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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5d9f3ca41550d315642580237250c5b0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03C7-3835
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C7-38
filingDate 1993-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9e9cea5b88f306eda3c61728cadcae9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_063c5f9e7308e645e27bfa113fd540df
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df2d1547bc73ca909bc511b773b7f4f9
publicationDate 1993-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0558144-A1
titleOfInvention Photographic material and process comprising a pyrazolotriazole coupler
abstract Novel pyrazolotriazole couplers containing a ballast group of formula (I):n n wherein: n   n is 0, 1 or 2; n   R² is hydrogen or a substituent; n   B is hydrogen or a substituent; n   L' is O, S, Se, Te, Si(R⁵)₂, NR⁵, PR⁵, P(O)(R⁵)₂ or NR⁵SO₂, wherein R⁵ is hydrogen, alkyl or aryl; and n   R³ is a substituent, nare useful in photographic materials and processes. The couplers exhibit increased coupling activity, and provide formation of dyes having improved maximum magenta image dye density, contrast, and development speed when employed in color photographic materials and processes.
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priorityDate 1992-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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