http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0000346-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-650994 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D241-44 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-29 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06L3-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B23-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6509 |
| filingDate | 1978-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_246a4085e6e39bc4aa3dbcb2f09f95f7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02932e6cdc2102f1370a41d528d29743 |
| publicationDate | 1979-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0000346-A1 |
| titleOfInvention | Quinoxaline compounds, process for their manufacture and their use as brighteners for organic materials, and the materials brightened therewith |
| abstract | X und Y Wasserstoff, Halogen, Alkyl, Aralkyl, Alkenyl, Hydroxy, Amino, Alkoxy, Arafkoxy, Cycloatkoxy, Aryloxy, Alkylmercapto, Alkylamino, Dialkylamino, Morpholino, Piperidino, Piperazino, Pyrrolidino, Acylamino oder Arylamino, Q Wasserstoff, Pyrazol-1-yl, Oxazol-2-yl, Benzoxazol-2-yl, Naphthoxazol-2-yl, 1,2,4-Oxadiazol-5-yl, 1,3,4-Oxadi- azol-2-yl, Isoxazol-3-yl, Isoxazol-5-yl, Thiazol-2-yl, Benz- thiazol-2-yl, 1,3,4-Thiadiazol-2-yl, Imidazol-2-yl, Benzimidazol-2-yl, 1,2,3-Triazol-2-yl, 1,2,3-Triazol-4-yl, 1,2,4-Triazol-3-yl, 1,2,4-Triazol-5-yl, 1,3,5-Triazin-2-yl, 2H-Benzotriazol-2-yl, 2H-Naphthotriazol-2-yl, 1,2,3,4-Tetrazol-5-yl, 1,2,3,4-Tetrazol-1-yl, Benzo[b]-furan-2-yl, Naphtho[2,1-b]-furan-2-yl, Benzo[b]-thiophon-2-yl, Naphtho[2,1-b]-thiophen-2-yl, Pyrimidin-2-yl, Pyridin-2-yl, Chinazolin-4-yl oder China- zolin-2-yl, und - für den Fall, dass n = 0 - auch Naphthyl, Stilben-4-yl, Benzo[b]-furan-6-yl, Dibenzofuran-3-yl, Di- benzofuran-2-yl, Chinoxalin-5-yl, Chinazolin-6-yl oder 2H-Benzotriazol-5-yl und n 0, 1 oder 2 bedeuten, wobei die Substituenten X, Y, Q und die übrigen cyclischen Reste durch für Weisstöner übliche nicht-chromophore Substituenten weiter substituiert sein können, neignen sich zum Weisstönen der verschiedensten synthetischen, halbsynthetischen und natürlichen organischen hochmolekularen Materialien.Fluorescent dyes of the formula wherein X and Y are hydrogen, halogen, alkyl, aralkyl, alkenyl, hydroxy, amino, alkoxy, arafkoxy, cycloatkoxy, aryloxy, alkylmercapto, alkylamino, dialkylamino, morpholino, piperidino, piperazino, pyrrolidino, acylamino or arylamino, Q is hydrogen, pyrazol-1-yl, oxazol-2-yl, benzoxazol-2-yl, naphthoxazol-2-yl, 1,2,4-oxadiazol-5-yl, 1,3,4-oxadiazol-2 -yl, isoxazol-3-yl, isoxazol-5-yl, thiazol-2-yl, benzothiazol-2-yl, 1,3,4-thiadiazol-2-yl, imidazol-2-yl, benzimidazol-2 -yl, 1,2,3-triazol-2-yl, 1,2,3-triazol-4-yl, 1,2,4-triazol-3-yl, 1,2,4-triazol-5-yl , 1,3,5-triazin-2-yl, 2H-benzotriazol-2-yl, 2H-naphthotriazol-2-yl, 1,2,3,4-tetrazol-5-yl, 1,2,3,4 -Tetrazol-1-yl, benzo [b] -furan-2-yl, naphtho [2,1-b] -furan-2-yl, benzo [b] -thiophon-2-yl, naphtho [2,1- b] -thiophene-2-yl, pyrimidin-2-yl, pyridin-2-yl, quinazolin-4-yl or chinazolin-2-yl, and - if n = 0 - also naphthyl, stilbene -4-yl, benzo [b] furan-6-yl, dibenzofuran-3-yl, di-benzofuran-2-yl, quinoxalin-5-yl, quinazolin-6-yl or 2H-benzotriazol-5-yl and n is 0, 1 or 2, where the substituents X, Y, Q and the other cyclic radicals can be further substituted by non-chromophoric substituents customary for white toners, are suitable for whitening a wide variety of synthetic, semi-synthetic and natural organic high-molecular materials. |
| priorityDate | 1977-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 194.