http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-492764-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0ff16e899ce32685c9600075c1cc21
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-34
filingDate 1968-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b981c35683c07cd8360ccd51d0ff7c3a
publicationDate 1970-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-492764-A
titleOfInvention Process for the preparation of new water-insoluble monoazo compounds
abstract Azo pigments of formula where R1 is an aryl group, R2 is a naphthalene residue in which the azo-, OH and amide groups are in positions 1, 2 and 3, and R3 is a benzoxazolone, benzthiazolone or acridone residue bonded to the NH group in the 5 or 6 positions, are prepared by (a) condensing an acid halide of the formula R1-N=N-R2 COHal with an amine of the formula R3NH2 or (b) coupling a diazo compound or diazo-amino compound of an amine with the formula R1NH2 with a coupling component of formula R2CONHR3. The reactants are free from water-solubilising groups, such as sulphonic acid or COOH groups. The pigments are used in artificial silk, viscose, cellulose estehrs and esters, polyamides, polyurethanes polyesters, lacquers, natural and synthetic resins, rubber, casein, siloxanes, crayons, cosmetics and laminates.
priorityDate 1968-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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