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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bb0a7b16a31bf7bc8b903ed8b717aab6
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03C7-344
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C7-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-90
filingDate 1989-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14d69aef9c2f09919eed699e57fe9e82
publicationDate 1991-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5015565-A
titleOfInvention Color photographic recording material
abstract A color photographic recording material comprising at least one silver halide emulsion layer and a naphtholic cyan coupler corresponding to formula I <IMAGE> (I) in which Q is a 5-, 6- or 7-membered heterocyclic radical; S is a substituent which, in the 6-position of the naphthol ring, can form a fused heterocyclic ring with Y; l is 0, 1, 2 or 3; X represents H or a group releasable during color coupling which is capable of forming a fused heterocyclic ring with Y; Y represents -Z-R1 or -NH-R2; Z represents -O-, -S(O)m- or -SO2-NH-; m is 0, 1 or 2; R1 represents H, CF3, alkyl, aryl or a heterocyclic radical; R2 represents H or a monofunctional radical containing at least one carbon atom which is capable of forming a fused heterocyclic ring with X or with S (in the 6-position of the naphthol ring), gives a cyan dye image on chromogenic development with desired absorption at approximately 700 nm, good dark fading stability and high reproducibility, even where spent bleaching baths are used.
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priorityDate 1988-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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