http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1427554-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-56 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78 |
| filingDate | 1973-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1976-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1427554-A |
| titleOfInvention | Fungicidal agents |
| abstract | 1427554 2-Thiazolone-5-carboxylic acid esters BAYER AG 26 Oct 1973 [28 Oct 1972] 49937/73 Heading C2C [Also in Division A5] 2 - Thiazolone - 5 - carboxylic acid esters of the formula wherein R<SP>1</SP> is H, C 1 -C 12 alkyl optionally substituted by phenyl optionally substituted by one or more halogen atoms of C 1 -C 3 alkyl groups, C 5 -C 6 cycloalkyl or C 6 -C 10 aryl optionally substituted by one or more halogen atoms or C 1 - C3 alkyl groups; R<SP>2</SP> is C 5 -C 6 cycloalkyl, C 1 - C 18 alkyl optionally substituted by C 5 -C 6 cycloalkyl, C 1 -C 4 alkoxy, phenoxy, nitrile, C 1 -C 6 alkoxycarbonyl, or phenyl optionally substituted by one or more halogen atoms or C 1 -C 3 alkyl groups; and R<SP>3</SP> is H, C 5 -C 6 cycloalkyl, C 1 -C 18 alkyl optionally substituted by C 5 -C 6 cycloalkyl, C 1 -C 4 alkoxy, phenoxy, nitrile, C 1 -C 6 alkoxycarbonyl, phenyl optionally substituted by one or more halogen atoms or C 1 -C 3 alkyl groups, or as trihalomethyl, C 1 -C 6 alkoxycarbonyl or C 6 -C 10 aryl optionally substituted by one or more halogen atoms or C 1 -C 3 alkyl groups are prepared by reacting #-amino acrylic acid esters of formula wherein R<SP>1</SP>, R<SP>2</SP> and R<SP>3</SP> are as defined above, with chlorocarbonylsulphenyl chloride. The preparations of 3-benzyl-4-methyl-2-thiazolone- 5-carboxylic acid ethyl ester, 4-methyl-2-thiazolone-5-carboxylic acid cyclohexyl ester and other esters of Formula I are described in the examples. The esters are fungicides and may be used in fungicidal compositions (see Division A5). |
| priorityDate | 1972-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 18.