http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-1643617-B2
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-18 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-27 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-292 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C35-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-095 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-27 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-29 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C35-20 |
| filingDate | 1967-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1974-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | DE-1643617-B2 |
| abstract | 1,153,468. Cyclooctyl formate. ASPRONICHOLAS Ltd. 13 Dec., 1967 [22 Dec., 1966], No. 57429/66. Heading C2C. The invention comprises cyclooctyl formate. It may be prepared by reacting cyclooctene with formic acid, preferably at a temperature between 50‹ and 85‹ C. in the absence of a catalyst. Cyclooctyl formate may be converted to cyclooctanol by hydrolysis of the acyl group preferably by the action of an aqueous solution of an alkali metal hydroxide. The cyclooctanol so obtained may be oxidized to cyclooctanone by, for example, treating with chromic acid or, alternatively the cyclooctyl formate may be converted directly to cyclooctanone by treating with chromic acid. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0048804-A1 |
| priorityDate | 1966-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 45.