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filingDate 1982-04-22^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1984-05-15^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c46d35b17db075b431921157b4cd55db
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_374cf2c3c5052af0bafe929e0f9682e5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6ceadd3e550b0ce51b9f633d1101501
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c630c5c94a742683e6b6be0f71300142
publicationDate 1984-05-15^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4448773-A
titleOfInvention Microbicidal N-alkoxycarbonyl-alkyl-N-substituted acetyl-anilines and -naphthylamines
abstract Compounds of the formula ##STR1## in which Ar is 2-alkyl-, -alkoxy- or -halo-methyl-phenyl or α-naphthyl, each of which is further substituted, n R 1 is 2-furyl, 2-tetrahydrofuryl, alkenyl, cyclopropyl, β-alkoxyethyl, hydroxymethyl, triazolylmethyl, imidazolylmethyl, pyrazolylmethyl, alkylsulfinyl, alkylsulfonyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, alkenylthio, alkynylthio, alkylsulfinyloxy, dialkylaminosulfinyloxy, phosphoric or thiophosphoric esters or amides, or alkylcarbonyloxy, n R 7 is hydrogen or optionally-substituted methyl or ethyl, and n R 8 is alkyl optionally substituted by alkoxy, n are microbicidally, in particular fungicidally, active. Preferred compounds are those in which Ar is 2-methylphenyl, 2-methoxyphenyl, 2-chlorophenyl or α-naphthyl, each of which is further substituted by azido, and each of R 7 and R 8 is methyl.
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priorityDate 1981-04-29^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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