http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S57145889-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ab3e1d2b9a4794709fe79651849d76e
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N57-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N57-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-38
filingDate 1981-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_799c811eccb2df68694b1ed285309ff9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_469e416d0c83dbd619c0a61f303d5f25
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8bef6153b3a193e349929acef5f5b928
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc1b293d02ef30af5cdca123a03470a7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8daa73289524d05e416b6ff5fbefb965
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0d38402af6b9dc4c960d53369d552c3
publicationDate 1982-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S57145889-A
titleOfInvention Organic phosphoric acid anhydride derivative
abstract NEW MATERIAL:An organic acid anhydride derivative shown by the formulaI (R 1 and R 5 are lower alkyl; R 2 and R 3 are H, lower alkyl; R 4 is lower alkoxy, lower alkyl, phenyl). n USE: An insecticide, acaricide, nematocide. Having activity on Nephotettix cincticeps Uhlera having resistance to various kinds of organic phosphorus type insecticides and carbamate type insecticides. Having low toxicity to mammals and no phytotoxicity to useful plants. n PROCESS: An amidothiophosphoryl halide shown by the formula II (Hal is halogen) is reacted with an alkali salt or ammonium salt of phophoro or phosphonothioate shown by the formula III to give a compound shown by the formulaI. The reaction is preferably carried out in the presence of an acid binder (e.g., TEA) in case of necessity in an inert organic solvent at 0W120°C. n COPYRIGHT: (C)1982,JPO&Japio
priorityDate 1981-03-05-04:00^^<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/substance/SID419559532
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524042
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19690831
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559374
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID276
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414022206
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24404
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID94400
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14812
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID94400

Total number of triples: 32.