http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2906928-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N53-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N53-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N53-10
filingDate 1979-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5a8d4b4cac8d76cabc861a0346f3ed5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7e6f764d84d9c7f0461a69446ca7be5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf3aee179fee0bcc5dfb4856dda59b6a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b59494221f28227f4b86b2cd9b462bd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c77ba1a15457d7282f0816872833f04f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67422810b4d41e8c9971850d8e31f734
publicationDate 1979-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2906928-A1
titleOfInvention CHRYSANTHEMIC ACID DERIVATIVES, PRODUCTION AND USE OF THEREOF
abstract Optically active or racemic chrysanthemate esters of formula (I) are new. (where R1 and R2 are H, halogen or lower alkyl, or one of R1 and R2 can be lower alkoxycarbenyle; R3 is H, lower alkyl or 1-alkenyl). (I) are used in preparing pyrethrins of formula (II): (II) are known insecticides. As well as being intermediates for preparing (II), cpds. (I) themselves have insecticidal activity, e.g. giving knock-down times (KD50) of 20-50 min. against Musca domestica and Blattella germanica. Specific (I) includes 1 beta-hydroxy-2 beta-(cis-2-butenyl)-3-methylene-4 beta-cyclopentyl circled positive -trans-chrysanthemate.
priorityDate 1978-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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