http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0229339-A2

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filingDate 1986-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2eed567c73d341088fac93bf12632a2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01c36d15627e8f979f922a58d5726c25
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41a4e7996e962873f3421bdc54c9e77c
publicationDate 1987-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0229339-A2
titleOfInvention Water soluble triphene dioxazine compounds, their starting compounds containing sulphonyl groups, process for their preparation and use of the triphene dioxazines as dyestuffs
abstract Water-soluble triphendioxazine compounds with fiber-reactive dye properties and the general formula (1) in which mean: T is optionally substituted alkyl of 1 to 6 carbon atoms, with the exception of ethyl substituted in the β-position by an alkaline eliminable substituent, the alkyl being -O-, -S-, -NH- and -N (Rʹ) - with Rʹ may be interrupted, optionally substituted alkyl of 1 to 6 carbon atoms, or is optionally substituted aryl, B is -O-, -S-, -NH- or -N (Rʹʹ) - alkyl optionally substituted with Rʹʹ, W is a pontic or W and B together form a direct bond, R is hydrogen or a substituent, R * is hydrogen or a substituent or R * and W, if W contains an amino group, or part of W together with the nitrogen atoms form the remainder of a heterocycle, A is a non-heterocyclic fiber-reactive group or a 2-halogeno-s-triazin-6-yl radical which is in the 4-position by halogen or an optionally sub substituted amino group, which may also contain a fiber-reactive group, or is substituted by a heterocyclic radical or by another halogenotriazinyl radical connected via an amino radical as a bridge member, X¹ and X² are each hydrogen, halogen, cycloalkyl, aralkoxy, alkoxy, aryloxy, alkyl, aryl, aralkyl, cyano, carboxy, carbalkoxy, arylamino, carbamoyl and by alkyl, mono- or disubstituted carbamoyl or arylcarbamoyl, alkanoylamino or aroylamino, the Aryl radicals can each be substituted; of the sulfo and sulfato groups, the molecule contains at least one of these groups, furthermore precursors of the formulas with B * equal to -NH- or -N (Rʹʹ) - and R, R *, W and T of the above meanings.n n n The triphendioxazine compounds are used primarily for dyeing wool and synthetic polyamide fibers and in particular cellulose fibers using the application and fixing methods which are customary for fiber-reactive dyes.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0448815-A1
priorityDate 1985-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128512531
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226457968
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7965
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414867647
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421275256
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21285181
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420679739
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11228886
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128271569
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135867566
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21285191
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11772269

Total number of triples: 619.