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical group N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 abstract 2
- 239000000460 chlorine Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000005429 oxyalkyl group Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- ODIRBFFBCSTPTO-UHFFFAOYSA-N 1,3-selenazole Chemical group C1=C[se]C=N1 ODIRBFFBCSTPTO-UHFFFAOYSA-N 0.000 abstract 1
- BGDWGIMWXKYYOG-UHFFFAOYSA-N 1-hydroxynaphthalene-2-carbonyl chloride Chemical compound C1=CC=C2C(O)=C(C(Cl)=O)C=CC2=C1 BGDWGIMWXKYYOG-UHFFFAOYSA-N 0.000 abstract 1
- LQERUHGIVUXADN-UHFFFAOYSA-N 1-imino-2,3-dihydro-1,3-benzothiazole Chemical compound C1=CC=C2S(=N)CNC2=C1 LQERUHGIVUXADN-UHFFFAOYSA-N 0.000 abstract 1
- LEDIQKJQBDKDOG-UHFFFAOYSA-N 1-methyl-3,4-dihydroquinolin-2-imine Chemical compound N=C1N(C2=CC=CC=C2CC1)C LEDIQKJQBDKDOG-UHFFFAOYSA-N 0.000 abstract 1
- OIWIYLWZIIJNHU-UHFFFAOYSA-N 1-sulfanylpyrazole Chemical compound SN1C=CC=N1 OIWIYLWZIIJNHU-UHFFFAOYSA-N 0.000 abstract 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical group C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 abstract 1
- SIXYIEWSUKAOEN-UHFFFAOYSA-N 3-aminobenzaldehyde Chemical compound NC1=CC=CC(C=O)=C1 SIXYIEWSUKAOEN-UHFFFAOYSA-N 0.000 abstract 1
- MVVFUAACPKXXKJ-UHFFFAOYSA-N 4,5-dihydro-1,3-selenazole Chemical group C1CN=C[Se]1 MVVFUAACPKXXKJ-UHFFFAOYSA-N 0.000 abstract 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 abstract 1
- 239000005711 Benzoic acid Substances 0.000 abstract 1
- DQQUBOUBXUDICH-UHFFFAOYSA-N CCOC(C=C1)=CC(N=C2)=C1[S+]2N Chemical compound CCOC(C=C1)=CC(N=C2)=C1[S+]2N DQQUBOUBXUDICH-UHFFFAOYSA-N 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 abstract 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical group C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 abstract 1
- 235000010233 benzoic acid Nutrition 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Chemical group 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- DADSZOFTIIETSV-UHFFFAOYSA-N n,n-dichloroaniline Chemical compound ClN(Cl)C1=CC=CC=C1 DADSZOFTIIETSV-UHFFFAOYSA-N 0.000 abstract 1
- XNBILEFKIHECKR-UHFFFAOYSA-N n-bromo-n-chloroaniline Chemical compound ClN(Br)C1=CC=CC=C1 XNBILEFKIHECKR-UHFFFAOYSA-N 0.000 abstract 1
- KUDPGZONDFORKU-UHFFFAOYSA-N n-chloroaniline Chemical compound ClNC1=CC=CC=C1 KUDPGZONDFORKU-UHFFFAOYSA-N 0.000 abstract 1
- 150000002790 naphthalenes Chemical class 0.000 abstract 1
- FHZUMJAAGNDUKE-UHFFFAOYSA-N naphtho[2,3-e][1,3]benzothiazole Chemical compound C1=CC=C2C=C3C(N=CS4)=C4C=CC3=CC2=C1 FHZUMJAAGNDUKE-UHFFFAOYSA-N 0.000 abstract 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 abstract 1
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Chemical group COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 abstract 1
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical group C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 abstract 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical group C1CN=CS1 CBDKQYKMCICBOF-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
- G03C7/34—Couplers containing phenols
- G03C7/344—Naphtholic couplers
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Cosmetics (AREA)
Abstract
519,208. 1 - Hydroxy - 2 - napthoylanhilides. KENDALL, J. D.,' and COLLINS, R. B. Sept. 17, 1938, No. 27166. Drawings to Specification. [Class 2 (iii)] [Also in Group XX] Compound of the general formula where R is a phenyl group substituted by one chlorine atom, two chlorine atoms, one bromine atom, two bromine atoms, or one chlorine atom and one bromine atom,.and where X is hydrogen, chlorine, or bromine, are prepared by condensing a 1-hydroxy-2-naphthoylhalide (which may be unsubstituted or substituted in the 4- position by a chlorine or bromine atom) with a chloraniline, dichloraniline, bromaniline, dibromaniline, or