http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S56131553-A

Outgoing Links

Predicate Object
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

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID297
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226598328
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397689
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393755
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559581
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420263539
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4530
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235000159
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235000158
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID227623677
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68509
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14230778
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID3847
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4236
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7408
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID584050
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419515599
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID191086
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4236
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13020379
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415870272
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4530
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID3847

Total number of triples: 42.