http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100438751-B1

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filingDate 1997-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2005-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100438751-B1
titleOfInvention Insecticide compositions, methods of controlling pests using the same and plant propagation materials treated by the method
abstract The present invention provides compounds of formula (A) in free or salt form, optionally one or more tautomers in free or salt form, and the following compounds, azamethicose; Chlorfenbin phos; Cypermethrin, cypermerin high-cis; Cyclo margin; Diafenthiuron; Diazinon; Dichlorbos; Dicrotophos; Dicyclanyl; Phenoxycarb; Fluazuron; Furathiocarb; Isazo force; Jodhfenfoss; Quinoprene; Lufenuron; Methacryfoss; Methidathione; Monochromatic force; Phosphamidone; Propenoforce; Diphenols; Materials obtainable from Bacillus thuringiensis strain GC91 or NCTC11821; Pymetrozine; Bromopropylate; Methoprene; Disulfutone; Quinal force; τ-fluvalinate; Compositions for controlling pests and pests of Acarita, pest control methods, methods for preparing the compositions, uses thereof and their use, including various amounts of combinations with one or more of thiocyclam or thiomethone and one or more adjuvants Treated plant propagation material, and the use of a compound of formula A for the preparation of a composition.n n n Formula An n n n n n n n In Formula A above,n n n A is unsubstituted or, depending on the likelihood of substitution in the ring system, mono- to tetrasubstituted radial or non-aromatic monocyclic or bicyclic heterocycle radicals, wherein substituent A is C 1-3 alkyl, C 1-3 Alkoxy, halogen, halo-C 1-3 alkyl, cyclopropyl, halocyclopropyl, C 2-3 alkenyl, C 2-3 alkynyl, halo-C 2-3 alkenyl, halo-C 2-3 alkynyl , Halo-C 1-3 alkoxy, C 1-3 alkylthio, halo-C 1-3 alkylthio, allyloxy, propazyloxy, allylthio, propazylthio, haloallyloxy, haloallylthio, cyano and Selected from the group consisting of nitro,n n n R is hydrogen, C 1-6 alkyl, phenyl-C 1-4 alkyl, C 3-6 cycloalkyl, C 2-6 alkenyl or C 2-6 alkynyl,n n n X is N-NO 2 or N-CN.
priorityDate 1996-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID402
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID236788
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4111
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412419288
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID463830
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID307658
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454973655
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID340537
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID132711
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID536013
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID13429
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86738752
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID1452691
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID1204166
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID877804
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4006
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID3435
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411985344

Total number of triples: 302.