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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B35-467
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B35-46
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B35-50
filingDate 1974-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bbb4cb6dddc596853cd682af81caecab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1f6043838426f9070b41389ee7eea8f
publicationDate 1975-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2416670-A1
titleOfInvention TRISAZO DYES
abstract The tris-azo dyes of formula (I) in the free acid from: (where A is the radical of an aromatic diazotisable component; B is the radical of an aromatic hydroxylated and/or aminated coupling component; n = 1 or 2; one X is OH and the other is NH2; Z is a radical of formula (II): in which Y is -SO2-NR; R is H, opt. substd.alkyl, or benzyl; R1 is H, Cl, Br, 1-4C alkyl, CN, COOH, MeO, EtO or NO2; R2 is H, Cl or 1-4C alkyl; R3 is H, Cl, Br, 1-4C alkyl, CN, MeO, EtOH, OH, COOH, NO2 or sulpho; R4 is H, Cl or Br; the azo gps. linked to Z are not in posn. 4:41 when both benzene rings are unsubstd. or monosubstd.), are used as green-black dyes for leather and also for natural or synthetic fibres contg. OH gps. e.g., cellulose, cotton, regenerated cellulose, wool, silk, nylon, and paper.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4623720-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9707168-A1
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priorityDate 1974-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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