Nec Corporation

Kureha Corporation

Kureha Chemical Industry Company, Limited

Teac Corporation

Sumitomo Mitsubishi Silicon Corporation

Nihon Micro Coating Co., Ltd.

Sumco Corporation

Unisis Corporation

Ntt Advanced Technology Co., Ltd.

Nihon Micron Coating Co., Ltd.

Toru Yamazaki

Mikiro Yanaka

Hiroyuki Enari

Taiji Miyake

Toshikazu Dewa

Michihito Ise

Hisashi Kanno

Fuyuhiko Nishijima

Nobuyuki Araki

Hiroshi Maruoka

Nobuyuki Kusano

Masaru Mori

Kunitaka Hirose

Eiyu Imai

Shigeyuki Kikumoto

Ryo Matsui

Hiroshi Takahashi

Shigeru Suzuki

Masahiro Ono

Ryo Harigae

Emiko Obata

Atsushi Saitou

Atsushi Ito

Yoshiro Aoki

Kenji Aoki

Naoki Yamamoto

Koichi Niimura

Akihiko Endo

Haruka Takahashi

Sei Kumakura

Yoshiyuki Takemura

Kazuhiko Sunagawa

Osamu Murata

Koju Watanabe

Yoshio Murakami

Izuru Morioka

Mikio Sugano

Takehiro Watanabe

Hideya Saitoh

Tetsuya Baba

Naoyuki Hamada

Tsutomu Mukade

Chiemi Kojima

Shingo Konno

A method by which an intermediate product of an azole derivative can be produced at a lower cost than known production methods is provided. A method for producing a compound represented by General Formula (IV) includes converting a compound represented by General Formula (II) into the compound represented by General Formula (IV) using (a) dimethyl sulfide and/or dimethyl sulfoxide, and (b) a methyl-LG (an LG is a nucleophilically substitutable leaving group and is selected from the group consisting of a halogen group, an alkoxysulfonyloxy group, an aryloxysulfonyloxy group, an alkylsulfonyloxy group, a haloalkylsulfonyloxy group, and an arylsulfonyloxy group) in the presence of an inorganic base.

Method for producing compound

It is provided a plant disease controlling agent having low toxicity to human and animals and excellent handling safety, and showing excellent controlling effects on various plant diseases and high antibiotic action to plant disease germs. A compound represented by the following the general formula (I), or an N-oxide or agrochemically acceptable salt thereof. 

Azole derivative, intermediate compound, method for producing azole derivative, agricultural or horticultural chemical agent, and protective agent for industrial material

An electronic device with faders. In order to enable a user to readily ascertain which of a plurality of faders belongs to the same group and which one of the faders in the group is a master fader, indicators of all of the faders in the group are lighted when the thus-set master fader in the grouped faders is operated. When the user operates slave faders, the operation is revoked, and only the indicator corresponding to the master fader is lighted or blinked.

Method of operating an electronic device with a master fader and a plurality of slave faders

In order to produce an intermediate from which a cyclic alcohol compound can be stereoselectively obtained, a method for producing an oxetane compound according to the present invention includes the step of reacting, with a cyanide salt, a compound represented by Formula (I): wherein Ris selected from a hydrogen atom and an alkyl group optionally having a substituent; Xis selected from a halogen atom and &#x2014;OSORwhere Ris selected from an alkyl group optionally having a substituent, a phenyl group, and a naphthyl group; and a ring Z1 represents a cyclic hydrocarbon optionally having a substituent, 

Method for manufacturing oxetane compound, method for manufacturing azolylmethylcyclopentanol compound, and intermediate compound

In order to provide a compound that shows a strong effect on controlling a plant disease, a triazole compound of the present invention (i) is a compound in which &#x2014;OH group, &#x2014;Rgroup, and CH&#x2014;Ar group are bonded in cis configuration with a cyclopentane, (ii) is (&#x2212;)-enantiomer or (+) enantiomer, and (iii) is represented by Formula (I): 

Triazole compound and use thereof

In order to provide a novel azole derivative, an azole derivative of the present invention is an azole derivative represented by a general formula (V'). (where Rand Rindependently represent a hydrogen atom, a C-Calkyl group, a phenyl group, or a benzyl group; X represents a halogen atom, a C-Calkyl group, a haloalkyl group, an alkoxy group or a haloalkoxy group, a phenyl group, a cyano group, or a nitro group; m represents an integer of 0 to 5; and A represents a nitrogen atom or a methyne group.)

Azole derivative, method for producing azole derivative, and intermediate compound

Electronic device with a master fader and a plurality of slave faders

The present invention is to provide a method of producing a carbonyl compound at a higher yield. The method of producing a carbonyl compound according to the present invention produces a carbonyl compound represented by general formula (I) by subjecting a compound represented by general formula (II) to dealkoxycarbonylation in the presence of a hydrogen halide salt of tertiary amine.  In the formula, R represents an alkyl group having from 1 to 4 carbons.

