http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S56131553-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-05 |
filingDate | 1980-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_38db98fcdc7d2de0c350e4f1a992829c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a6dbb6e98f8181e57b0e02192aec050 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8721f21b3ed446909e0b26e24ac4628 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26612ed39cb6628b01bf7b02bebcf9ea http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0890d199d57dd2f34eaa166d0eb4e55e |
publicationDate | 1981-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-S56131553-A |
titleOfInvention | Optically active n-benzyl-haloacetamide derivative, its preparation, and herbicide containing said derivative as effective component |
abstract | NEW MATERIAL:The titled derivative of formula I (X is halogen; R is H ormethyl; the mark * denotes asymmetric carbon). n EXAMPLE: d-N-(α,α-Dimethylbenzyl)-α-bromo-t-butylacetamide. n USE: Herbicide effective against weeds in a plowed field, annual weeds in a paddy rice field, and perennial weeds such as flatstage. It is harmless to important crops such as rice plant, soybean, cotton, etc., and vegetables such as lettuce. n PROCESS: For example, an α-halo-t-butylacetic acid is optically resolved with optically active α-methylbenzylamine or optically active 1-phenyl-2-(p-tolyl)-ethylamine. The resulting optically active α-halo-t-butylacetic acid of formula II or its reactive derivative is made to react with α,α-dimethylbenzylamine or α,α,p-trimethylbenzylamin to obtain the objective compound. n COPYRIGHT: (C)1981,JPO&Japio |
priorityDate | 1980-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 42.