http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1208925-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-74 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N25-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C335-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-34 |
filingDate | 1983-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1986-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62a3fe78db150fc13d86dbf104e891f9 |
publicationDate | 1986-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CA-1208925-A |
titleOfInvention | N-sulfonyl-imino-thiocarbonic acid diesters as herbicide antagonists for the protection of rice crops |
abstract | N-Sulfonyl-imino-thiocarbonic acid diesters as herbicide antagonists for the protection of rice crops Abstract N-Sulfonyl-imino-thiocarbonic acid diesters of the formula I (I) wherein n is zero, 1, 2 or 3, R is halogen, cyano, nitro, a radical -Y-C1-C4-alkyl, -Y-C3-C6-alkenyl, -Y-C3-C6-alkynyl, -Y-phenyl or -Y-aralkyl, each unsubstituted or substituted by halogen, cyano, nitro, C1-C4-alkoxy, C1-C4-alkoxy-carbonyl, carbamoyl, sulfamoyl, C1-C4-mono- or dialkylcarbamoyl, C1-C4-mono- or dialkylsulfamoyl, or is a radical -COOR3, -NR3R4, -CONR3R4, -NHCONR3R or -SO2NR3R4, or two adjacent R's together form a 3- or 4-membered, saturated or unsaturated hydrocarbon chain, the chain members of which can be replaced once by oxygen or sulfur and/or once to three times by nitrogen, R1 and R2 independently of one another are each a C1-C4-alkyl, C3-C6-alkenyl, C3-C6-alkynyl, phenyl or aralkyl group, which can be unsubstituted or sub-stituted by halogen, cyano, nitro, C1-C4-alkyl, C1-C4-haloalkyl or C1-C4-alkoxy, or one of R1 and R2 can also be hydrogen or can form a 5- or 6-membered, saturated or unsaturated heterocycle which is bound by way of a carbon atom, contains 1-3 hetero atoms and can also be annularly-linked to a benzene ring, and which can be substituted by halogen and/or methyl, R3 is a C1-C4-alkyl, C3-C6-alkenyl, C3-C6-alkynyl or C3-C6-cycloalkenyl group, each of which can be sub-stituted by halogen, cyano, nitro or C1-C4-alkyl, R4 is hydrogen, the same as R3, or a phenyl or aralkyl group which can be substituted by halogen, cyano, nitro, C1-C4-alkyl, C1-C4-haloalkyl or C1-C4-alkoxy, or R3 and R4 together with the nitrogen atom to which they are bound form a 5- or 6-membered, saturated or unsaturated heterocycle which can also contain oxygen, sulfur, nitrogen or a methylimino group as ring member, X is oxygen or sulfur, and Y is the direct bond or an oxygen, sulfur, sulfinyl, sulfonyl, imino- or methylimino bridge are suitable as herbicide antagonists for protecting rice crops from phytotoxic damage which can occur as a result of herbicides. The N-sulfonyl-imino-thiocarbonic acid diesters are in part known. |
priorityDate | 1982-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 233.