http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0606953-A2

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filingDate 1994-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1101785886736821ea9f91b99e026efb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2492b923fa46951dac27d7a1d88319e
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de574e5d248e236f153289de51b38563
publicationDate 1994-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0606953-A2
titleOfInvention Image formation in color reversal materials using strong inhibitors
abstract An improved color reversal element comprising: na support having thereon at least two light-sensitive silver halide emulsion layers and a compound capable of releasing a development inhibitor, the element comprising a compound having the structural formula n n        CAR -(TIME) n -INH n n n wherein: n   CAR is a carrier moiety from which -(TIME) n -INH is released during color development; n   TIME is a timing group; nINH is comprised of a development inhibitor moiety selected from the group consisting of oxazole, thiazole, diazole, oxathiazole, triazole, thiatriazole, benzotriazole, tetrazole, benzimidazole, indazole, isoindazole, mercaptotriazole, mercaptothiadiazole, mercaptotetrazole, selenotetrazole, mercaptothiazole, selenobenzothiazole, mercaptobenzoxazole, selenobenzoxazole, mercaptobenzimidazole, mercaptobenzothiazole, selenobenzimidazole, benzodiazole, mercaptooxadiazole, or benzisodiazole, the INH having an inhibitor strength greater than 1 (one), and n   n is 0, 1 or 2.
priorityDate 1993-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID80533
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24478
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID253881

Total number of triples: 301.