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filingDate 2000-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d3b8ed6179cea73687911ea9d8057d2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8a235b71e24cb8ab1851cea0e3f3a0f7
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed09f4e2671e5ff6672e438a9c759353
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_408abb34cc1beba8912f4d87f24fed6d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4fb915920612fd8326c0babb96368b97
publicationDate 2003-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0204412-A2
titleOfInvention Insecticidal aromatic diamide derivatives and compositions containing them and their use
abstract In the compounds of the present invention, in the formula (I), A1 is each an optionally substituted saturated or unsaturated alkylene chain, B is -O- or -N (R4) - wherein R4 is hydrogen, alkyl, haloalkyl, alkenyl, haloalkenyl, cycloalkyl , alkylcarbonyl, haloalkylcarbonyl, optionally substituted phenylcarbonyl, phenylalkoxycarbonyl, or phenylalkyl, R1 is hydrogen, alkyl, haloalkyl, alkoxyalkyl, alkylthioalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkyl, halo-cycloalkyl, optionally substituted phenyl, phenylalkyl, optionally substituted heterocyclic group, -P (= W1) (- OR5) (- OR6), -C (= W1) -, -N (R5) (R6), -C (-) W1) -R5, -C (= W1) -W1-R7, -SO2-R7, -SO2-N (R5) (R6), -N (R5) (R6) or -N = C (R5) (R6) or B = -N (R 4) - where R 1 is -OR 5, - C (W 2) -N- (R 5) R 6 or C (W 2) -W 1 -R 7, R 2 and R 3 are hydrogen, c icloalkyl or -A2-R8, wherein A2 is -C (= O) -, -C (= S) - or -C (= NR9) -, or optionally unsaturated alkylene substituted by halogen, R8 is hydrogen, halogen , a cyclic, aromatic or heterocyclic hydrocarbon radical, cyano, nitro, or optionally substituted and optionally linked via -O-, -S-, -SO-, -SO2- or -N (R11) -, is defined as Q1-Q5 carbon or nitrogen, X and Y are halogen, cyano, nitro, cycloalkyl, halo-cycloalkyl, alkoxycarbonyl, optionally substituted phenyl, or heterocyclic, or -A5-R14, wherein A5 is -O-, -S- , -SO-, -SO2-, -C (= O) - or - C (= NOR13) -, optionally substituted halogen, unsaturated or unsaturated alkylene, R14 is hydrogen, halogen or individually substituted alicyclic, cyclic, aromatic s or heterocyclic hydrocarbon group, or X is an aromatic ring-linked fused ring n is 0-4, m is 1-5, Z1 and Z2 are independently O or S. HE
priorityDate 1999-12-22-04:00^^<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/CID4936
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID81723
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID66461
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7219
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID86005
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID93357
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419509881
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5353395
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426285928
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID91644
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153974
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412478856
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457814463
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID91650
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416224369
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415781416
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419509877
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412505152
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419516793
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID42586
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID93460

Total number of triples: 611.