http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-038860-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_981a37900e6991fb373304ed2ba5a703
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-02
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C239-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N35-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C317-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N41-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N33-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C243-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N57-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N35-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C281-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6506
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D335-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N41-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N41-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C239-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-81
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-42
filingDate 2003-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2005-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-038860-A1
titleOfInvention SUBSTITUTED ARILCETONES
abstract It refers to substituted aryl ketones, their use as pesticidal agents, especially herbicides, as well as procedures and intermediate products to obtain them. Claim 1: Compound of the formula (1) wherein A1 means a single bond, means O, S, or is a grouping selected from the group of structures (2), wherein: R8 means H, alkyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, alkylthio , alkylsulfinyl, alkylsulfonyl, alkenyl, alquenilcarbonilalquilo, alqueniloxicarbonilalquilo, alkynyl, alquinilcarbonilalquilo, alquiniloxicarbonilalquilo, cycloalkyl, cicloalquilcarbonilalquilo, cycloalkyloxycarbonylalkyl, cycloalkylalkyl, cicloalquilalquilcarbonilalquilo, cicloalquilalcoxicarbonilalquilo, aryl, arylcarbonylalkyl, aryloxycarbonylalkyl, arylalkyl, arylalkoxycarbonylalkyl arylalkylcarbonylalkyl or substituted, respectively, if desired; A2 means alkanediyl (alkylene), alkenodiyl or alkynediyl; A3 means O, S, or is a group selected from the group of structures (3) or (4) where: R9 means H or means substituted, respectively, where appropriate alkyl, alkylcarbonyl, alkoxycarbonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkenyl, alkenylcarbonyl, alkenyloxycarbonyl, alkynyl, alkynylcarbonyl, alkynyloxycarbonyl, cycloalkyl, cycloalkylcarbonyl, cycloalkyloxycarbonyl, cycloalkylalkyl, cycloalkylalkylcarbonyl, cycloalkylalkoxycarbonyl, aryl, arylcarbonyl, aryloxycarbonyl, arylalkyl, arylalkylcarbonyl, arylalkoxycarbonyl, heterocyclyl, heterocyclylcarbonyl or heterocyclylalkyl, or R9 together with R2 and the N with which are linked means a substituted heterocycle if appropriate, R10 means H, formyl or substituted, respectively, where appropriate alkyl, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkenyl, alkenylcarbonyl, alkenyloxycarbonyl, alkynyl, alkynylcarbonyl or alkynyloxycarbonyl, cycloalkyl, cycloalkylcarbonyl, cycloalkyloxycarbonyl, cycloalkylamino carbonyl, cycloalkylalkyl, aryl, arylcarbonyl, aryloxycarbonyl, arylaminocarbonyl, arylalkyl, arylalkylcarbonyl, arylalkoxycarbonyl, heterocyclyl, heterocyclylcarbonyl or heterocyclylalkyl, R1 is H or alkyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, arylcarbonylalkyl, heterocyclyl, or heterocyclylalkyl, substituted, respectively, where appropriate; R2 is H, formyl, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkenyl, alkenylcarbonyl, alkenyloxycarbonyl, alkynyl, alkynylcarbonyl, alkynyloxycarbonyl, cycloalkyl, cycloalkylcarbonyl, cycloalkyloxycarbonyl, cycloalkylaminocarbonyl, cycloalkylalkyl, aryl, arylcarbonyl, aryloxycarbonyl, arylaminocarbonyl, arylalkyl, arylalkylcarbonyl, arylalkoxycarbonyl, heterocyclyl, heterocyclylcarbonyl or heterocyclylalkyl, substituted, respectively, where appropriate; X means H, nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, halogen, or means alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino or dialkylaminosulfonyl, substituted, respectively, where appropriate; Y means H, nitro, cyano, carboxy, carbamoyl, thiocarbamoyl, halogen, or means substituted, respectively, where appropriate alkyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino or dialkylaminosulfonyl, substituted, respectively, if appropriate; and Z means one of the groupings of the group of structures (5), where m means the numbers 0 to 6, R3 means H, halogen, alkyl, alkylthio or aryl, substituted, respectively, where appropriate or - means, in the case in which m means 2- if appropriate also together with a second radical R3, O, or alkanediyl (alkylene); R4 means hydroxy, formyloxy, halogen, or means alkoxy, cycloalkoxy, alkylthio, cycloalkylthio, alkylsulfinyl, alkylsulfonyl, alkylcarbonyloxy, alkoxycarbonyloxy, alkylaminocarbonyloxy, alkylsulfonyloxy, alkenyloxy, alkynyloxy, aryloxy, arylthio, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyloxy, arylsilyl arylalkylthio, arylalkylsulfinyl, arylalkyl sulfonyl or heterocyclyl, substituted, respectively, if it contains at least 1 N atom and that is bridged through N, R5 means H, cyano, carbamoyl, thiocarbamoyl, halogen, alkyl, alkoxy, alkylthio , alkylsulfinyl, alkylsulfonyl, alkoxycarbonyl or cycloalkyl, substituted, respectively, where appropriate; R6 means H, or means substituted, respectively, where appropriate alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl, substituted, respectively, if appropriate; and R7 means hydroxy, formyloxy, alkoxy, cycloalkoxy, alkylcarbonyloxy, alkoxycarbonyloxy, alkoxycarbonylalkoxy, alkylaminocarbonyloxy, alkylsulfonyloxy, alkenyloxy, alkynyloxy, arylalkoxy, arylcarbonyloxy, arylcarbonylalkoxy, arylsulfonyloxy, respectively, if appropriate, respectively.
priorityDate 2002-03-05-04:00^^<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/SID457444288
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392901

Total number of triples: 62.