http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20050115925-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-38 |
| filingDate | 2004-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e37e2d548fdd2a9bda3b1d9335bd1fa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9117c50f845d78b55afe2fa63f923ef http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_554697ecf08d564d251fa7ff2221595a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d00f8134a2b38c1e57a9e3e219e1693 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fdc1a0a9dc069edba25336436d7be51 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf39dc81fcba8a68b2a3cebf4b2cc1dd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8efee4ebbb7b074575edce800cf57a2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b30702b7decccf541fb6305310036770 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c060f25a28e0087fa2f686268d8d852 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8fc3c37f6ba3bd4d0c6ce8df28fcd726 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cabf0a8ddbc14c7d875080feaff715b9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6edb93a2acf9ee6a9d817b681bee4807 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_66350d70211ea3d166bea904a48d2549 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1661bc10a16683418312bbd5b9752b96 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c96766be83d6d54e93227a5d6cbbee2 |
| publicationDate | 2005-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-20050115925-A |
| titleOfInvention | Trifluoromethyl-thiophene carboxylic acid anilides and use thereof as fungicides |
| abstract | The present invention relates to trifluoromethyl-thiophene carboxylic acid anilide of formulas (I), (II) and (III).n n n <Formula I>n n n n n n n n <Formula II>n n n n n n n n <Formula III>n n n n n n n n Wherein the substituents have the following meanings:n n n R 1 , R 4 are independently C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 alkoxy, wherein Are optionally substituted with halogen), H, halogen, nitro, CN,n n n R 2 represents H, OH, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, wherein these groups are optionally substituted with halogen,n n n R 3 is C 1 -C 12 alkyl, C 3 -C 12 cycloalkyl, C 2 -C 12 alkenyl, C 5 -C 12 cycloalkenyl, C 2 -C 12 alkynyl, C 3 -C 12 cycloalkyl -C 1 -C 4 alkyl where these groups are optionally substituted with R 7 , phenyl, phenyl-C 1 -C 6 alkyl, phenyl-C 2 -C 6 alkenyl, phenyl-C 2 -C 6 Alkynyl, phenyloxy-C 1 -C 6 alkyl, phenyloxy-C 2 -C 6 alkenyl, phenyloxy-C 2 -C 6 alkynyl, wherein the alkyl moiety, alkenyl moiety and alkynyl moiety are Substituted with R 7 , the phenyl ring optionally substituted with R 5 ), -C (R 8 ) = NOR 6 , andn n n X represents O, S or a direct bond,n n n R 5 is H, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 4 alkoxy, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, wherein these groups are optionally Substituted with halogen), halogen, nitro, CN, phenyl (which may be substituted by R 1 ), phenoxy (which may be substituted by R 1 ), C 1 -C 6 alkyl-phenyl, wherein the alkyl moiety is optional Substituted with halogen, and the phenyl ring is optionally substituted with R 1 ),n n n R 6 is C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 2 -C 4 -alkenyl, C 2 -C 4 alkynyl, wherein these groups are optionally substituted with halogen, phenyl ( May be substituted with R 1 ),n n n R 7 is C 1 -C 4 alkyl, C 1 -C 8 alkoxy, C 2 -C 8 alkenyloxy, C 2 -C 8 alkynyloxy, C 1 -C 4 alkoxy-C 1 -C 8 alkoxy, wherein , These groups are optionally substituted with halogen), halogenn n n R 8 is H, R 7 or C 1 -C 12 alkyl, C 3 -C 12 cycloalkyl, C 2 -C 12 alkenyl, C 5 -C 12 cycloalkenyl, C 3 -C 12 cycloalkyl-C 1 -C 4 alkyl, wherein these groups are optionally substituted with halogen, phenyl (which may be substituted with R 5 ),n n n n represents 0-4,n n n m represents 0 and 1.n n n Also disclosed is the use of the trifluoromethyl-thiophene carboxylic acid anilide of the present invention as an antifungal agent and a formulation containing the trifluoromethyl-thiophene carboxylic acid anilide. |
| priorityDate | 2003-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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