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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C7-384
filingDate 1996-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6ccafeba85701b74c6b1e794385f7d6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2696b0cf67e9006821488f350845b416
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42bf374502975eb2e9954ef1eaccd421
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8e76f5fc04a502a4f86fb5175c6403f7
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20f2e4edbe58f1ff980e8dda6b4a0dcf
publicationDate 1997-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-2314327-A
titleOfInvention Pyrazolone image dye-forming couplers
abstract An image magenta-forming coupler of formula (I):- * space * wherein X is H or a coupling-off group, R is H; or R, R 1 and R 2 are the same or different and are coupler-modifying functional groups; or R 1 and R 2 taken together with the nitrogen atom and the carbonyl group form a 5-10 membered heterocyclic ring which may contain one or more further heteroatoms selected from N, O and S, said heterocyclic ring being unsubstituted or substituted with one or more coupler-modifying functional groups, either with or without another main image dye-forming coupler,is used to provide an image of enhanced stability to exposure to light. The couplers (I) are novel compounds provided that (a) the moiety N(R 1 )COR 2 is not a carbamate,ureide or imide and (6) R 1 and R 2 are not both phenyl or substituted phenyl.
priorityDate 1996-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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