http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0492367-B1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2becc3642f2fd1e03f63bf24e23a1111 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N41-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N55-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N25-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-653 |
| filingDate | 1991-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2000-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f5e54368461e7ed98e078f700f30239 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_23b348147e8a02d2587e224a49bea36a |
| publicationDate | 2000-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0492367-B1 |
| titleOfInvention | Mixtures of herbicides and antidotes |
| abstract | Co-administration of phenyl or naphthyl safener with sulfonyl-urea or imidazolinone herbicide to reduce phytotoxic side effects of herbicide. Herbicide composition comprises: (a) one or more sulfonyl-urea or imidazolinone herbicides; and (b) one or more phenyl or naphthyl derivatives of formula (I) or (II); excluding combinations of imidazolinones with (II). X = H, halo, 1-4C alkyl, 1-4C alkoxy, NO2 or 1-4C haloalkyl; Y = halo, 1-4C alkyl, 1-4C alkoxy, NO2 or 1-4C haloalkyl; R' = 1-2C alkylene (optionally substituted by 1-2 1-4C alkyl); Z' = OR1, SR1 or NR1R; R = H, 1-6C alkyl, 1-6C alkoxy or optionally substituted phenyl; R1 = H; 1-18C alkyl, 3-12C cycloalkyl, 2-8C alkenyl or 2-8C alkynyl (each optionally substituted by one or more halo, OH, 1-8C alkoxy, 1-8C alkylthio, 2-8C alkenylthio, 2-8C alkynylthio, 2-8C alkenyloxy, 2-8C alkynyloxy, 3-7C cycloalkyl, 3-7C cycloalkoxy, CN, mono- or di-1-4C alkylamino, 1-8C alkoxycarbonyl, 2-8C alkenyloxycarbonyl, 1-8C alkylthiocarbonyl, 2-8C alkynycarbonyl, 1-8C alkylcarbonyl, 2-8C alkenylcarbonyl, 2-8C alkynylcarbonyl, 1-(hydroxyimino)-1-6C alkyl, 1-(1-4C alkylimino)-1-6C alkyl, 1-(1-4C alkoxyimino)-1-6C alkyl, 1-8C alkylcarbonylamino, 2-8C alkenylcarbonylamino, 2-8C alkynylcarbonylamino, aminocarbonyl, mono- or di-1-8C alkylaminocarbonyl, 2-8C alkenylaminocarbonyl, 2-8C alkynylaminocarbonyl, 1-8C alkoxycarbonylamino, 1-8C alkylaminocarbonylamino, 1-6C alkylcarbonyloxy (optionally substituted by halo, NO2, 1-4C alkoxy or optionally substituted phenyl); 2-6C alkenylcarbonyloxy, 2-6C alkynylcarbonyloxy or 1-8C alkylsulfonyl; phenyl, phenyl-1-6C alkoxy, phenyl-1-6C alkoxycarbonyl, phenoxy, phenoxy-1-6C alkoxy, phenoxy-1-6C alkoxycarbonyl, phenylcarbonyloxy, phenylcarbonylamino, or phenyl-1-6C alkylcarbonylamino (each optionally ring substituted by one or more halo, 1-4C alkyl, 1-4C alkoxy, 1-4C haloalkyl, 1-4C haloalkoxy or NO2); Si(R')3, OSi(R')3, (R')3Si-1-6C alkoxy, (R')2NOOC, O-N=C(R')2, N=C(R')2, O-N(R')2, CH(OR')2, O(CH2)mCH(OR')2 or R''O-CHR'''(OR'')-1-6C alkoxy); R' = H, 1-4C alkyl or phenyl (optionally substituted by one or more halo, 1-4C alkyl, 1-4C alkoxy, 1-4C haloalkyl or NO2); or R' + R' = 2-6C alkylene; m = 0-6; R'' = 1-4C alkyl; or R''+R'' = 1-6C alkylene; R''' = H or 1-4C alkyl; n = 1-5; W = a divalent heterocycle of formula (i)-(iii); R2 = H, 1-8C alkyl, 1-8C haloalkyl, 3-12C cycloalkyl or optionally substituted phenyl; R3 = H, 1-8C alkyl, 1-8C haloalkyl, 1-4C alkoxy-1-4C alkyl, 1-6C hydroxyalkyl, 3-12C cycloalkyl or tri-1-4C alkyl-silyl. An Independent claim is included for protection of plants from the phytotoxic side-effects of herbicides (a) by applying (I) or (II) at the same time or after, provided that a combination of imidazolinone herbicide and (II) is not applied. |
| priorityDate | 1990-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 239.