http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2381499-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 |
| filingDate | 2006-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2012-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a7b10709d294a8cc221ff064a0e9c082 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69aa7b2a8081f8c62ef468ae79e3fc9f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40b9c90b909f44afeb622a09416fb68e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_354f00d4851a54fb7b51e64626ee7ea6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e263396420ae8f73820bb29df6933f71 |
| publicationDate | 2012-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2381499-T3 |
| titleOfInvention | 5-Aryloxisazolines to control invertebrate pests |
| abstract | A compound of Formula 1, an N-oxide or a salt thereof, wherein: A1, A2 and A3 are independently selected from the group consisting of CR3 and N; B1, B2 and B3 are independently selected from the group consisting of CR2 and N; R1 is C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C4-C7 alkylcycloalkyl or C4-C7 cycloalkylalkyl, each optionally substituted with one or more substituents independently selected from R6; each R2 is independently H, halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkyl thio, C1-C6 haloalkyl thio, C1-C6 alkyl sulfinyl, C1-C6 haloalkyl sulfinyl, C1-C6 alkyl sulfonyl, halo C1-C6 alkyl sulfonyl, C1-C6 alkyl amino, C2-C6 dialkyl amino, C2-C4 alkoxycarbonyl, -CN or -NO2; each R3 is independently H, halogen, C1-C6 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C3-C6 haloalkenyl, C2-C6 alkynyl, C3-C6 haloalkynyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1 alkoxy -C6, haloalkoxy C1-C6, alkyl C1-C6 thio, haloalkyl C1-C6 thio, C1-C6 alkyl sulfinyl, haloalkyl C1-C6 sulfinyl, alkyl C1-C6 sulfonyl, haloalkyl C1-C6 sulfonyl, -N (R4) R5 , -C (W) N (R4) R5, -C (W) OR5, -CN or -NO2; Q is a 5 or 6 membered phenyl ring or a saturated or unsaturated heterocyclic ring, each ring optionally substituted with one or more substituents independently selected from halogen, C1-C6 alkyl, C1-C6 haloalkyl, C3-C6 cycloalkyl, halocycloalkyl C3-C6, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkyl thio, C1-C6 alkylthio thio, C1-C6 alkyl sulfinyl, C1-C6 haloalkyl sulfinyl, C1-C6 alkyl sulfonyl, C1-C6 haloalkyl sulfonyl ester, -CN, -NO2, -N (R4) R5, -C (W) N (R4) R5, -C (O) OR5 and R8; each R4 is independently H, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C4-C7 alkylcycloalkyl, C4-C7 cycloalkylalkyl, C2-C7 alkylcarbonyl or C2-C7 alkoxycarbonyl; each R5 is independently H; or C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C4-C7 alkylcycloalkyl or C4-C7 cycloalkylalkyl, each optionally substituted with one or more substituents independently selected from R7; each R6 is independently halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkyl thio, C1-C6 alkyl sulfinyl, C1-C6 alkyl sulfonyl, -CN or -NO2; each R7 is independently halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkyl thio, C1-C6 alkyl sulfinyl, C1-C6 alkyl sulfonyl, -CN, -NO2 or Q1; each R8 is independently a phenyl ring or a pyridinyl ring, each ring optionally substituted with one or more substituents independently selected from R9; each R9 is independently halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkyl, C1-C6 alkyl thio, C1-C6 haloalkyl thio, C1-C6 alkyl sulfinyl, C1-C6 haloalkyl sulfinyl, C1-C6 alkyl sulfonyl, halo C1-C6 alkyl sulfonyl, C1-C6 alkyl amino, C2-C6 dialkyl amino, C2-C4 alkylcarbonyl, C2-C4 alkoxycarbonyl, C2-C7 alkylcarbonyl, C3-C7 aminocarbonyl alkyl, -OH , -NH2, -COOH, -CN or -NO2; each Q1 is independently a phenyl ring or a 5 or 6 membered saturated or unsaturated heterocyclic ring, each ring optionally substituted with one or more substituents independently selected from halogen, C1-C6 alkyl, C1-C6 haloalkyl, C3-C6 cycloalkyl , C3-C6 halocycloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 thio alkyl, C1-C6 haloalkyl thio, C1-C6 alkyl sulfinyl, haloalkyl C1-C6 sulfinyl, C1-C6 alkyl sulfonyl, haloC1-C6 alkyl sulfonyl, C1-C6 alkyl amino, C2-C6 dialkyl amino, -CN, -NO2, -C (W) N (R10) R11, -C (O) OR11 and R12; each R10 is independently H, C1-C6 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C4-C7 alkylcycloalkyl, C4-C7 cycloalkylalkyl, C2-C7 alkyl or C2- alkoxy C7 carbonyl; each R1 is independently H; or C1-C6 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C4-C7 alkylcycloalkyl, C4-C7 or R12 cycloalkylalkyl; each R12 is independently a phenyl ring or a pyridinyl ring, each ring optionally substituted with one or more substituents independently selected from R13; Each R13 is independently halogen, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 thio alkyl, C1-C6 thio haloalkyl, C1-C6 alkyl sulfinyl, C1-C6 alkyl sulfinyl, C1-C6 alkyl sulfonyl, halo C1-C6 alkyl sulfonyl, C1-C6 alkyl amino, C2-C6 dialkyl amino, C2-C4 alkylcarbonyl, C2-C4 alkoxycarbonyl, C2-C7 alkylcarbonyl, C3-C7 aminocarbonyl alkyl, -OH , -NH2, -COOH, -CN or -NO2; each W is independently O or S; n is 1 or 2. |
| priorityDate | 2005-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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