http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-19751943-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e7ee05e5af286e73261ac75cee30782d |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-18 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D411-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P13-00 |
filingDate | 1997-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46d54a53f590e69b289f5ec9308099b0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e90d5acda2034f0331a87898c8fe1fca http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_afa579b6f480dc09c2dc63170a3a8064 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffd908770dd35ca57782f16ace9fea72 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ace3f8df48b87ee1d32ba2037303ed6a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b92ce75ab1d708284b659e3cf8690694 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96528d78c3b3e94e394b4b124b210af4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce0e03da278c94a53afde9d545aa0669 |
publicationDate | 1999-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | DE-19751943-A1 |
titleOfInvention | 1-Methyl-5-alkylsulfonyl-, 1-methyl-5-alkylsulfinyl- and 1-methyl-5-alkylthio-substituted pyrazolylpyrazoles, process for their preparation and their use as herbicides |
abstract | 1-(1-Methyl-3-pyrazolyl)pyrazole derivatives of formula (I) are new. R1 = 1-3C alkyl, 3-8C cycloalkyl or 2-3C alkenyl (all optionally substituted by halo); R2 = halo or CN; R3 = CN, NO2 or CSNH2; R4 = halo, 1-6C alkyl, 1-6C haloalkyl, NR5R6, NR5COR7, XR8, A, CH(R9)A, CH(R10)-C(R9)A, C(R10)=C(R9)A, CH2XR8, C?=CA, -(CH2)m-c(R11)(XR12)(XR13) or a group of formula (i) or (ii); A = CN, COOR14, C(NH)OR14, COR14 or CONR14R15; R5 = H or optionally halogenated 1-6C alkyl, 3-8C cycloalkyl, 2-6C alkenyl or 2-6C alkynyl; R6 = optionally halogenated 1-6C alkyl, 3-8C cycloalkyl, 2-6C alkenyl or 2-6C alkynyl, di(1-4C alkoxy) 1-3C alkyl or a group of formula (iv): R7 = H or optionally halogenated 1-4C alkyl or 3-8C cycloalkyl; R8 = optionally halogenated 1-6C alkyl optionally interrupted by O and/or S; R9 = H, 1-3C alkyl, halo, NH2, 1-4C alkylamino or di(1-4C alkyl)amino; R10 = H, 1-3C alkyl, halogen, NH2, OH, 1-4C alkylamino or di(1-4C alkyl)amino; R11 = H, 1-3C alkyl or XR12; R12, R13 = optionally halogenated 1-6C alkyl optionally interrupted by O and/or S; R14, R15 = 1-6C alkyl, 3-8C cycloalkyl, 2-6C alkenyl or 2-6C alkynyl (all optionally substituted by 1-4C alkoxy, 2-5C alkoxycarbonyl, CN or halo and optionally interrupted by O and/or S); or NR14R15 = optionally methyl-substituted 3-, 5- or 6-membered ring optionally containing an O atom; R16-R21 = H, 1-4C alkyl or 1-4C haloalkyl; or two of R16-R21 = bond; X = O or S; m, n and p = 0-2; and q = 1 or 2. |
priorityDate | 1997-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 140.