http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-047964-A1
Outgoing Links
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|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e |
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| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C251-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N35-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C327-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-18 |
| filingDate | 2005-02-18^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82d161f0c55a53e578e716cf9dcd1430 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65df22129f8b5ce8c90cdf731bbc9063 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71ff415c98607bcc9c780d1a22d4de48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b43fda550dd5d050749bd417f9bebef1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9185c46956c6e34fad622a9f0814f5b0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d2b3f9ac592c575a7e7d663c806ea7f2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4710abfa3a19b469a0bee0224f29d994 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9d1fbdd3ce6195550522c4b14526ba6 |
| publicationDate | 2006-03-15^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-047964-A1 |
| titleOfInvention | DERIVATIVES OF DIFLUOROALQUENO INSECTICIDES AND NEMATICIDES, PESTICIDED COMPOSITIONS THAT CONTAIN THEM AND METHODS FOR PEST CONTROL THAT INVOLVE THEM. |
| abstract | This refers to insecticide and nematicide difluoroalkene derivatives. Methods for controlling a pest of invertebrates are also described which comprise contacting the pest of invertebrates or their environment with a biologically effective amount of a compound of the formula (1), an N-oxide itself or a suitable salt compound ( for example, as a composition described herein: Composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of the formula (1), an N-oxide thereof or a suitable salt of the compound and at least an additional component selected from the group consisting of a surfactant, a solid diluent, a liquid diluent and optionally a biologically active compound or additional agent: Spray composition containing the compound of formula (1) and a propellant; and a composition of bait containing said compound, one or more feed materials and optionally an attractor and a humectant Claim 1: A compound of the formula (1), an N-oxide thereof or an agronomic or non-agronomically suitable salt thereof, wherein Q is Q-1 or Q-2; Y is H, F, Cl, or CH3; A is CN, C1-6 alkyl, OR1a, SR1a, NR1aR2a or CONR1bR2b; Z is O, S or NR3; W is N or CR4; J1 and J2 are C1-6 alkyl, C2-6 alkenyl, C3-6 alkynyl, C3-7 cycloalkyl, C4-8 cycloalkylalkyl, C1-4 alkoxy, C2-6 alkoxycarbonyl or C2- alkylcarbonyl 6 or C2-6 alkylcarbonyl, each optionally substituted with a G and each optionally substituted with one or more R5, or J1 and J2 are G, NO2, CN, OH, NR6R7, CONR6R7, OCONR6R7, C1-4 alkyl sulfonyl, C (O) G or S (O) 2G; each G is independently a phenyl ring, a naphthyl ring system, a 5- or 6-membered heteroaromatic ring or a fused 8-, 9-, or 10-membered heterocyclic ring system, each ring or ring system optionally substituted with 1 at 5 R8; R1a and R1b are H, G, CN, or C1-6 alkyl, C2-6 alkenyl, C3-6 alkynyl; C3-7 cycloalkyl or C4-8 cycloalkylalkyl, each optionally substituted with one or more substituents selected from the group consisting of G, halogen, CN, NO2, C1-4 alkoxy, C1-4 alkylthio, C1 alkylsulfinyl -4, C1-4 alkylsulfonyl, C2-4 alkoxycarbonyl, C1-4 alkylamino, C2-8 dialkylamino and C3-6 cycloalkylamino; R2a and R2b are H, or C1-6 alkyl, C2-6 alkenyl, C3-6 alkynyl, C3-7 cycloalkyl or C4-8 cycloalkylalkyl, each