http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3704112-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_634538388f2dd27ea0a8bc2a2032c517 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-50 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D251-50 |
| filingDate | 1969-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1972-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea8281827a48c4bf703338d6000f76a9 |
| publicationDate | 1972-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-3704112-A |
| titleOfInvention | Trisubstituted-s-triazine chloroacetaldehyde adducts useful as herbicides |
| abstract | NOVEL ADDUCTS OF 2-ALKYLAMINO-4-AMINO-6-CHLORO-S-TRIAZINES WITH CHLOROACETALDEHYDES ARE PREPARED BY REACTING THE AMINO SUBSTITUTED-S-TRIAZINE WITH DI- OR TRICHLOROACETALDEHYDE IN AN INERT SOLVENT. REACTION TEMPERATURES OLF 40 TO 100* C. FOR ONE-HALF TO ONE HOUR ARE PREFERRED. THE REACTION MIXTURE MAY BE COOLED TO SEPARATE THE PRODUCT; EVAPORATION OF THE SOLVENT AT ADVANCED TEMPERATURES SHOULD BE AVOIDED AS THIS MAY FORM UNDESIRABLE BY-PRODUCTS. THE PRODUCTS ARE HIGHLY SELECTIVE HERIBICIDES. THE COMPOUND 2-CHLORO-4- (1-HYDROXY-2,2,2-TRICHLOROETHYLAMINO)-6-ISOPROPYLAMINO-S-TRIAZINE IS PARTICULARLY USEFUL BECAUSE IT WILL SELECTIVELY DESTROY WEEDS IN BOTH CORN AND OAT CROPS, MAKING POSSIBLE AN INITIAL CROP OF CORN IMMEDIATELY FOLLOWED BY AN OAT CROP. |
| priorityDate | 1969-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 52.