chlorbromaniline. The compounds prepared from o- and p-chlor-and bromanilines and 2:4-dichloraniline are referred to. The Provisional Specification refers to colour formers of the general formula while R1 and R2represent either the same or different atoms or groups consisting of hydrogen atoms, alky groups such as methyl, ethyl, or propyl, aryl groups such as phenyl, aralkyl groups such as benzyl, heterocyclic groups such as thiazole, thiazoline, oxazole, oxazoline, selenazole, selenazoline, pyridine, quinoline, indolenine, diazole or diazine such as pyrimidine, thiodiazole, or quinazoline, benzthiazole, naphthathiazole, and anthrathiazole, or a single cyclic grouping such as piperidine, pyrazole, indole, or N-alkyldihydrobenzthiazole and X represents hydrogen or a halogen atom. The groups R1 and R2may be substituted by halogen atoms or amino, substituted, amino, nitro, hydroxy, alkoxy, or oxyalkyl groups. The naphthalene nucleus may be substituted in any of the 3-, 5-, 6-, 7-, or 8- positions with halogen atoms or alkyl, aryl, amino, substituted amino, nitro, hydroxy, alkoxy, carbalkoxy, or oxyalkyl groups. 1-hydroxy-2-naphthoylchloride may be condensed with ammonia, aniline, monomethylaniline, p-nitroaniline, oc- or #-naphthylamine, ethyloc-naphthylamine, o- or p-anisidine, p-aminophenol, p-amino-. benzoic acid, 2:6-dibrom-4-aminophenol, maminoacetophenone, m - aminobenzaldehyde, ethyl - p -aminobenzoate, 1 - amino - 5 -ethoxybenzthiazole, 1-iminodihydrobenzthiazole, or 2-imino-1-methyl-dihydroquinoline.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2716638A GB519208A (en) | 1938-09-17 | 1938-09-17 | Improvements in or relating to colour photography |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2716638A GB519208A (en) | 1938-09-17 | 1938-09-17 | Improvements in or relating to colour photography |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB519208A true GB519208A (en) | 1940-03-19 |
Family
ID=10255274
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2716638A Expired GB519208A (en) | 1938-09-17 | 1938-09-17 | Improvements in or relating to colour photography |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB519208A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2521908A (en) * | 1947-03-13 | 1950-09-12 | Eastman Kodak Co | 1-hydroxy-2-naphthamide colored couplers |
| US3005709A (en) * | 1958-01-13 | 1961-10-24 | Gen Aniline & Film Corp | Photographic couplers containing acylamino groups |
| US4178183A (en) * | 1978-07-27 | 1979-12-11 | Eastman Kodak Company | Thiazolyl coupler compositions and photographic elements suited to forming integral sound tracks |
| US4208210A (en) * | 1974-12-19 | 1980-06-17 | Fuji Photo Film Co., Ltd. | Process for forming an optical soundtrack |
| US5030544A (en) * | 1984-09-28 | 1991-07-09 | Agfa-Gevaert, N.V. | Photographic elements comprising thiazolyl couplers capable of forming infrared-absorbing dyes for integral sound track |
-
1938
- 1938-09-17 GB GB2716638A patent/GB519208A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2521908A (en) * | 1947-03-13 | 1950-09-12 | Eastman Kodak Co | 1-hydroxy-2-naphthamide colored couplers |
| US3005709A (en) * | 1958-01-13 | 1961-10-24 | Gen Aniline & Film Corp | Photographic couplers containing acylamino groups |
| US4208210A (en) * | 1974-12-19 | 1980-06-17 | Fuji Photo Film Co., Ltd. | Process for forming an optical soundtrack |
| US4178183A (en) * | 1978-07-27 | 1979-12-11 | Eastman Kodak Company | Thiazolyl coupler compositions and photographic elements suited to forming integral sound tracks |
| US5030544A (en) * | 1984-09-28 | 1991-07-09 | Agfa-Gevaert, N.V. | Photographic elements comprising thiazolyl couplers capable of forming infrared-absorbing dyes for integral sound track |
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