Mitsui Toatsu Chemicals, Incorporated

Mitsui Chemicals, Inc.

Yukihiro Yoshikawa

Akihiro Yamaguchi

Kenichi Sugimoto

Keizaburo Yamaguchi

Yoshimitsu Tanabe

Hiroyuki Katsuta

Kanji Tomiya

Yuji Yanase

Hideo Kawashima

Shunichi Inami

Junro Kishi

Naofumi Tomura

Osamu Takahashi

Shinji Takenaka

Hitoshi Shimotori

Kunihiro Yamada

Teruo Hirayama

Tooru Hihara

Tsutomu Ishii

Ryuichi Mita

Hiroyuki Itoh

Yoshitsugu Kono

Katsutoshi Ishikawa

Midori Yamazaki

Isao Kikuchi

Hiroharu Tanikawa

Kazunori Kawahara

Jun Kitagawa

Sunao Maeda

Yuji Yanese

Toshio Kitajima

Hideo Kawasima

A substituted anilide derivative represented by the formula (2): ##STR1## wherein A and B are methyl, and X is a hydrogen atom. The substituted anilide can be used to prepare a substituted carboxanilide derivative that exhibits a disease control effect against Botrytis cinerea, Powdery mildew, Pyricularia oryzae of rice plant and other various plant diseases, is excellent in residual effect, has activity against strains that are resistant to conventional chemicals, is safe for crops, and thus is useful as a plant disease control agent.

Substituted anilide derivative

A substituted carboxanilide derivative represented by the formula (1): ##STR1## wherein A is a hydrogen atom or methyl, B is a methyl or ethyl, and Het is 1-methyl-3-substituted-4-pyrazolyl or 2-methyl-4-substituted-5-triazoyl group, exhibits a disease control effect against Botrytis cinerea, Powdery mildew, Pyricularia oryzae of rice plant and other various plant diseases, is excellent in residual effect, has also activity against resistant strain for conventional chemicals, particularly exerts control effects against Botrytis cinerea at a lower dosage as compared with a prior art, is also safe for crops, and thus is useful as a plant control agent.

Substituted carboxanilide derivative and plant disease control agent

A novel substituted thiophene derivatives represented by the formula (1) in the invention: ##STR1## wherein R is a straight or branched alkyl group having 3-12 carbon atoms, straight or branched halogenoalkyl group having 3-12 carbon atoms, straight or branched alkenyl group having 3-10 carbon atoms, straight or branched halogenoalkenyl group having 3-10 carbon atoms, or cycloalkyl group having 3-10 carbon atoms, the cycloalkyl group being unsubstituted or substituted with an alkyl group having 1-4 carbon atoms, R and --NHCOAr are adjacent to each other, and Ar is a heterocyclic group; have excellent control activity on various plant disease such as Gray mold, Powdery mildew, Blast and Rust, and are useful as a plant disease control agent due to outstanding residual effect on Botrytis cinerea and excellent effect on Gibberella zeae.

Substituted thiophene derivative and plant disease control agent

The substituted thiophene derivative of the invention which is represented by the general formula (1) has a broad disease spectrum for a pathogenic fungus of various crops, exhibits an excellent controlling effect on disease such as gray mold, powdery mildew and rust in particular, and is also effective for a resistant fungus of conventional fungicides which has become a serious problem, and consequently is useful for an agricultural and horticultural fungicide. ##STR1##

Substituted thiophene derivative and agricultural and horticultural

Concentration process of gaseous chlorine

Pyrimidinyloxy(thio)quinoline derivatives represented by the formula (I) which exhibit an excellent controlling effect for plant diseases and are also safe for crop plants, preparation processes of the derivatives, and agri-horticultural fungicides comprising the derivatives as an active ingredient, are disclosed. ##STR1## In the formula (I), X is an oxygen atom or sulfur atom, Y is a hydrogen atom or halogen atom, Z is a hydrogen atom or methyl, R.sup.1 and R.sup.2 are methoxy or methyl, and n is an integer of 1 or 2.

Pyrimidinyloxy(thio)quinoline derivative, and agri-horticultural

Disclosed herein is a method for the stabilizing treatment of a catalyst comprising washing the catalyst with hot washing water following the preparation of the catalyst, the catalyst being composed principally of chromium oxide and used in the production of chlorine by the oxidation of hydrogen chloride with an oxygen-containing gas, thereby improving its catalytic activity and prolonging its life.

