http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1145655-A

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B45-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B35-03
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B35-03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B45-02
filingDate 1967-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1969-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1145655-A
titleOfInvention Azo dyestuffs and method for making same
abstract 1,145,655. Azo dyes containing a thiosulphate group. MARTIN-MARIETTA CORP. 5 April, 1967 [11 April, 1966], No. 15582/67. Addition to 1,083,165. Heading C4P. The invention comprises (a) azo dyestuffs of the formula wherein X is the #portion of an a-unsubstituted #-keto acid or ester; Y is H, halogen, CH 3 , C 2 H 5 , CH 3 O, C 2 H 5 O or the radical of a sulphonamide; Z is H, Na, K, or NH 4 ; R 1 is H, halogen, C 2 H 5 ,<SP> </SP>CH 3 O, C 2 H 5 O or phenoxy; E is a radical of the phenylene or naphthylene series; and in which the SSO 3 Z group is in m or p position to the N attached to the benzene nucleus; (b) 1: 1 Cu, Co, Cr, Ni or Fe, 1: 2 Cr, Co or Ni complexes of azo dyes of the formula in which the NHSO 2 group is located m or p to the azo group, R 2 is a metallizable group o to the azo group, R 3 is H, halogen, CH 3 or CH 3 O in m or p to the azo group, and in which the SSO 3 Z group is in m or p-position to the N attached to the benzene nucleus; (c) a metal complex resulting from the reaction of 1 mol. of a dye of formula with 2 mols. of a compound of formula and 2 atomic proportions of Co, Cr or Ni, said reactants being in solution; wherein J is the radical of a diazo compound having a metallizable substituent on an aromatic portion thereof; a ring C atom of which aromatic portion is linked to the C atom of the pyrazolone ring via an azo group of the radical of the diazo compound, and in which the metallizable substituent is located o to said azo group; (d) an azo dye of the formula and (e) an azo dye of the formula The dyes may be obtained by diazotizing the appropriate amines and coupling with the appropriate pyrazolone coupling component and when required, metallizing the resulting azo dye. Examples are given for the production of the dyes.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4623720-A
priorityDate 1964-07-16-04:00^^<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: 24.