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filingDate 1996-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13e35c6915bb03af9a6132bb9d5049c0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24dd2a0a989eec19cb49f88de72480ac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef2fbcc57d263397fbea133e7bb60aba
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publicationDate 2004-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2202488-T3
titleOfInvention PESTICIDE COMPOUNDS, COMPOSITIONS THAT CONTAIN THEM AND THEIR PREPARATION PROCEDURE.
abstract THE INVENTION REFERS TO COMPOUNDS OF THE GENERAL FORMULA (I), ITS OPTIMALLY ACTIVE ISOMERS AND THEIR SALTS, IN WHICH AR = AN ALICICLIC, AROMATIC OR HETEROATOMOS HETEROATOMOS CONTAINING A HETEROCICLICAL UNIT, OPTIONALLY A SUBSTITUTE ONE ALCOXI, METHYLENDIOXI, RENT, HALOGEN, HALOALKYL OR NITRO AND / OR CONDENSED GROUPS WITH A BENZENE RING; R 1, R 2 = INDEPENDENTLY, H, RENT, ALQUENILO, HALOALQUILO, PHENYL, SUBSTITUTED PHENYL, CYCLALQUILO, R 3, R 4 = INDEPENDENTLY, H, RENT, ALQUEN ILO, HALOALQUILO, PHENYLLO, RENOUS, CENYL R 4 FORM TOGETHER = O, Y = C; PO OR YR 3 R SUP, 4 TOGETHER WITH A GROUP (A); X = - O -; - NR 10 -, R 9 = H, RENT, PHENYL, REPLACED PHENYL; R 10 = H, RENT; R5, R6, R7, R8 ARE, INDEPENDENTLY, H, RENT, ALKYLENE, HALOALKYL, OR AR - (CR 1 R 2) M (YR 3 R 4 N - X - OR FORM A CARBOXIMIDE GROUP TOGETHER; E = H, HALOGEN , METHYLE; M = 0, 1, 2; N = 0, 1; O = 0, 1, 2; P = 0, 1, 2 WITH THE CONDITION THAT THE SUM OF THE ATOMS AND GROUPS OF THE PONTEO STRUCTURE ( CR 2 R 2) M - (CR SUP, 3 R 4 N - X (CR 5 R 6) O - (CR 7 R 8) P SEA 3 AND THE STRUCTURE - CC - E FORM A LINEAR CHAIN WITH THE BRIDGE ATOMS , WHICH CONSISTS OF 6 ATOMS THAT PREFERREDLY ENDED IN A METHYL GROUP, AND WITH THE CONDITION ALSO THAT, IF AR REPRESENTS A NAFTILO GROUP, AND BE AN ATOM OF C, X BE AN ATOM OF O, YR 3 YR 4 DO NOT BE TOGETHER = O. THE COMPOUNDS OF THE GENERAL FORMULA (I) OF THE PRESENT INVENTION CAN BE USED AS ACTIVE INGREDIENTS OF PESTICIDES, PREFERREDLY AS ANTIROPOCIDED COMPOSITIONS, AND AS SYNERGISTIC PRODUCTS OF OTHER INGREDIENTS WITH AN ANTHROPOCIDE ACTIVITY.
priorityDate 1995-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12313811
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523814
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419514522
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419509881
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID632
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419573132
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3017
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86103
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393705
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4270
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419526849
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419574264
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID31645
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419572902
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID7539
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394873
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425914843
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408720137
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2566
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3283
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID632
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16683004
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID390977
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6537963
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID91741
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415711252

Total number of triples: 303.