Sumitomo Chemical Company, Limited

Kimitoshi Umeda

Noriyasu Sakamoto

Hiroaki Fujimoto

Hirosi Kisida

Akira Shuto

Noritada Matsuo

Kazunori Tsushima

Masaya Suzuki

Takao Ishiwatari

Taro Hirose

Hiroki Tomioka

Sanshiro Matsuo

Naoto Meki

Tomotoshi Imahase

Toshio Nagatomi

Hiroshi Kisida

Tadashi Ohsumi

Makoto Fujimura

Kazuya Ujihara

Tomoyuki Kusaba

Tsuguhiro Katoh

Norio Kimura

The dihalopropene compounds of the general formula (I) have excellent insecticidal/acaricidal activity, so that they are satisfactorily effective for the control of noxious insects, mites and ticks.

Dihalopropene compounds, insecticidal/acaridcidal agents containing same, and intermediates for their production

The dihalopropene compounds of the general formula &lsqb;I&rsqb; have excellent insecticidal/acaricidal activity, so that they are satisfactorily effective for the control of noxious insects, mites and ticks.

Dihalopropene compounds, insecticidal/acaricidal agents containing same, and intermediates for their production

The dihalopropene compounds of the general formula [I ] have excellent insecticidal/acaricidal activity, so that they are satisfactorily effective for the control of noxious insects, mites and ticks.

Dihalopropene compounds, insecticidal/acaricidal agents containing same,

The dihalopropene compounds of the general formula �I! have excellent insecticidal/acaricidal activity, so that they are satisfactorily effective for the control of noxious insects, mites and ticks.

There is disclosed a dihalopropene compound of the formula I: ##STR1## wherein l is an integer of 1 to 5; m is an integer of 1 to 4; R.sup.1 's and R.sup.2 's are the same or different and are independently halogen or various other groups; D is oxygen; X's are the same or different and are independently chlorine or bromine; Y is oxygen; Z, P and Q are the same or different and are independently nitrogen or CH, provided that P and Q are not simultaneously nitrogen, and when Y is sulfur, Z is CH. Also disclosed is an insecticide/acaricide comprising the dihalopropene compound as an active ingredient. The dihalopropene compound exhibits excellent insecticidal/acaricidal action. Further disclosed is an intermediate compound for use in the production of the dihalopropene compound.

Intermediate compound for use in production of dihalopropene compound

There is disclosed a dithiocarbonimide derivative of the formula: ##STR1## wherein B is a C.sub.1 -C.sub.6 alkyl group; X is an NH group or an oxygen atom and Y is a nitrogen atom or a CH group, A is a phenyl group, a heterocyclic group, an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, a cycloalkenyl group, a bicycloalkyl group or a tricycloalkyl group, all of which may be substituted. Also disclosed are a fungicidal/insecticidal/acaricidal agent containing the dithiocarbonimide derivative as an active ingredient, an intermediate for use in the production of the dithiocarbonimide derivative, and a process for producing the dithiocarbonimide derivative from the intermediate.

Dithiocarbonimide derivatives useful as acaricidal, fungicidal, and

Dihaloprene compound, insecticide/acaricide containing said

An amide derivative of the formula: ##STR1## which is useful for control of insect pests.

Amide derivatives, their production processes and their compositions for

A carbamic acid derivative of the formula: ##STR1## which is useful for the control of insect pests.

Carbamic acid derivatives, and their production and use

Aromatic compounds are disclosed of the formula: ##STR1## wherein R.sup.1 is a C.sub.3 -C.sub.8 alkyl group, a C.sub.3 -C.sub.8 alkoxy group, an alkoxyalkyl group having 3 to 8 carbon atoms, a C.sub.3 -C.sub.8 alkenyl group, a C.sub.3 -C.sub.8 alkenyloxy group, an alkenyloxyalkyl group having 3 to 8 carbon atoms, a C.sub.3 -C.sub.8 haloalkyl group, a C.sub.3 -C.sub.8 haloalkoxy group, a haloalkoxyalkyl group having 3 to 8 carbon atoms, a C.sub.3 -C.sub.8 haloalkenyl group, a C.sub.3 -C.sub.8 haloalkenyloxy group, a haloalkenyloxyalkyl group having 3 to 8 carbon atoms or a C.sub.3 -C.sub.8 alkynyloxy group; R.sup.2 is a halogen atom; R.sup.3 groups are the same or different and each is a hydrogen atom, a halogen atom or a methyl group; R.sup.4 is a hydrogen atom or a methyl group; R.sup.5 groups are the same or different and each is a hydrogen atom, a halogen atom, a C.sub.1 -C.sub.4 alkyl group, a C.sub.1 -C.sub.4 haloalkyl group, a C.sub.1 -C.sub.4 alkoxy group, a C.sub.1 -C.sub.4 haloalkoxy group, a C.sub.1 -C.sub.4 alkylthio group, a C.sub.1 -C.sub.4 haloalkylthio group, a 3,4-methylenedioxy group, a methoxymethyl group, a cyano group or a nitro group; m is an integer of 1 to 3; and n is an inter of 1 to 5. These compounds are useful for the control of insect pests.

Aromatic compounds, their production processes and their compositions

The present invention relates to certain novel amide compound represented by the formula of ##STR1## wherein A is an oxazole and, X, R.sup.1, R.sup.2, R.sup.3, R.sup.4, Y, the ring B, R.sup.5, R.sup.6, l and m are the same as defined in the present specification, its production and an insecticidal and/or acaricidal composition containing it as an active ingredient.

Amide compound and its production and use

An aromatic compound of the formula: ##STR1## wherein R.sup.1 is a C.sub.3 -C.sub.8 alkyl group, a C.sub.3 -C.sub.8 alkoxy group, an alkoxyalkyl group having 3 to 8 carbon atoms, a C.sub.3 -C.sub.8 alkenyl group, a C.sub.3 -C.sub.8 alkenyloxy group, an alkenyloxyalkyl group having 3 to 8 carbon atoms, a C.sub.3 -C.sub.8 haloalkyl group, a C.sub.3 -C.sub.8 alkoxy group, a haloalkoxyalkyl group having 3 to 8 carbon atoms, a C.sub.3 -C.sub.8 haloalkenyl group, a C.sub.3 -C.sub.8 haloalkenyloxy group, a haloalkenyloxyalkyl group having 3 to 8 carbon atoms or a C.sub.3 -C.sub.8 alkynyloxy group; R.sup.2 is a halogen atom; R.sup.3 is, the same or different, a hydrogen atom, a halogen atom or a methyl group; R.sup.4 is a hydrogen atom or a methyl group R.sup.5 is, the same or different, a hydrogen atom, a halogen atom, a C.sub.1 -C.sub.4 alkyl group, a C.sub.1 -C.sub.4 haloalkyl group, a C.sub.1 -C.sub.4 alkoxy group, a C.sub.1 -C.sub.4 haloalkoxy group, a C.sub.1 -C.sub.4 alkylthio group, a C.sub.1 -C.sub.4 haloalkylthio group, a 3,4-methylenedioxy group, a methoxymethyl group, a cyano group or a nitro group; m is an integer of 1 to 3; and n is an integer of 1 to 5. These compounds are useful for the control of insect pests.

Growing community of inventors

Toyonaka, Japan

Kimitoshi Umeda