Bayer Aktiengesellschaft

Nihon Bayer Agrochem, K.k.

Lanxess Deutschland Gmbh

Michael Schwamborn

Hans-Joachim Santel

Robert R Schmidt

Harry Strang

Peter Babczinski

Werner Daum

Klaus-Helmut Muller

Bernd Baasner

Gerd Hanssler

Erich Klauke

Ludwig Eue

Hermann Hagemann

Engelbert Kuhle

Klaus Sasse

Wilfried Paulus

Hans-Georg Schmitt

Peter Wachtler

Gerhard Heywang

Shinichi Tsuboi

Gunther Beck

Otto Exner

Shinzaburo Sone

Robert H Strang

Monika Frie

Georg-Wilhelm Ludwig

Toru Obinata

Wilhelm Brandes

Reiner Fischer

Albrecht Marhold

Klaus Lurssen

Wolfgang Behrenz

Martin Kugler

Andreas Krebs

Winfried Lunkenheimer

Torsten Groth

Ernst Kysela

Lutz Heuer

Karlfried Dickore

Hans-Ulrich Buschhaus

Josef Kasbauer

Klaus-Helmut M Uller

Bernd-Michael Konig

Carl Fedtke

Wilheim Brandes

There are described the use of &#x3b1;-(4-chlorophenyl)-&#x3b1;-(1-cyclopropylethyl)-1H-1,2,4-triazole-1-ethanol as a microbicide for the protection of industrial materials, and compositions containing this compound.

Microbicidal compositions

The use of the compounds of the formula (I)as agents for preserving technical materials against insects.

Agents for preserving technical materials against insects

The use of the compounds of the formula (I)

A process for the preparation of a N-)ortho-alkylphenyl)-imide of the formula ##STR1## in which R.sup.1 to R.sup.9 is defined in the specification which comprises reacting a cyclic anhydride of the formula ##STR2## wherein R.sup.6 to R.sup.9 are difined in the specification with an amine of the formula ##STR3## optionally in the presence of an acid catalyst and optionally in the presence of a solvent which is immiscible or only slightly miscible with water but can form an azeotrope with water, at a temperature between 100.degree. to 200.degree. C. under conditions so that the water formed during the reaction is removed from the reaction mixture without the addition of a polymerization inhibitor or a dipolar solvent. The final products are used as intermediates to prepare heat-stable plastics as well as intermediates to prepare pharmaceutical and agricultural chemicals.

Process for the preparation of N-(ortho-alkylphenyl)-imides

Herbicidal sulphonylaminocarbonyltriazolinones of the formula ##STR1## in which R.sup.1 represents hydrogen, hydroxyl or amino, or represents an optionally substituted radical from the series comprising alkyl, alkenyl, alkinyl, cycloalkyl, aralkyl, aryl, alkoxy, alkenyloxy, alkylamino and dialkylamino,

Sulphonylaminocarbonyltriazolinones

Herbicidal sulphonylaminocarbonyltriazolinones of the formula ##STR1## in which R.sup.1 represents hydrogen, hydroxyl or amino, or represents an optionally substituted radical from the series comprising alkyl, alkenyl, alkinyl, cycloalkyl aralkyl, aryl, alkoxy, alkenyloxy, alkylamino and dialkylamino,

The invention relates to the use of certain 1-[2-pyri(mi)dyl]-5-hydroxy-pyrazoles which are characterized by formula (I) given in the description, as microbicides for the protection of industrial materials, and to certain novel 1-[2-pyri(mi)dyl]-5-hydroxy-pyrazoles which are characterised by formula (II) given in the description.

1-[pyri(mi)dyl-(2)]-5-hydroxy-pyrazole microbicides

The invention relates to the use of certain 1-[2-pyri(mi)dyl]-5-hydroxy-pyrazoles which are characterized by formula (I) given in the description, as microbicides for the protection of industrial materials, and to certain novel 1-[2-pyri(mi)dyl]-5-hydroxy-pyrazoles which are characterized by formula (II) given in the description.

1-[pyri(mi)dyl-(2)]-hydroxy-pyrazole microbicides

Herbicidal sulphonylaminocarbonyltriazolinones of the formula ##STR1## in which R.sup.1 represents hydrogen, hydroxyl or amino, or represents an optionally substituted radical from the series comprising alkyl, alkenyl, akinyl, cycloalkyl, aralkyl, aryl, alkoxy, alkenyloxy, alkylamino and dialkylamino,

Herbicidal thiazolecarboxamide derivatives of the formula ##STR1## in which n represents the numbers 0 or 1,

Herbicidal thiazolecarboxamide derivatives

New fluorinated tertiary butylamines of the formula ##STR1## are prepared from halogenated pivalic acid halides by a reaction sequence which comprises preparing the fluorinated pivalic acid and decomposition of the azide to the corresponding isocyanate. The isocyanate can be converted to the fluorinated tertiary butylamine acid addition salt by acid hydrolysis or directly to the amine by treatment with base. In addition, the present amines can be prepared by reaction of a pivalic acid amide with hypochlorite. The new butylamines can be used in the preparation of benzoic acid amides having insecticidal action.

Fluorinated tertiary butylamines

The fungicidally active N-sulphenylated 2-amino-4-chloro-thiazole-sulphonamides of the formula ##STR1## wherein R.sup.1 and R.sup.2 independently of one another denote hydrogen, alkyl, alkenyl, alkinyl, cycloalkyl, aryl, aralkyl or an aromatic or a non-aromatic heterocyclic radical and

N-sulphenylated 2-amino-4-chloro-thiazole-sulphonamides, their use,

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Cologne, Germany

Michael Schwamborn