http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0074589-A2

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D21H21-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06P1-41
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B43-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B44-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B44-02
filingDate 1982-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2109c37b2f96b69df26c8a995be51ab2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d3d0065cd79f16213229825bfea2cf10
publicationDate 1983-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0074589-A2
titleOfInvention Triazine dyes, their preparation and their use
abstract U und W unabhängig voneinander Reste der Formelnn A ein von anionischen Gruppen freier bifunktioneller aromatischer Rest, Q eine direkte Bindung oder ein Brückenglied, X ein Rest der Formel -COCH 3 , -CN, -COOCH 3 , -COOC 2 H 5 , -CONH 2 , -COC 6 H 5 oder -CON(R 3 )-Y-N(R 5 R 6 R 7 ) (+) An (-), Y ein zweiwertiges Brückenglied oder eine direkte Bindung, R 1 und R 2 unabhängig voneinander Wasserstoff oder ein nichtionischer Substituent, R 3 Wasserstoff, C 1 -C 4 -Alkyl oder β- oder y-C 2 -C 4 -Hydroxyalkyl, R 5 - R 7 unabhängig voneinander Wasserstoff, C 1 -C 4 -Alkyl, oder C 2 -C 4 -Alkyl, das durch Hydroxy, Amino, C 1 -C 4 -Alkylamino, Di-C,-C 4 -alkyl-amino oder Tri-C 1 -C 4 - alkyl-ammonium substituiert ist, Phenyl oder Benzyl sind, oder R 5 und R 6 zusammen mit dem Stickstoff einen gegebenenfalls substituierten fünf- oder sechsgliedrigen Heterocyclus oder Y, R 3 und R 5 zusammen mit den jeweiligen Stickstoffatomen einen Piperazinring bilden oder R 5 , R 6 und R 7 zusammen mit dem Stickstoff ein gegebenenfalls substituiertes Pyridinum bilden, und An (-) ein Anion ist, nsind zum Färben synthetischer und natürlicher Materialien, insbesondere Papier geeignet.Dyes of the formula wherein U and W independently of each other residues of the formulas A is a bifunctional aromatic radical free from anionic groups, Q a direct bond or a bridge link, X is a radical of the formula -COCH 3 , -CN, -COOCH 3 , -COOC 2 H 5 , -CONH 2 , -COC 6 H 5 or -CON (R 3 ) -YN (R 5 R 6 R 7 ) (+ ) At (-), Y is a divalent bridge link or a direct bond, R 1 and R 2 independently of one another are hydrogen or a nonionic substituent, R 3 is hydrogen, C 1 -C 4 -alkyl or β- or yC 2 -C 4 -hydroxyalkyl, R 5 - R 7 independently of one another are hydrogen, C 1 -C 4 alkyl, or C 2 -C 4 alkyl, which is substituted by hydroxy, amino, C 1 -C 4 alkylamino, di-C, -C 4 alkyl- amino or tri-C 1 -C 4 -alkyl-ammonium is substituted, are phenyl or benzyl, or R 5 and R 6 together with the nitrogen are an optionally substituted five- or six-membered heterocycle or Y, R 3 and R 5 together with the respective nitrogen atoms form a piperazine ring or R 5 , R 6 and R 7 together with the nitrogen form an optionally substituted pyridinum, and An (-) is an anion are suitable for dyeing synthetic and natural materials, especially paper.
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priorityDate 1981-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419517283
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID155594
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421786463
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22833652
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128783572
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128592340
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419515546
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420298565
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128782965
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226472070
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6163
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420869427
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID61055
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129372882
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128334652
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128401944
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21379
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128385765
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12855
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12661
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11998
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129754721
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69917
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408765155
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421981911
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559059
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419502152
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7943
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5942
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6323
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424592624
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127788221
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419551550
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8117
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415803598
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7777
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226403877
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419547105

Total number of triples: 340.