Sankyo Company, Limited

Murata Manufacturing Co., Ltd.

Sanyo Co., Ltd.

Hiroshi Ohta

Hideo Takeshiba

Junzo Tobitsuka

Shigehiro Kato

Hiroyuki Itoh

Hiroshi Yasuda

Kazuo Sato

Yuichi Takaoka

Toshiyuki Konosu

Takayo Katsuki

Sadao Oida

Noriko Takeda

Kiyofumi Torii

Hisaki Kajino

Yukiyoshi Takahi

Shinji Omura

Yasuhiko Kondo

Osamu Watanabe

Chiaki Imai

Akira Toba

Kouichi Tatsuoka

Masaru Nakagawa

Masahiro Yokota

A thermistor for surface mounting includes a first conductive terminal member, a case having a top opening, a planar thermistor element having electrodes on mutually opposite main surfaces thereof, and a second conductive terminal member having at one end thereof a planar cover part which is attached to the top part of the case. One end of the first terminal member is positioned inside the case and above its bottom member. The other ends of the first and second terminal members are positioned on the bottom surface of the case.

Electronic apparatus and surface mounting devices therefor

Compounds of formula (I): ##STR1## �wherein: R.sup.1 represents halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, cycloalkyl, or cycloalkyloxy; R.sup.2 represents hydrogen or halogen; R.sup.3 represents hydrogen, alkyl, or cycloalkyl; and the dotted line represents a single or double carbon--carbon bond!; and salts thereof have valuable fungicidal activities which make them of considerable value in agriculture and horticulture.

Tricyclic compounds having fungicidal activity, their preparation and

Compounds of formula (I): ##STR1## wherein: A is 1,2,4-triazol-1-yl or imidazol-1-yl; n is 0, 1, 2 or 3; X is halogen, phenyl, alkyl, haloalkyl, alkoxy, or haloalkoxy, or (X).sub.n is alkylenedioxy; R.sup.1 is alkyl or phenyl; and R.sup.2 and R.sup.3 are each alkyl; and salts thereof have valuable anti-fungal activity. Certain intermediates in the preparation of these compounds are also disclosed.

Fungicidal silicon-containing compounds and their agrochemical and

Compounds of formula (I): ##STR1## [in which: R.sup.1 and R.sup.2 are hydrogen or alkyl, or together are cycloalkyl; R.sup.3 and R.sup.4 are hydrogen, alkyl or phenyl, or together are cycloalkyl; or R.sup.1 and R.sup.3 together are cycloalkyl fused to the oxetane ring; Ar is phenyl substituted by R.sup.5, R.sup.6 and R.sup.7, where R.sup.5, R.sup.6 and R.sup.7 are hydrogen, halogen, alkyl, alkoxy, halogenated alkyl or halogenated alkoxy; and R.sup.8 and R.sup.9 are hydrogen or alkyl] and salts thereof have valuable agricultural and pharmaceutical anti-fungal or fungicidal activity. They may be prepared by a variety of processes.

Oxetane derivatives and their use as anti-fungal or fungicidal agents

Growing community of inventors

Shiga, Japan

Hiroshi Ohta