http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2517169-C2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0ec83c1631af3dc0e0aa55046d4d8b75
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-54
filingDate 2012-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_abe00814fd8d5782e0be57db5daf5818
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_015d4dc656139175a828bf77cc74cf74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13b4f15552fb0a074e00b6019d990f6e
publicationDate 2014-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2517169-C2
titleOfInvention METHOD OF PRODUCING S-PENTYLCARBOTHIOL-1aH,2'H-[1,2]PYRAZOLINO[3',4':1,9](C60-Ih)-[5,6]FULLERENE
abstract FIELD: chemistry. n SUBSTANCE: invention relates to a method of producing sulphur-containing fullerene derivatives and specifically to a method of producing S-pentylcarbothio-1aH,2'H-[1,2]pyrazolino[3',4':1,9](C 60 -I h )-[5,6]fullerene of formula (1), which can be used as effective nano-component additives for industrial oil, as well as a novel material for optoelectronics. The method involves reacting C 60 -fullerene with pentyldiazothioate of formula N 2 CHC(O)SC 5 H 11 in o-dichlorobenzene in molar ratio C 60 :diazothioate=0.01:(0.02-0.05), preferably 0.01:0.03 at 40°C for 0.5-1.5 hours. n EFFECT: method enables selective production of S-pentylcarbothio-1aH,2'H-[1,2]pyrazolino[3',4':1,9](C 60 -I h )-[5,6]fullerene with output of 41-58% . n 1 tbl
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2785691-C1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2785546-C2
priorityDate 2012-04-19-04:00^^<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: 28.