http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-1775401-C

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9241aa5fc0d73f20d197bedd5a62a0c8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-125
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-46
filingDate 1990-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a4b859b28137df6f25f0ff0bc8ac8827
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ae623f540c998284479270460a2a693
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d8abebf22002e483431f57b02e4a8a97
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff67690fb7f953eb54c28a0872f99ebd
publicationDate 1992-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-1775401-C
titleOfInvention 2,5-bis-(4-aminophenylthio)-1,3,4-thiadiasol or 2,5-bis)4-aminophenyl-sulfonyl)-1,3,4-thiadiasol as light stabilizers of cellulose acetate
abstract The invention relates to heterocyclic compounds, in particular to 2,5bis (4-aminophenylthio) -1,3,4-thiadiazole or 2,5-bis (4-aminophenylsulfonyl) -1,3,4-thiaziazole use of cellulose acetate as light stabilizers. The goal is the creation of new, more active compounds. The preparation is carried out by condensation of equimolar amounts of 2,5-dimercapto-1,3,4-thiadiazole with 4-halide-nitrobenzene in an amide solvent medium, followed by reduction of the resulting dinitro compound. Yield,%: mp, ° C; gross-f-la: a) 85; [deg.] 25-227; Ci4HtzN4S3. b) 85; 191-193; COMMUNICATIONS New substances are more effective than the known 2, 6-dihydroxyphenylthio - 1,3,4-thiadiazole. 1 tab.
priorityDate 1990-04-10-04:00^^<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: 31.