http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5933254-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_be92719b856db86c092cc233e9512ca2
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C245-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B56-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-91
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03G5-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-80
filingDate 1982-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e9a654f2473e8e9235d2690de0d8a65
publicationDate 1984-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5933254-A
titleOfInvention Novel tetrazonium salt compound, novel disazo compound and its preparation
abstract NEW MATERIAL:A tetrazonium salt compound shown by the formula I (Y is anionic functional group) or a disazo compound shown by the formula II (X is aromatic ring, or hetero ring; Ar is aromatic ring, or hetero ring). n USE: A tetrazonium salt compound is useful as an intermediate for disazo compounds. The disazo compounds are useful as photoelectric materials for sensitized materials for electrophotography, especially as charge-generating materials. Since a laminate type sensitized material has a photosensitive wavelength band in about 450W600nm at short wave side of visible light range, it has improved reproducibility of reprography image of red manuscript. n PROCESS: 1,5-Diaminoanthraquinone shown by the formula III is diazotized with sodium nitrite in an inorganic acid to give a tetrazonium salt shown by the formula I . This compound is reacted with a coupler shown by the formula IV at -10W40°C, to give a disazo compound shown by the formula II. n COPYRIGHT: (C)1984,JPO&Japio
priorityDate 1982-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 21.