Method for stabilizing treatment of catalytic activity

The catalytic activity of a chromium oxide-based catalyst used in the production of chlorine by oxidation of hydrogen chloride gas with an oxygen-containing gas is regenerated by impregnating it with an aqueous solution of chromic acid anhydride or of a chromium salt and then calcining the catalyst at a temperature not higher than 800.degree. C.

Chromium oxide catalyst impregnation regeneration method

Bis(3-nitrophenoxy) derivatives of aromatic or bridged aromatic hydrocarbons are derived from m-dinitrobenzene and dihydroxy derivatives of said hydrocarbons and certain substituted derivatives thereof by a condensation reaction in dipolar aprotic solvents in the presence of bases. The bis(3-nitrophenoxy) derivatives and derivatives obtained are successively reduced to afford bis-(3-aminophenoxy)derivatives. This is a new method for reacting the dihydroxy-derivatives with m-dinitrobenzene, and hence can prepare novel bis(3-aminophenoxy) derivatives such as 4,4'-bis(3-amino-phenoxy)biphenyl, 1-[4-(3-aminophenoxy)phenyl]-1,3,3-trimethyl-6-(3-aminophenoxy)indan, 6,6'-bis(3-aminophenoxy)3,3,3',3'-tetramethyl-1,1'spirobiindan, and methyl substituted 2,2'-bis[4-(3-aminophenoxy)phenyl]propane.

Bis(3-aminophenoxy) aromatics and method of preparing the same

Aromatic bismaleimide derivatives and process for preparing same

Noval diamines, 2,6-bis(3-aminophenoxy)pyridine and 2,6-bis-(4-aminophenoxy)pyridine, are provided and the method of their preparation is disclosed. These diamines are useful as raw materials for polyimide. These diamines can be prepared by the reaction of 2,6-dichloropyridine or 2,6-dibromopyridine with 3-aminophenol or 4-aminophenol in aprotic polar solvents in the presence of bases. Besides, 2,6-bis(3-aminophenoxy)pyridine can also be prepared by the reaction of 2,6-dicholorpyridine or 2,6-dibromopyridine with 3-nitrophenol, followed by reducing resultant 2,6-bis(3-nitrophenoxy)pyridine.

2,6-bis(aminophenoxy)pyridine and method of preparing the same

1,3-Bis(3-aminophenoxy)-5-halogenobenzenes represented by the formula (I): ##STR1## wherein X is a chlorine or bromine atom, are novel compounds and can be prepared by reacting trihalogenobenzenes represented by the formula (II): ##STR2## wherein X.sub.1, X.sub.2 and X.sub.3 are each a chlorine or bromine atom, with 3-aminophenol in the presence of a dehydrohalogenating agent.

1,3-bis(3-aminophenoxy)-5-halogenobenzenes and process for their

A novel process for producing 6,6'-dihydroxy-3,3,3',3'-tetramethyl-1,1'-spirobiindane of the formula (1) ##STR1## which comprises heat-treating 2,2-bis(4-hydroxyphenyl)propane in the presence of a superacid-type resin or a perfluoroalkanesulfonic acid.

Process for producing

A process for producing 1,3-bis(3-aminophenoxy)-benzenes which are very useful as a monomer for heat-resistant high molecular weight polymers is provided, which process comprises dehalogenating a bis(3-aminophenoxy)-halogenobenzene by its reduction, which compound is selected from the group consisting of 1,3-bis(3-aminophenoxy)-5-halogenobenzenes, 1,3-bis(3-aminophenoxy)-2,4-dihalogenobenzenes and 1,5-bis(3-aminophenoxy)-2,4-dihalogenobenzenes, these raw material compounds being respectively obtained by reacting a 1,3,5-trihalogenobenzene, a 1,2,3,4-tetrahalogenobenzene or a 1,2,4,5-tetrahalogenobenzene with 3-aminophenol in the presence of a dehydrohalogenating agent.

Process for producing 1,3-bis(3-aminophenoxy)benzene

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Chiba-ken, Japan

Yukihiro Yoshikawa