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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03C7-384
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C7-384
filingDate 1967-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1971-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de945f93d6f396564c6e9130f36adcc2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bda346f1708d39a5587fdf9f9ce9ba5e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e20b317d270ea764b0bb4e20e6cbb26
publicationDate 1971-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3563745-A
titleOfInvention Silver halide photographic materials containing 1-arylmethyl-2-pyrazolin-5-one color couplers
abstract COLORLESS MAGENTA FORMING COLOR COUPLERS OF THE 2PYRAZOLIN-5-ONE TYPE HAVING FORMULA: 1-(AR-CH2-),3-(R-CO-HN-)-2-PYRAZOLIN-5-ONE WHEREIN: AR REPRESENTS AN ARYL GROUP, AND R REPRESENTS AN ALKYL RADICAL, AN ARYL RADICAL, AN ARALKYL RADICAL, AN ALKOXY RADICAL, IN ARYLOXY RADICAL, AN ARALKYLOXY RADICAL, AN ALKYLAMINO RADICAL AN ARYLAMINO RADICAL OR AN ANALKYLAMINO RADICAL ARE DESCRIBED. THESE COLOR COUPLERS HAVE IMPROVED STABILITY WHEN STORED IN HUMID AND WARM ATMOSPHERES AND THE WHITE IMAGE AREAS DO NOT UNDERGO DISCOLORATION.
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priorityDate 1966-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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