http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1311761-C
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-153 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-052 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-048 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-044 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 |
filingDate | 1988-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1992-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65df22129f8b5ce8c90cdf731bbc9063 |
publicationDate | 1992-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CA-1311761-C |
titleOfInvention | Insecticidal substituted indazoles |
abstract | TITLE INSECTICIDAL SUBSTITUTED INDAZOLES Abstract of the Disclosure Aninsecticidal compound of the following formula is disclosed: A compound of the formula I wherein Q is A is a 1, 2 or 3-atom bridge having 0 to 3 carbon atoms and 0 to 1 oxygen atom, NR6 group, of S(O)q group, wherein each carbon individually can be substituted with 1 to 2 substituents selected from 1 to 2 halogen, Cl to C6 alkyl, C2 to C4 alkoxycarbonyl or phenyl optionally substituted with 1 to 3 substituents selected from W and one of the carbon atoms can be C(O) or C(S); B is H, Cl to C6 alkyl, Cl to C6 haloalkyl, C2 to C6 alkenyl, C2 to C6 haloalkenyl, C2 to C6 alkynyl, OR7, C2 to C6 alkoxyalkyl, C2 to C6 cyanoalkyl, C3 to C8 alkoxycarbonylalkyl, CO2R3, C(O)R3, C(O)NR3R4, C(S)NR3R4, C(S)R3, C(S)SR3, phenyl, phenyl substituted by (R5)p, benzyl, or benzyl substituted with 1 to 3 substituents independently selected from W; J is H, Cl to C4 alkyl or phenyl optionally substituted with W; K is H or CH3; W is halogen, CN, NO2, Cl to C2 alkyl, Cl to C2 haloalkyl, Cl to C2 alkoxy, Cl to C2 halo-alkoxy, Cl to C2 alkylthio, Cl to C2 halo-alkylthio, Cl to C2 alkylsulfonyl or Cl to C2 haloalkylsulfonyl: R1, R2 and R5 are independently R3, halogen, CN, N3, SCN, NO2, OR3, SR3, SOR3, SO2R3, OC(O)R3, OSO2R3, CO2R3, C(O)R3, C(O)NH3R4, SO2NR3R4, NR3R4, NR4C(O)R3, OC(O)NHR3, NR4C(O)NHR3, NR4SO2R3, or when m, n or p is 2, R1, R2 or R5 can be taken together to form a 5 or 6 membered fused ring as -OCH2O-. -OCH2CH2O-, or -CH2CH2O-, each of which can be substituted with 1 to 4 halogen atom6 or 1 to 2 methyl groups; R3 is H, Cl to C6 alkyl, Cl to C6 haloalkyl, C2 to C6 alkenyl, C2 to C6 haloalkenyl, C2 to C6 alkynyl, C2 to C6 haloalkynyl, C2 to C6 alkoxyalkyl, C2 to C6 alkylthioalkyl, Cl to C6 nitroalkyl, C2 to C6 cyanoalkyl, C3 to C8 alkoxycarbonylalkyl, C3 to C6 cycloalkyl, C3 to C6 halocycloalkyl, phenyl, benzyl, or phenyl or benzyl substituted with 1 to 3 substituents independently selected from W; R4 is H, Cl to C4 alkyl or R3 and R4 can be taken together as (CH2)4, (CH2)5 or (CH2CH2OCH2CH2); R6 is H, Cl to C4 alkyl, Cl to C4 haloalkyl, C2 to C4 alkenyl, C2 to C4 haloalkenyl, phenyl, benzyl, phenyl optionally substituted with W or benzyl optionally substituted with W; R7 is H, Cl to C4 alkyl, C2 to C4 alkenyl, C2 to C4 alkynyl, C2 to C4 alkylcarbonyl, C2 to C4 alkoxycarbonyl, Cl to C4 alkylsulfonyl; X is 0 or S: n is 1 to 4; m is 1 to 5; p is 1 to 3 q is 0 to 2; and Y is H, Cl to C6 alkyl, benzyl, C2 to C6 alkoxyalkyl, CHO, C2 to C6 alkylcarbonyl, C2 to C6 alkoxycarbonyl, C2 to C6 haloalkylcarbonyl, C1 to C6 alkylthio, Cl to C6 haloalkylthio, phenylthio, or phenylthio substituted with 1 to 3 substi-tuents independently selected from W. |
priorityDate | 1987-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 233.