http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2829234-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_173bc2c63b34988699010ba05e5b1376 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-647 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-14 |
| filingDate | 2016-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6af952d2def8b0b164642a1bc16662c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d367ec4c16e24ee9332ef5d37acc02c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82b63f796e3fee4ec4c25342bc090c15 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1aa75e0251053fd609ec5f5560d33c77 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bedc9179f625cf1f4bf286cbd0a6a625 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1c6f979b0cd9223c64d1c643255937f5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1c9bfa2f700ffc3a38073ac9b178fdce http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b3ba36fc021a15245a633d453d9ca7e7 |
| publicationDate | 2021-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2829234-T3 |
| titleOfInvention | Pesticide-active pyrazole derivatives |
| abstract | A compound of formula (I) ** (See formula) ** where R1 is selected from H, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C7 cycloalkyl, (C3-C7 cycloalkyl) (alkyl C1-C3), (C1-C6 alkyl) carbonyl, (C1-C6 alkoxy) carbonyl, aryl ((C0-C3) alkyl) and heteroaryl ((C0-C3) alkyl), where each of C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C7 cycloalkyl, (C3-C7 cycloalkyl) (C1-C3 alkyl), (C1-C6 alkyl) carbonyl, (C1-C6 alkoxy) carbonyl, aryl ((C0- C3)) and heteroaryl ((C0-C3) alkyl) is unsubstituted or is substituted with 1 to 7 substituents independently selected from halogen, cyano, C1-C6 alkyl and (C1-C6 alkoxy) carbonyl; Q is selected from H, hydroxy, -C (= O) H, C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkenyl, C2-C6 alkynyl, C3-C7 cycloalkyl, C3-C7 heterocycloalkyl, (C3-cycloalkyl C7) (C1-C3 alkyl), (C1-C3 alkyl) (C3-C7 cycloalkyl), aryl ((C0-C3) alkyl), heteroaryl ((C0-C3) alkyl), N- (C1-C6 alkyl) amino, N- (C1-C6 alkyl) carbonylamino and N, Ndi (C1-C6 alkyl) amino, where each of C1-C6 alkyl, C1-C6 alkoxy, C2-C6 alkenyl, C2-C6 alkynyl, C3-cycloalkyl C7, C3-C7 heterocycloalkyl, (C3-C7 cycloalkyl) (C1-C3 alkyl), (C1-C3 alkyl) (C3-C7 cycloalkyl), aryl ((C0-C3) alkyl), heteroaryl ((C0-C3 alkyl) )), N- (C1-C6 alkyl) amino, N- (C1-C6 alkyl) carbonylamino and N, Ndi (C1-C6 alkyl) amino is unsubstituted or is substituted with 1 to 7 substituents independently selected from halogen, hydroxyl, nitro, amino, cyano, C1-C6 haloalkyl, C1-C6 alkoxy, (C1-C6 alkoxy) carbonyl, - C (= O) OH, (C1-C6 alkyl) carbamoyl, -C (= O) NH2, -C (= S) NH2, (C3-C6 cycloalkyl) carbamoyl and phenyl; W is O or S; T is selected from ** (See formula) ** where * indicates the linkage to the pyrazole group; R6a, R7a, and R8a are independently selected from H, halogen, cyano, nitro, amino, C1-C6 alkyl, C1-C6 alkoxy, C3-C7 cycloalkyl, (C1-C6 alkyl) carbonyl, (C1-C6 alkyl) sulfanyl, (C1-C6 alkyl) sulfinyl and (C1-C6 alkyl) sulfonyl, where each of C1-C6 alkyl, C1-C6 alkoxy, C3-C7 cycloalkyl, (C1-C6 alkyl) carbonyl, (C1-C6 alkyl) sulfanyl , (C1-C6 alkyl) sulfinyl and (C1-C6 alkyl) sulfonyl is unsubstituted or substituted with 1 to 7 halogens; R6b, R7b and R8b are independently selected from H and C1-C6 alkyl, where C1-C6 alkyl is unsubstituted or substituted with 1 to 7 halogens; Z1 is selected from C1-C6 alkoxy, (C1-C4 alkoxy) (C1-C4 alkoxy), C3-C7 heterocycloalkyl, C1-C6 alkyl, C3-C6 cycloalkyl, where each C1-C6 alkoxy, (C1-C4 alkoxy) (C1-C4 alkoxy), C3-C7 heterocycloalkyl, C1-C6 alkyl and C3-C6 cycloalkyl is unsubstituted or is substituted with 1 to 7 substituents independently selected from halogen, hydroxy, nitro, amino, cyano, C1-C6 alkoxy , (C1-C6 alkoxy) carbonyl, -C (= O) OH, (C1-C6 alkyl) carbamoyl, (C3-C6 cycloalkyl) carbamoyl and phenyl; Z2 is selected from H, halogen, cyano, nitro, amino, C1-C6 alkoxy, C3-C7 heterocycloalkyl, C3-C7 cycloalkyl, C1-C6 alkyl, (C1-C6 alkyl) carbonyl, (C1-C6 alkyl) sulfanyl, (C1-C6 alkyl) sulfinyl and (C1-C6 alkyl) sulfonyl, where each of C1-C6 alkoxy, C3-C7 heterocycloalkyl, C3-C7 cycloalkyl, C1-C6 alkyl, (C1-C6 alkyl) carbonyl, (alkyl C1-C6) sulfanyl, (C1-C6 alkyl) sulfinyl and (C1-C6 alkyl) sulfonyl is unsubstituted or is substituted with 1 to 7 substituents independently selected from halogen, hydroxy, nitro, amino, cyano, C1-C6 alkoxy , (C1-C6 alkoxy) carbonyl, -C (= O) OH, (C1-C6 alkyl) carbamoyl, (C3-C6 cycloalkyl) carbamoyl and phenyl; Z3 is selected from H, C1-C6 alkyl, C1-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, aryl, and heteroaryl, where each from C1-C6 alkyl C1-C6 cycloalkyl, C2-C6 alkenyl, C2 alkynyl -C6, aryl and heteroaryl is unsubstituted or substituted with 1 to 7 substituents independently selected from halogen, hydroxy, nitro, amino, cyano, C1-C6 alkoxy, (C1-C6 alkoxy) carbonyl, -C (= O) OH, (C1-C6 alkyl) carbamoyl, (C3-C6 cycloalkyl) carbamoyl and phenyl; or an agrochemically acceptable salt or N-oxide thereof. |
| priorityDate | 2015-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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