PROCESS FOR OBTAINING THIAZOLYLIDENE - OXO -PROPIONITRILE

Oxopropionitrile derivs. of formula (I) are new, (where R1 = H, halo, 1-6C alkyl, 3-6C cycloalkyl, thienyl, pyridyl or aromatic hydrocarbyl substd. by one or more independently chosen halo, 1-4C alkyl, 1-4C alkoxy 1-4C alkylthio, trifluoromethyl, nitro or cyano groups; R2 = H, halo, 1-6C alkyl, 3-6C...

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Bibliographic Details
Main Authors BUEHMANN U, JOPIEN H, PUTTNER R
Format Patent
LanguageEnglish
Published 31.12.1986
Edition2
Subjects
AGRICULTURE
ANIMAL HUSBANDRY
BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES
CHEMISTRY
FISHING
FORESTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HUNTING
METALLURGY
ORGANIC CHEMISTRY
PEST REPELLANTS OR ATTRACTANTS
PLANT GROWTH REGULATORS
PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF
TRAPPING
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Summary:Oxopropionitrile derivs. of formula (I) are new, (where R1 = H, halo, 1-6C alkyl, 3-6C cycloalkyl, thienyl, pyridyl or aromatic hydrocarbyl substd. by one or more independently chosen halo, 1-4C alkyl, 1-4C alkoxy 1-4C alkylthio, trifluoromethyl, nitro or cyano groups; R2 = H, halo, 1-6C alkyl, 3-6C cycloalkyl, thienyl, pyridyl, phenyl or aromatic hydrocarbyl substd. by one or more independently chosen halo, 1-4C alkyl, 1-4C alkoxy, 1-4C alkylthio, trifluoromethyl, nitro or cyano groups and R3 = aromatic hydrocarbyl opt. substd. by one or more independently chosen halo, 1-4C alkyl, 1-4C halo alkyl, 1-4C alkoxy, trifluoromethyl, nitro or cyano groups). The cpds. are usually used at concentrations of 0.005-5.0%, pref. 0.01-0.5%.
Bibliography:Application Number: YU19800001163