http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-603370-A5

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B41M5-136
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B41M5-136
filingDate 1976-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4daf377b4832f05b0e6501c8f424d2d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f391cdc6574fbf4de8d04c13b4a5078
publicationDate 1978-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-603370-A5
titleOfInvention Carbonless copy system with chromogenic azo-methine cpd.
abstract Pressure-sensitive copying or recording material has a colour-forming system contg. azo-methin cpd(s). (I), as colour former, of the formula R2N-PHI-CH=N-A- (N=CH-PHI-NR2)n-1(H)2-n (where PHI is a p-phenylene gp. opt. with a halogen or 1-4C alkyl or alkoxy substit. The R gps. are each H, 1-4C alkyl, 2-5C cyanoalkyl or a benzyl or phenyl gp. opt. substd. by halogen or 1-4C alkyl or alkoxy, or each pair of R gps. is 4 or 5C alkylene.A is naphthyleneor phenylene substd. by (halo) phenoxy or 1-9C acylamino and opt. also by halogen 1-5C alkyl or 1-4C alkoxy, n = 1 or 2).(I) develop to intensive yellow to orange shades with excellent fastness to light and are very valuable in conjunction with other familiar colour formers for the prodn. of (marine) blue, grey or black shades.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5254522-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0453395-A1
priorityDate 1976-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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