Basf Aktiengesellschaft

Badische Anilin- & Soda-Fabrik Aktiengesellschaft

Other

Heinrich Adolphi

Karl Kiehs

Walter Seufert

Annegrit Baumann

Arno Lange

Hans-Peter Loeffler

Rainer Buerstinghaus

Hans Theobald

Rolf Huber

Wolfgang Seppelt

Juergen Varwig

Rainer Burstinghaus

Gerd-Ulrich Schwarz

Gerhard Hamprecht

Franz Merger

Bernd Zeeh

Karl-Heinz Koenig

Gerd Husslein

Karl Eicken

Norbert Rieber

Peter Hofmeister

Friedrich Linhart

Heinrich Boehm

Norbert Goetz

Helmut Hagen

Wolfgang Rohr

Ulrich Schirmer

Hardo Siegel

Volker Harries

Walter Himmele

Matthias Schwarzmann

Hans-Juergen Neubauer

Gerd Wunsch

Rolf-Dieter Acker

Rudolf Kropp

Erhard Henkes

Heinz-Guenter Oeser

Volker Kiener

Helmut Fleig

Walter Boell

Peter Hettinger

Hans Urbach

Hans J Schrepfer

Anna Steimmig

Hans-Dieter Hoffmann

Gerhard Bachmann

Horst Kummer

Albrecht Zschocke

Peter Heinze

Karl Keihs

N-benzoyl-N'-phenoxyphenylureas of the formula (I) ##STR1## where R.sup.1 is fluorine, chlorine or methyl, R.sup.2 is fluorine, chlorine or hydrogen, R.sup.3 and R.sup.4 are each chlorine or bromine and R.sup.5 and R.sup.6 can be identical or different and are each fluorine, chlorine, bromine, trifluoromethyl or hydrogen, processes for their preparation and their use for controlling pests.

N-benzoyl-N'-phenoxyphenylureas, their preparation and their use for

Bisthiolphosphates of the formula ##STR1## where R is alkyl, and pesticides containing these compounds.

Bisthiolphosphate, their use for combatting pests

Cinnamates of the formula I ##STR1## where R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 have the meanings stated in the description, processes for their preparation, and their use for pest control.

Propargyl cinnamates, their preparation and their use for controlling

Oximinophosphoric acid derivatives of the formula ##STR1## where R.sup.1 is a straight-chain or branched alkyl of not more than 4 carbon atoms, R.sup.2 is a straight-chain or branched alkoxy or alkylthio group of not more than 4 carbon atoms, straight-chain or branched alkyl of not more than 3 carbon atoms, phenyl, amino or a straight-chain or branched alkylamino or dialkylamino radical, where alkyl in each case is of not more than 4 carbon atoms, and X is oxygen or sulfur, a process for the manufacture of these oximinophosphoric acid derivatives, and their use for controlling pests.

Oximinophosphoric acid derivatives, and their use for controlling pests

Benzylbisthiophosphates of the formula ##STR1## where R is straight-chain or branched alkyl of 3 to 5 carbon atoms, their manufacture, and their use as pesticides.

Bisthiophosphates and their use for controlling pests

N-Benzoyl-N'-phenylureas of the formula ##STR1## where X, Y, Z and R have the meanings given in the description, are used for insect control.

N-benzoyl-N'-phenylureas and their use for insect control

Oximinophosphoric acid derivatives of the formula ##STR1## where R.sup.1 is straight-chain or branched alkyl of not more than 4 carbon atoms, R.sup.2 is a straight-chain or branched alkoxy or alkylthio group of not more than 4 carbon atoms, straight-chain or branched alkyl or not more than 3 carbon atoms, phenyl, amino or a straight-chain alkylamino or dialkylamino radical where alkyl in each case is of not more than 4 carbon atoms, R.sup.3 is methyl or ethyl and X is oxygen or sulfur, a process for the manufacture of these oximinophosphoric acid derivatives of the formula I, and their use as pesticides.

Oximinophosphoric acid derivatives and their use for controlling pests

Propargyl esters of the formula I ##STR1## where R.sup.1 is OC.sub.n H.sub.2n+1 (n=1 or 2), OCF.sub.3, OCF.sub.2 CHF.sub.2 or F and R.sup.2 is H, or R.sup.1 and R.sup.2 together form --O(CH.sub.2).sub.m O-- (m=1 or 2), a process for their preparation, and their use for controlling pests.