optionally substituted with one or more substituents selected from the group which It consists of halogen, CN, NO2, C1-4 alkoxy, C1-4 alkylthio, C1-4 alkylsulfinyl, C1-4 alkylsulfonyl, C2-4 alkoxycarbonyl, C1-4 alkylamino, C2-8 dialkylamino and C3-6 cycloalkylamino, or R1a and R2a or R1b and R2b are taken together with the N to which they are attached to form a ring that includes 2 to 5 C atoms and optionally an additional N, S or O atom, the ring it is optionally substituted with 1 to 2 R5; R3 is H, C1-6 alkyl, C2-6 alkenyl, C3-6 alkynyl, C3-7 cycloalkyl or C4-8 cycloalkylalkyl R4 is H, C1-4 alkyl or CN; or R4 is a phenyl ring optionally substituted with 1 to 5 R8; each R5 is independently halogen, CN, NO2, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 1-6 haloalkyl, C 2-6 haloalkenyl, C 2- haloalkynyl 6, C3-6 halocycloalkyl, C1-4 alkoxy, C1-4 haloalkyl, C1-4 haloalkoxy, C1-4 alkylthio, C1-4 alkylsulfinyl, C1-4 alkylsulfonyl, C1-4 haloalkylsulfinyl, haloalkylsulfonyl C1-4, C1-4 alkylamino, C2-8 dialkylamino, C3-8 cycloalkylamino, C2-6 alkylcarbonyl, or C2-6 alkoxycarbonyl; R6 and R7 are each independently H, or C1-6 alkyl, C3-6 alkenyl, C3-6 alkynyl, C3-6 cycloalkyl, C2-6 alkylcarbonyl or C2-6 alkoxycarbonyl, each optionally substituted with halogen, or R6 and R7 can be taken together with the N to which they are attached to form a ring that includes 2 to 5 C atoms and optionally an additional atom of N, S or O, the ring is optionally substituted with halogen; each R8 is independently halogen, CN, NO2, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, C1-6 haloalkyl, C2-6 haloalkenyl, C2- haloalkynyl 6, C3-6 halocycloalkyl, C1-4 alkoxy, C1-4 haloalkoxy, C1-4 alkylthio, C1-4 alkylsulfinyl, C1-4 alkylsulfonyl, C1-4 haloalkyl, C1-4 haloalkyl, C1-4 haloalkylsulfonyl, C1-4 alkylamino, C2-8 dialkylamino, C3-6 cycloalkylamino, C2-6 alkylcarbonyl or C2-6 alkoxycarbonyl, or each R8 is independently a phenoxy ring or a phenyl ring, each ring optionally substituted with 1 to 5 R5; R 10 is H, or C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-7 cycloalkyl or C 4-8 cycloalkylalkyl, each optionally substituted with one or more substituents selected from the group consisting of halogen, CN, NO2, C1-4 alkoxy, C1-4 alkylthio, C1-4 alkylsulfinyl, C1-4 alkylsulfonyl, C2-4 alkoxycarbonyl, C1-4 alkylamino, C2-8 dialkylamino and cycloalkylamino C3-6; or R10 is C1-6 alkylthio, CN, CO2R12, CONR12R13 or phenyl optionally substituted with 1 to 5 R11; each R11 is independently halogen, CN, NO2, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, C1-6 haloalkyl, C2-6 haloalkenyl, C2- haloalkynyl 6, halocycloalkyl e C3-6, alkoxy of C1-4, haloalkoxy of C1-4, alkylthio of C1-4, alkylsulfinyl of C1-4, alkylsulfonyl of C1-4, haloalkylthio of C1-4, haloalkylsulfinyl of C1-4, C 1-4 haloalkylsulfonyl, C 1-4 alkylamino, C 2-8 dialkylamino, C 3-6 cycloalkylamino, C 2-6 alkylcarbonyl, or C 2-6 alkoxycarbonyl; R12 and R13 are each independently H or C1-6 alkyl; and n is 1, 3 or 5; as long as (1) when Y is F, Z is S, n is 1, A is SR1a, NR1aR2a and W is N, then J1 is not alkyl, G, CN or cycloalkyl; (2) J1 is not 3- (4- trifluoromethyl) pyridinylcarbonyl or an N-oxide thereof; (3) when R10 is H, methyl, ethyl, phenyl or 4-fluorophenyl and J2 is phenyl substituted with R8, then R8 is not 2-fluoroethoxy; (4) when Z is NH, W is N and AQ is SR1a, then J1 is not phenyl substituted at positions 2 and 6 with alkyl or cycloalkyl; and (5) when Z is NR3, W is N or CH, A is NR1aR2a and R1a or R2a is H or alkyl, then J1 is not CN or NO2. |
| priorityDate | 2004-02-18^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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