http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0114575-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-30
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-48
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54
filingDate 1983-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1d6f263883bbfea00c55f3379ce2f33
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aba0eabb859ca6dd8c2b2ee93fe61bf9
publicationDate 1984-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0114575-A1
titleOfInvention 2,4-Diamino-6-halogen-5-trifluoromethyl pyrimidine with herbicidal activity
abstract 2,4-diamino-6-halogen-5-trifluoromethylpyrimidines of the formula wherein X is a halogen atom, especially chlorine or fluorine; R 1 and R 2 each independently represent hydrogen, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl or together a C a -C 7 alkylene bridge, have extremely selective herbicidal properties and are suitable for controlling weeds in crops of useful plants like corn, grain or soy. They are prepared by aminating 2,4,6-trihalogen-5-trifluoromethylpyrimidine, which in turn can be obtained by fluorinating 2,4,6-trihalopyrimidine-5-carboxylic acid. The 2,4,6-trihalogen-5-carboxylic acids are new intermediates and are obtained by oxidation in sulfuric acid using chromium trioxide of 2,4,6-trihalogen-5-methyl-, halomethyl- or -formylpyrimidine.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101140695-B1
priorityDate 1982-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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