Nihon Tokushu Noyaku Seizo K.k.

Nihon Bayer Agrochem, K.k.

Shinji Sakawa

Yoshio Kurahashi

Junichi Saito

Kozo Shiokawa

Shinzo Kagabu

Yasuo Yamada

Koichi Moriya

Tatsuo Tamura

Toyohiko Kume

Kunihiro Isono

Noboru Matsumoto

Shinichi Tsuboi

Yumi Hattori

Shoko Sasaki

Toshihito Kondo

Osamu Katsumata

Toshio Gotoh

Substituted benzylcycloalkenylurea derivatives of the formula (I) ##STR1## wherein X represents a halogen atom or a lower alkyl group, Y represents an oxygen atom or a sulfur atom,

Substituted benzylcycloalkenylamines and carbamoylhalide intermediates

Novel fungicidally active N-benzyl-cyclopropanecarboxamides of the formula ##STR1## wherein X=represents halogen,

N-benzyl-cyclopropanecarboxamide fungicides

Novel fungicidally active N-benzyl-cyclopropanecarboxamides of the formula ##STR1## wherein X represents halogen,

Novel N-benzyl-cyclopropanecarboxamide fungicides

Substituted benzylcycloalkenylurea derivatives

An insecticidal and fungicidal composition comprising (1) An insecticidally effective amount of a nitromethylene derivative of the formula ##STR1## in which X is a lower alkyl group, a lower alkoxy group, or a halogen atom,

Insecticidal and fungicidal composition for agricultural and

Novel carbamoylimidazole derivatives of the formula (I) ##STR1## in which R.sup.1 represents lower alkyl, lower alkoxy-lower alkyl or cycloalkyl having 3 to 8 carbon atoms,

Carbamoylimidazole derivatives

This invention relates to 2,2-dichloro-3,3-dimethylcyclopropylmethylamine, a novel compound which is useful as an agricultural and horticultural fungicide or as a synthetic intermediate for other cyclopropyl derivatives and other compounds, and to a process for production thereof.

2,2-dichloro-3, 3-dimethylcyclopropylmethylamine

Carbamoylimidazole derivatives and fungicidal use thereof

The invention relates to new trichloroacryloyl oxime compounds of the general formula (I) ##STR1## wherein each of R.sup.1 and R.sup.2 represents a hydrogen atom, a lower alkyl group, a benzyl group, a benzylthio group, a lower alkylthio group, a cycloalkyl group, a halogen atom, a styryl group, a halogenophenylthio group, a naphthyl group, or a phenyl group which may optionally be substituted by at least one substituent selected from the class consisting of a halogen atom, a nitro group, a lower alkyl group, a lower alkoxy group, a phenoxy group, a benzyloxy group, a lower alkylthio group, a thiocyanato group, a di-lower alkylamino group, a halogenopyridyloxy group and a methylenedioxy group, or R.sup.1 and R.sup.2, together with the carbon atom to which they are bonded, may form an aliphatic ring, said ring being optionally substituted by at least one methyl group, and their use as fungicides. They may be obtained by reacting a trichloroacryloyl halide with an oxime, or by reacting a salt of trichloroacryloyl acid, a formic acid ester halide and an oxime, if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.

Trichloroacryloyl oxime fungicides

Fungicidally active novel benzylurea derivatives of the formula ##STR1## in which R.sup.1 is a halogen atom or a lower alkyl group,

Growing community of inventors

Tokyo, Japan

Shinji Sakawa