Production method of carbonyl compound

A method of producing an azole derivative according to the invention represented by Formula (XI)  wherein Rdenotes a C-Calkyl group, a C-Calkenyl group or a C-Calkynyl group; Rdenotes a C-Calkyl group; each Y denotes a halogen atom, a C-Calkyl group, a C-Chaloalkyl group, a C-Calkoxy group, a C-Chaloalkoxy group, a phenyl group, a cyano group or a nitro group; and m denotes 0 to 5; when m is 2 or more, each Y may be the same or different. As a result, an azole derivative contained as an active ingredient in an agro-horticultural agent having an excellent controlling effect on diseases can be provided.

Azole derivatives, methods for producing the same, intermediate thereof, agro-horticultural agents

An azole derivative according to the invention is represented by Formula (XI) wherein Rdenotes a C-Calkyl group, a C-Calkenyl group or a C-Calkynyl group; Rdenotes a C-Calkyl group; each Y denotes a halogen atom, a C-Calkyl group, a C-Chaloalkyl group, a C-Calkoxy group, a C-Chaloalkoxy group, a phenyl group, a cyano group or a nitro group; and m denotes 0 to 5; when m is 2 or more, each Y may be the same or different. As a result, an azole derivative contained as an active ingredient in an agro-horticultural agent having an excellent controlling effect on diseases can be provided.

Provided is an ester of 3-[(4-dipropylamino-butyl)(4-{[(1H-imidazole-2-ylmethyl)(1-methyl-1H-imidazole-2-ylmethyl)amino]methyl}benzyl)amino]propionic acid which is easily hydrolyzed in serum. The amine compound of the present invention is an ester compound represented by general formula (1). (In general formula (1), n is 1-4, and Rand Rrepresent an alkyl group having 1-3 carbon atoms.) 

Amine compound and use for same

An azole derivative according to the invention is represented by Formula (I), wherein each of Rand Rdenotes a hydrogen atom, or a C-Calkyl group, a C-Calkenyl group or a C-Calkynyl group; Rand Rmay be substituted with Xor Xwhich is a halogen atom; each of nand ndenotes 0 or the number of X- or X-substituted hydrogen atoms among the hydrogen atoms in Ror R; each Y denotes a halogen atom, a C-Calkyl group, a C-Chaloalkyl group, a C-Calkoxy group, a C-Chaloalkoxy group, a phenyl group, a cyano group or a nitro group; m denotes 0 to 5; and A denotes a nitrogen atom or a methyne group. As a result, an azole derivative contained as an active ingredient in an agro-horticultural agent having an excellent controlling effect on diseases can be provided. 

Body pressing surfaces of A and B members at which a body of the packing is to be pressed come into contact with the body of the packing, and the body starts to be pressed. Then, projections of the packing are pressed with a delay from the pressing of the body because of gaps provided between the projections of the packing and projection-pressing surfaces at which the projections of the packing are to be pressed.

Catheter connector

It is intended to provide novel amine compounds which are efficacious against diseases such as infection with HIV virus, rheumatism and cancer metastasis. Namely, amine compounds represented by the following general formula (1):  In a typical case, A1 and A2 represent each an optionally substituted monocyclic or polycyclic aromatic heterocycle; W represents cyclic C3-10 alkylene, an optionally substituted monocyclic or polycyclic aromatic heterocycle, a monocyclic or polycyclic aromatic ring or a partly saturated polycyclic aromatic ring; X represents O, CH2, C(&#x2550;O) or NR11; and D is a group represented by the following general formula (4) or (6).  In the formula (6), Q represents a single bond, S, O or NR12; and Y is a group represented by the following general formula (7). z represents an optionally substituted monocyclic or polycyclic aromatic ring. In the formula (6), B represents NR25R26. In the above formulae, R1 to R26 each represents hydrogen, alkyl, alkenyl or alkynyl.

Amine compound and use thereof

A hard crystal substrate such as a GaN substrate or a SiC substrate is polished by using polishing oil slurry having abrading particles of artificial diamond clusters dispersed in a dispersant. The artificial diamond clusters include approximately spherical agglomerate particles with average particle size D50 of 20 nm or more and 50 nm or less, having primary particles with particle diameters of 2 nm or more and 10 nm or less. A rough polishing process is carried out first such that an average surface roughness of 0.5 nm or more and 1 nm or less is obtained, followed by a finishing process such that the average surface roughness of said surface becomes 0.2 nm or less.

Method of polishing hard crystal substrate

Growing community of inventors

Tokyo, Japan

Toru Yamazaki