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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-36
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-36
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filingDate 1968-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c73a7b13ebd730a552592a772c781ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a77caa86bcecb630d11acd9c90cc2b5
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publicationDate 1971-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-502762-A
titleOfInvention New herbicidal agent containing thiadiazolyl ureas
abstract 5 mercapto 1,3,4 thiadiazol 2 yl ureas with herbicidal activity. G5-. Are new cpds. of formula (I) (where R1 is a C1-6 aliphatic or cycloaliphatic, satd. or unsatd. hydrocarbon residue opt. with ether-type substitution or substd. by halogen, R2 is H or a C1-6 aliphatic or cycloaliphatic hydrocarbon residue, R3 is H or C1-6 alkyl and R4 is C1-10 alkoxy or an aliphatic or cycloaliphatic, satd. or unsatd. hydrocarbon residue opt. with ether-type substitution or substd. by halogen). The cpds. are herbicides and can be used for pre- or post-emergence control of mono- and dicotyledonous weeds. They can be used in high concns. as total herbicides and in lower concns. as selective herbicides. (I) may be prepd. e.g. by reacting (II) with a halocarbonic acid ester or COCl2 in the presence of an acid-binding agent and reacting the resulting carbamic acid deriv. with (III).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2719810-A1
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priorityDate 1968-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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