http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1431238-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02A50-30 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-045 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-045 |
| filingDate | 1974-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1976-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1431238-A |
| titleOfInvention | Microbicidal agents and their use |
| abstract | 1431238 Substituted benzyl alcohols BAYER AG 2 July 1974 [3 July 1973] 29245/74 Heading C2C [Also in Division A5] Benzyl alcohols of the general formula in which R<SP>1</SP> is a hydrogen, fluorine, chlorine, bromine, trifluoromethyl, trifluoromethoxy or trifluoromethylthio radical; and R<SP>2</SP> is a fluorine, chlorine, bromine, trifluoromethyl, trifluoromethoxy or trifluoromethylthio radical are prepared (a) from the corresponding benzaldehydes by catalytic reduction, (b) from the corresponding carboxylic acids by reduction with LiAlH 4 or (c) from the corresponding carboxylic acid halides by reduction with NaBH 4 . Exemplified are the preparation of 2,4- difluorobenzyl alcohol, 3-ohloro-4-trifluoromethoxy benzyl alcohol, 2-fluoro-4-chloro benzyl alcohol, 2-fluoro-6-chloro benzyl alcohol, 2- trifluoromethyl benzyl alcohol, 2-chloro-4-trifluoromethyl benzyl alcohol and 4-trifluoromethylthio benzyl alcohol. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-2122900-A |
| priorityDate | 1973-07-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 37.