Abstract:
The present invention relates to one of the two geometrical isomers (a compound defined as I-A isomer in the description below) of a triazole compound represented by the formula (I) or (II), ##STR1## wherein R.sub.1 is a hydrogen atom, a C.sub.1 -C.sub.4 alkyl, C.sub.3 -C.sub.4 alkenyl or 2-propynyl group, R.sub.2 is a C.sub.1 -C.sub.6 alkyl, cyclopropyl or 1-methylcyclopropyl group, R.sub.3, which may be the same or different, is a halogen atom, a C.sub.1 -C.sub.4 alkyl, halogen-substituted C.sub.1 -C.sub.3 alkyl, C.sub.1 -C.sub.4 alkoxy, phenoxy, phenyl, cyano or nitro group, n is an integer of 0 to 3, and the term, halogen, means chlorine, bromine and fluorine atoms, its salts, production thereof and a fungicide, herbicide and/or plant growth regulator for agriculture and horticulture containing said compound as an active ingredient.
Abstract:
Amide phosphorothiolate derivatives of the formula, ##STR1## wherein X is an oxygen or sulfur atom, Y is an oxygen or sulfur atom or imino group, R.sub.1 and R.sub.2, which may be the same or different, are each a C.sub.1 -C.sub.3 alkyl group, R.sub.3 is a C.sub.1 -C.sub.4 alkyl group, R.sub.4 is a hydrogen atom or methyl group, R.sub.5 is a C.sub.1 -C.sub.3 alkyl, methoxy or ethoxy group, Z is a hydrogen atom, a methyl group or chlorine atom and n is 1 or 2, a process for producing said derivatives characterized by reacting the salt of thiophosphoric ester represented by the formula, ##STR2## wherein X, Y, R.sub.1 and R.sub.2 are as defined above and M is a sodium or potassium atom or ammonium group, with a haloacetamide derivative of the formula, ##STR3## wherein R.sub.3, R.sub.4, R.sub.5, Z and n are as defined above and W is a halogen atom, and a combined insecticide, acaricide, nematocide and/or fungicide containing said derivatives as an active ingredient.
Abstract:
A fungicidal composition which comprises as an active ingredient a N-benzoylanthranilate compound of the formula, ##STR1## wherein X is a hydrogen or 3-halogen atom or a 3-methoxy, 4-methoxy, 2,4-dimethoxy, 3,4-dimethoxy, 3-halo-4-methoxy, 3,4-methylenedioxy or 3,5-dimethoxy group and R is a hydrogen atom or a C.sub.1 -C.sub.7 alkyl, C.sub.3 -C.sub.6 cycloalkyl, C.sub.2 -C.sub.4 alkenyl, halo-C.sub.1 -C.sub.3 alkyl, C.sub.1 -C.sub.4 alkoxy C.sub.1 -C.sub.4 alkyl or N,N-di-C.sub.1 -C.sub.2 alkylamino C.sub.1 -C.sub.4 alkyl group and an inert carrier, and their preparation and use as a fungicide.
Abstract:
1-Phenyl-2-azolyl-4,4-dimethyl-1-penten-3-ols of the formula: ##STR1## wherein X, which may be same or different, is an alkyl (C.sub.1 -C.sub.4), cyano, alkoxy (C.sub.1 -C.sub.4), phenoxy, phenyl group, halogen atom, n is zero or an integer of 1 to 2, A.sub.Z is an imidazole group of the formula ##STR2## or a triazole group of the formula ##STR3## and salt thereof, which show high fungicidal activities without any material toxicity to mammals and plants and can be produced by reacting the corresponding 3-ketone compound with a reducing agent.
Abstract:
1-Cycloalkylcarbonyl-3-(3,5-dihalophenyl)imidazolidine-2,4-diones of the formula: ##STR1## wherein X is a chlorine or bromine atom, R.sub.1 is a C.sub.3 -C.sub.6 cycloalkyl, tetramethylcyclopropyl, 2,2-dimethyl-3-isobutenylcyclopropyl or 2,2-dimethyl-3-dichlorovinylcyclopropyl group and R.sub.2 and R.sub.3 are individually a hydrogen atom or a methyl group, which show high fungicidal activities without any material toxicity to mammals and plants and which can be produced by reacting the corresponding 1-unsubstituted compound with a cycloalkanecarboxylic acid or a reactive derivative thereof.
Abstract:
Novel phosphorothioates represented by the formula, ##STR1## wherein R.sub.1 is a chlorine or bromine atom, R.sub.2 is methyl or ethyl group and R.sub.3 is a chlorine or bromine atom or nitro group, which have a low toxicity to men and beasts as well as fishes, no phytotoxicity to crops, excellent fungicidal effect on injurious epidemic soil fungi in agriculture, horticulture and the like, and a wide range of uses for prevention of soil epidemics to effect the growth promotion of crops.
Abstract:
N-substituted-aminoacetamide compounds having the formula (I) ##STR1## wherein R.sub.1 represents a lower alkenyl group having up to 5 carbon atoms, a halogen-substituted lower alkenyl group having up to 5 carbon atoms or a lower alkynyl group having up to 5 carbon atoms, R.sub.2 and R.sub.3, which may be the same or different, each represents a hydrogen atom or a lower akyl group having up to 4 carbon atoms, and the inorganic and organic acid addition salts thereof, which are useful as fungicidal agents, processesfor preparing N-substituted-aminoacetamide compounds and fungicidal compositions containing at least one compound of the formula (I) as an active inredient.
Abstract:
A compound of the formula: ##STR1## useful as a fungicidal agent against phytopathogenic fungi, particularly their strains resistant to benzimidazole and thiophanate fungicides and/or cyclic imide fungicides.
Abstract:
A compound of the formula: ##STR1## useful as a fungicidal agent against phytopathogenic fungi, and particularly against strains resistant to benzimidazole, thiophanate and/or cyclic imide fungicides.
Abstract:
A fungicidal composition containing as an active ingredient a mixture of a cyclic imide fungicide and a fungicide selected from O,O-dimethyl O-(2,6-dichloro-4-methylphenyl) phosphorothioate, 2,6-dichloro-4-nitroaniline and 1,4-dichloro-2,5-dimethoxybenzene in the ratio of 1:0.1 to 1:10 by weight in a total amount of 1 to 90% by weight, and an inert carrier or diluent.