http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2099050-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-14 |
| filingDate | 1993-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a42a2379e1fb8161b9eab5830d8385d9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1585e0bdac869ced13e2363f4245222a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7866be3bb82e66694b0a119d4ad90e4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d3f0dec673eaa436fa28ce8f5d110cb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_281d654b00c99fb8f95b84aa74a753b6 |
| publicationDate | 1994-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CA-2099050-A1 |
| titleOfInvention | N-acyldihydroquinoline derivatives, a method for producing the same and their use as herbicides |
| abstract | ABSTRACT OF THE DISCLOSURE Novel N-acyldihydroquinoline derivatives represented by the formula (I), (I) wherein each of R1, R2 and R3, which may be the same or different, represents a hydrogen atom; a halogen atom, a C1-C6 alkyl group; a C1-C6 alkoxy group; a halo-C1-C6 alkyl group; a halo-C1-C6 alkoxy group; a (C1-C6 alkoxy)carbonyl group; a C1-C6 alkylthio group; a C1-C6 alkylamino group; a di(C1-C6 alkyl)amino group; a phenyl group; or a phenoxy group, each of R4 and R5, which may be the same or different, represents a hydrogen atom or a C1-C6 alkyl group, or R4 and R5 are bonded together at their ends to form a C2-C5 alkylene group, R6 represents a hydrogen atom; a halogen atom; an amino group; a C1-C6 alkylamino group; a di(C1-C6 alkyl)amino group; a (C1-C6 alkoxy)carbonylamino group, a cyano group; or a group represented by the formula, -C(=O)-Y-R7 (wherein Y represents an oxygen atom or a sulfur atom and R7 represents a hydrogen atom; a C1-C10 alkyl group; a C2-C10 alkenyl group; a C2-C10 alkynyl group; a halo-C1-C10 alkyl group; a halo-C2-C10 alkenyl group; a halo-C2-C10 alkynyl group; a C3-C10 cycloalkyl group; a C3-C10 cycloalkenyl group; a C1-C10 alkoxy-C1-C10 alkyl group; a C1-C10 alkylamino-C1-C10 alkyl group; a di(C1-C10 alkyl)amino-C1-C10 alkyl group; a furyl-C1-C10 alkyl group; a thienyl-C1-C10 alkyl group; a C1-C10 alkylamino group; a di(C1-C10 alkyl)amino group; -N=CH(C1-C10 alkyl) group; group; or a phenyl group optionally substituted with at least one member selected from the group consisting of (C1-C6 alkoxy)carbonyl groups, halogen atoms and C1-C6 alkyl groups; or a phenyl-C1-C6 alkyl group optionally substituted with at least one member selected from the group consisting of (C1-C6 alkoxy)carbonyl groups, halogen atoms and C1-C6 alkyl groups); or a group represented by the formula, (wherein each of R8 and R9, which may be the same or different, represents a hydrogen atom; a C1-C6 alkyl group; a C2-C6 alkenyl group; a C2-C6 alkynyl group; a halo-C1-C6 alkyl group; a halo-C2-C6 alkenyl group; a halo-C2-C6 alkynyl group; a C3-C6 cycloalkyl group; a C3-C6 cycloalkenyl group; an amino group; a C1-C6 alkylamino group; a di(C1-C6 alkyl)amino group; or a phenyl group optionally substituted with at least one member selected from the group consisting of halogen atoms and C1-C6 alkyl groups; or a phenyl-C1-C6 alkyl group optionally substituted with at least one member selected from the group consisting of halogen atoms and C1-C6 alkyl groups), X represents CH or a nitrogen atom, a method for producing the same and their use as herbicides. The N-acyldihydroquinoline derivatives have an excellent herbicidal activity and excellent selectivity between crops and weeds and therefore, can be used as an active ingredient for herbicides. |
| priorityDate | 1992-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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