http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2005716-C1

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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P7-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N53-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P7-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-743
filingDate 1991-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1994-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d1c2280329d68f863d5837ad4c7f406
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_27d5ffad77dfcbacc0b1ea083c6c24b8
publicationDate 1994-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2005716-C1
titleOfInvention Pentafluorobenzyl 1r,3s-2,2-dimethyl-3-(2-chlorophenyl) cyclopropancarboxylate
abstract FIELD: insecticide agent for use in agriculture. SUBSTANCE: pentafluorobenzyl 1R, 3S-2,2-dimethyl-3-(2-chlorophenyl) cyclopropancarboxylate of formula 1a, b , wherein a) , b) [α] 22 59 4 is prepared as mixture of isomers 1a and 1b in their ratio of 1: 2 to 1: 4, m. p. 82-84 C, SOCl 2 . Reagent 1: acid of formula II SOCl 2 as mixture of Z, E-isomers in their ratio of (2-4): 1. Reagent 2: CH 2 Cl 2 . Reaction conditions: reaction is carried out at temperature about 20 C for 10 hrs followed by removal of excess of pentafluorobenzyl alcohol in . EFFECT: increased yield of the end product. 2 tbl
priorityDate 1991-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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