http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0464542-A2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58 |
| classificationCPCInventive | 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/A01N43-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N35-10 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N35-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-16 |
| filingDate | 1991-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d305692778d0cdabbda2bf33e40f023 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0db24d3aaa0435e342930be41dd8b312 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a591e9071fc250112279fbce8278881 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8089c477fb06778a4d579377b726b4cb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65ce08d5faffbc416a70843d190aea8c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff7121fa934ed0a70d2f42cdc2bf3819 |
| publicationDate | 1992-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0464542-A2 |
| titleOfInvention | Herbicidal agents from cyclohexenon derivatives and 1,8-naphthalene-dicarboxylic anhydride as antidote |
| abstract | R 1 C 1-4 -C 4 -Alkyl; R 2 C 1 -C 4 -Alkyl; ggf. subst. C 3 -C 4 -Alkenyl, ggf. subst. Thenyl; oder einen Restn mit A = ggf. substtuiertes C 4 -Alkylen oder C 4 -Alkenylen; X = N0 2 ; CN; Carboxyl; Halogen; C 1 -C 4 -Alkyl; C 1 -C 4 -Alkoxy; C 1-4 -C 4 -Alkylthio; C 1 -C 4 -Halogenalkyl; C 1 - C 4 -Halogenalkoxy; C 1 -C 4 -Alkoxycarbonyl; ggf. subst. Benzyloxycarbonyl und ggf. subst. Phenyl; n = 0-3 oder 1-5 für den Fall, daß X für Halogen steht; R 3 ggf. substituiertes C 1 -C 4 -Alkyl; ggf. substituiertes 5- oder 6-gliedriges gesättigtes oder einfach ungesättigtes Ringsystem, welches neben Kohlenstoffgliedern ein Sauerstoff-, ein Schwefelatom oder eine Sulfoxid- oder Sulfongruppe enthalten kann; ggf. substituiertes Phenyl, Pyridyl, Pyrrolyl, Furyl, Thienyl, Imidazolyl, Pyrazolyl, Isoxazolyl, Isothiazolyl, Oxazolyl, Thiazolyl, Oxadiazolyl, Thiadiazolyl; R 4 H, OH oder, wenn R 3 für eine C 1 -C 6 -Alkyl steht, C 1 -C 6 -Alkyl R 5 H, CN, Halogen, C 1 -C 4 -Alkoxycarbonyl oder C 1 -C 4 -Alkylketoxim und R 6 H oder das Äquivalent eines landwirtschaftlich brauchbaren Kations, wobei R 3 nicht für 2-(Ethylthio)propyl steht, wenn R 1 Propyl und R 2 Ethyl bedeutet, sowie Verfahren zu ihrer Anwendung. Herbicidal compositions containing 1,8-naphthalenedicarboxylic acid anhydride and at least one herbicidal active ingredient from the group of cyclohexenones I, in which the substituents have the following meaning: R 1 is C 1-4 -C 4 alkyl; R 2 C 1 -C 4 alkyl; if necessary subst. C 3 -C 4 alkenyl, optionally subst. Thenyl; or a rest With A = optionally substituted C 4 alkylene or C 4 alkenylene; X = N0 2 ; CN; Carboxyl; Halogen; C 1 -C 4 alkyl; C 1 -C 4 alkoxy; C 1-4 C 4 alkylthio; C 1 -C 4 haloalkyl; C 1 - C 4 haloalkoxy; C 1 -C 4 alkoxycarbonyl; if necessary subst. Benzyloxycarbonyl and optionally subst. Phenyl; n = 0-3 or 1-5 if X is halogen; R 3 optionally substituted C 1 -C 4 alkyl; optionally substituted 5- or 6-membered saturated or monounsaturated ring system which, in addition to carbon members, may contain an oxygen, a sulfur atom or a sulfoxide or sulfone group; optionally substituted phenyl, pyridyl, pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, oxazolyl, thiazolyl, oxadiazolyl, thiadiazolyl; R 4 is H, OH or, if R 3 is C 1 -C 6 alkyl, C 1 -C 6 alkyl R 5 H, CN, halogen, C 1 -C 4 alkoxycarbonyl or C 1 -C 4 alkyl ketoxime and R 6 H or the equivalent of an agriculturally useful cation, where R 3 is not 2- (ethylthio) propyl when R 1 is propyl and R 2 is ethyl, and methods of using them. |
| priorityDate | 1990-07-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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