http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2247117-C1

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-14
filingDate 2003-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e45ec36871864a31c409f8fb1cd02374
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2c30ae4e937818f7d39bdf2fd79f483
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5ba4d0ad4910473471de02c2fca8ebc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42a0ae8687126f4476b524bd8facbcfb
publicationDate 2005-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2247117-C1
titleOfInvention Yellow-luminescence colorless organic luminophor and a method for preparation thereof
abstract FIELD: organic synthesis. n SUBSTANCE: invention provides novel compound: 1-[2-(4,6-dichloro-[1,3,5]triazine-2-ylamino)phenyl]-benzo[d][1,3]oxazine-4-one, characterized by yellow luminescence. Preparation of this compound comprises preliminarily preparing 2-(2-aminophenyl)-benzo[d][1,3]oxazine-4-one by reaction of anthralic acid with thionyl chloride followed by reaction of thus prepared compound with cyanuric acid chloride. Compound is characterized by fluorescence maximum at 560 nm and spare solubility in most organic solvents. The latter enables use of the compound in polygraphic inks as fluorescent pigment. n EFFECT: enlarged assortment of luminophors. n 2 cl, 1 dwg
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2587082-C2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2012069859-A1
priorityDate 2003-06-17-04:00^^<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: 38.