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Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B31-047
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filingDate 1971-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1973-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1316724-A
titleOfInvention Disazo dyestuffs
abstract 1316724 Disazo dyes BAYER AG 19 April 1971 [14 Feb 1970 10 Oct 1970] 21629/71 Heading C4P The invention comprises disazo dyes of formula wherein W is a radical of formula In the above formulae R 1 is H or an optionally substituted alkyl or phenyl group; R 2 and R 3 independently represent H, halogen, an optionally substituted alkyl or alkoxy group or an acylamino group; R 4 is H, halogen or optionally substituted alkyl, alkoxy or an acylamine group; R 5 is H or an optionally substituted alkyl or alkoxy group; R 6 and R 7 independently represent hydrogen, hydroxy, cyano, halogen, acyloxy, alkoxycarbonyl, or an optionally substituted phenyl group; X is a C 1 -C 4 alkylene radical; R 8 is an unsubstituted alkyl, phenyl or 2-naphthyl or 4-biphenylyl group; R 9 is H, C 1 -C 6 alkyl group optionally substituted by a nitrile, carbamoyl or carboxyl group; R 10 is a substituent and n is 0, 1 or 2. The dyes are obtained by diazotizing a monoazo dyestuff of formula and coupling it with the required amine or indole. The monoazo dyes of Formula IV are obtained by coupling a diazotized aniline sulphonic acid with a coupling component of formula where Z represents a radical which may be split off by hydrolysis, e.g. sulphoalkylene a sulphonic acid. The group -NHZ is converted to an NH 2 prior to diazotization of the aminomonoazo compound. The dyes give red shades on synthetic fibre materials especially polyamides, e.g. poly #-caprolactam and condensate products of adipic acid and hexamethylene diamine.
priorityDate 1970-02-14-04:00^^<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: 38.