http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4117247-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_33dafb5bbc2ec47ebcb7becbbe60f704
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C33-423
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-42
filingDate 1977-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1978-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10adc536cef3c806033baf63cdc1bed1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c0de1a013ab52e8cbdf1c0d5ad9b0b0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9f71663d0aadf8370824ae808b82aac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_92c3f6f9a2388f2b63a0cfe41686ba47
publicationDate 1978-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4117247-A
titleOfInvention Preparation of 1,1,1-trihalogeno-4-methyl-3-penten-2-ol
abstract A 1,1,1-trihalogeno-4-methyl-3-penten-2-ol is prepared by thermally isomerizing 1,1,1-trihalogeno-4-methyl-4-penten-2-ol. The isomerization reaction may be catalyzed by an acid or a transition metal of Group 6B, 7B or 8 of the Periodic Table of Elements, or a compound thereof. The 1,1,1-trihalogeno-4-methyl-3-penten-2-ol thus prepared is useful as a synergist for herbicides or a physiologically active compound, and, additionally, is useful as a starting material for the synthesis of 2,2-dimethyl-3-(2',2'-dihalogenovinyl)-cyclopropane carboxylic esters which are active ingredients of insecticides.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2537578-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4933511-A
priorityDate 1974-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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