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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C333-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-42
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-42
filingDate 1971-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bd31b3ea2babc29ea3dc34fa2e85a993
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0c81bf9113c955704547d828afc920d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c96b026f3226b8035fa1809c02e65da
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76cdf5e7804539ca6a287d37d397139e
publicationDate 1973-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2144125-A1
titleOfInvention DITHIOCARBAMIC ACID SALT OF UREA DERIVATIVES, PROCESS FOR THEIR PRODUCTION AND THEIR FUNGICIDES AND MICROBICIDAL USE
abstract Cpds. of gen. formula (I):- where R and R'= H, methyl or ethyl; R' may also be:- A = alkylene (max 4C); R + R' + N may form a 5-6-membered heterocyclic ring opt. contng. -O and/or -N; B = NH-R", or O-R"; R" = H, alkyl (is not >20C), cycloalkyl (is not >6C) or aryl opt. substd. with lower alkyl, nitro and/or halogen; n = 1 when R' = H, methyl or ethyl; n = 2 when R' = are prepd. by reacting a cpd. (II): or its mineral salts, with a cpd. (III):- or its mineral salts; where R and R"' = H, methyl or ethyl; R"' may also be M = ammonium or alkalimetal; R + R"' + N = as signified for R + R' + N; in the presence of polar solvents pref. at 10-80 degrees C. (I) are esp. active against Phytophtora intestans and Fusicladium dendriticum, and also have microbicidal activity against a wide range of partly pathogenic micro-organisms. They are also active against blue- and green algae.
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priorityDate 1971-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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