Novel esters, their preparation, and their use for controlling pests

Oximinophosphoric acid derivatives of the formula I ##STR1## where R.sup.1 is straight-chain or branched alkyl of not more than 4 carbon atoms,

Halovinylbenzyl esters of the formula I ##STR1## where R.sup.1 is ##STR2## R.sup.2 is H, CN, lower alkyl, lower alkenyl, lower alkynyl, lower haloalkyl or lower haloalkenyl, R.sup.3 is H, halogen or lower alkyl, R.sup.4 is H, lower alkyl, lower alkoxy or lower alkoxymethyl, R.sup.5 is lower alkyl, lower hal lk(en)yl or lower haloalkynyl, R.sup.6 and R.sup.7 are each lower alkyl or halogen, A is halogen, lower alkyl, lower alkoxy, lower haloalkyl, lower haloalkoxy, CN or NO.sub.2, m is 0 to 4, n is 1 to 3, B is lower alkyl, lower alkenyl, lower alkynyl or cycloalkyl, and X is H, halogen, lower haloalkyl, lower thioalkyl, lower alkoxy or lower alkyl, and halogen can be fluorine, chlorine or bromine and, in the case of R.sup.2, may furthermore be iodine, a process for their manufacture, and their use as pesticides.

Halovinylbenzyl esters and their use for controlling pests

O,S-dialkyl S-[carbamyloxyalkyl] dithiophosphates of the general formula (I) ##STR1## where, independently of one another, R.sup.1 and R.sup.2 are each alkyl of not more than 4 carbon atoms and R.sup.3, R.sup.4 and R.sup.5 are each hydrogen or alkyl of not more than 6 carbon atoms, or R.sup.4 and R.sup.5, together with the nitrogen atom to which they are bonded, form a saturated or olefinically unsaturated ring which contains not more than 6 carbon atoms and may or may not contain one or more oxygen, sulfur or nitrogen atoms, are used for controlling insects or mites.

O,S-dialkyl S-[carbamyloxyalkyl] dithiophosphates and their use as

Phosphates of the formula ##STR1## where R.sup.1 is alkyl of not more than 3 carbon atoms, R.sup.2 is alkoxy, alkylthio or alkylamino each of which has a straight-chain or branched alkyl substituent of not more than 5 carbon atoms, Y.sup.1 and Y.sup.2 independently of one another are each hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or halogen, and X is O or S, a process for their manufacture, and their use as insecticides and acaricides.

2-(substituted phenyl)-3-chloro-2-butene thio phosphates as insecticides

Dihalovinylphenyl phosphates of the formula I ##STR1## where A and B are each halogen or trihaloalkyl, X is oxygen or sulfur, Y and Z are each oxygen, sulfur or --NH--, R.sup.1 is alkyl, R.sup.2 is alkyl, haloalkyl, alkoxyalkyl or alkylthioalkyl, and R.sup.3, R.sup.4 and R.sup.5 independently of one another are each hydrogen, halogen, nitro, alkyl, cyano, alkoxy, alkoxyalkoxy, alkylthioalkylthio, alkoxyalkyl, alkylthioalkyl, alkylthio, trihaloalkyl or trihaloalkoxy, and pesticides containing these compounds.

Dihalovinylphenyl phosphates and their use as pesticides

2-Fluorophenyl(di)thiophosphates of the formula ##STR1## where R.sup.1 is alkyl of 1 to 3 carbon atoms, R.sup.2 is alkyl or haloalkyl of 1 to 5 carbon atoms, alkoxyalkyl or alkylthioalkyl of 2 to 6 carbon atoms or cycloalkyl of 3 to 6 carbon atoms, R.sup.3, R.sup.4 and R.sup.5 independently of one another are hydrogen, halogen, cyano, nitro or alkyl, alkoxy or alkylthio of 1 to 4 carbon atoms and X is oxygen or sulfur, and their use in pest control.

2-Fluorophenyl(di)thiophosphates and their use in pest control

Growing community of inventors

Limburgerhof, Germany

Heinrich Adolphi