http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4486612-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_af99df08b153738cd418446a75d09bfc |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-275 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-124 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C33-46 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-124 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-275 |
filingDate | 1983-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1984-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_122987003289dc7cb9562ce37ea4b67e |
publicationDate | 1984-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-4486612-A |
titleOfInvention | Method of preparing tertiary carbinols |
abstract | Tertiary carbinols are prepared by reacting an appropriate tertiary halide with water in the presence of a catalytic amount of an emulsifying agent. α-Methyl-α-(2,2,2-trichloroethyl)benzyl alcohol is prepared with a high rate of conversion and a low incidence of the formation of an olefin by-product. α-Methyl-α-(2,2,2-trichloroethyl)benzyl alcohol is useful as a nitrification inhibitor and as an intermediate in the preparation of structurally related nitrification inhibitors. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5056981-A |
priorityDate | 1983-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 58.