Abstract:
Substituted carbamoyl triazoles have the formula (I), in which the variables have the following meanings: R is hydrogen, C1-C6 alkyl, C1-C6 alkyl halide, C3-C8 cycloalkyl, C3-C6 alkenyl or C3-C6 alkinyl; R is R , C1-C6 alkoxy or C1-C6 alkoxy halide; or R and R form together an optionally substituted C2-C5 alcandiyl radical, and if they form a C4-C5 alcandiyl radical one CH2 group may be substituted by oxygen or a group NH or N-C1-C6 alkyl; R , R and R are hydrogen, cyano, C1-C6 alkyl, C1-C6 alkyl halide, C3-C6-cycloalkyl, C2-C6 alkenyl, C2-C6 alkinyl, C1-C6 alkoxy, C1-C6 alkoxy halide, C1-C6 alkylthio, C1-C6 alkyl carbonyl, C1-C6 alkyl halide carbonyl, C1-C6 alkoxycarbonyl, optionally substituted phenyl or benzyl; A is an optionally substituted, saturated or partially unsaturated heterocycle containing one to three heteroatoms selected from the group of oxygen, sulphur and nitrogen, and is five- or six-membered; n equals 0, 1 or 2, provided that A does not stand for 1,3-dioxolan-2-yl or 1,3-dioxan-2-yl. Also disclosed are salts of (I) useful in agriculture, a process for preparing the same and their use as herbicides.
Abstract:
The present invention relates to carboxylic acid derivatives of formula (I) in which the radicals have the meaning given in the description, and the production of these substances and their use as medicaments.
Abstract:
Aromatic sulphoxide and sulphone of formula (I) in which the substituents and the indices have the following meaning: Het is a five- or six-membered heterocycle from the group thiophene; furan, pyrrole, pyrazole, imidazole, oxazole, thiazole, isoxazole, isothiazole, 1,2,3 triazole, (1H)1,2,4 triazole, (4H)1,2,4 triazole, pyridine, pyridine N oxide, pyridazine, pyrimidine, pyrazine, 1,2,3 triazine, 1,3,5 triazine, 1,2,4 triazine; X is nitrogen or a C-H methine group; Y is oxygen or sulphur; Z is nitrogen or a C-R grouping; n is 1 or 2; and in which the substituents R, R , R , R and R have the meanings given in claim 1; a process for their preparation and their use as herbicide.
Abstract:
The invention relates to organic tin compounds of formula (I), wherein the rests have the following meaning: R is optionally substituted benzyl, alkyl, dihydropyranyl, trialkyl silyl, alkoxy alkyl and dialkoxy alkyl; and R is alkyl, cycloalkyl. It also relates to a process for preparing said compounds, a biocidal agent and their use as biocides.
Abstract:
1. Herbizide Mischung umfassend a) als Komponente A eine herbizid wirksame Menge eines Benzoylpyrazols der Formel (I), worin die Variablen folgende Bedeutungen haben: R 1 Halogen, C 1 -C 4 -Alkyl, C 1 -C 4 -Alkoxy; R 2 C 1 -C 4 -Alkyl, C 1 -C 4 -Halogenalkyl, C 1 -C 4 -Alkoxy; R 3 C 1 -C 4 -Alkylsulfonyl; R 4 Wasserstoff, C 3 -C 6 -Alkinyl, C 3 -C 6 -Halogenalkinyl; R 5 C 2 -C 4 -Alkyl, C 3 -C 4 -Cycloalkyl; R 6 Wasserstoff, C 1 -C 4 -Alkyl; oder dessen landwirtschaftlich geeigneten Salzes; und b) als Komponente B eine antidotisch wirksame Menge eines Safeners, und 2. Verbindungen der Formel I, worin die Variablen oben genannte Bedeutungen haben, ausgenommen R 4 ungleich Wasserstoff.
Abstract:
The present invention relates to azolin-2-ylamino compounds of formulae (I) and (II), wherein n is 0 to 3; Ar is phenyl; A is a radical of formulae A 1 or A 2 , wherein * indicates the point of attachment; X is S, O or N(R 10 ); R 7a-d are H, halogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkylamino or C 3 -C 6 -cycloalkyl; R 8-10 are H, CN, NO 2 , C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 8 -cycloalkyl, Ar 3 , -B-C(=O)R a , -B-C(=S)R a , -B-C(=NR f )R a , etc., wherein B is a single bond or C 1 -C 4 -alkanediyl; R 1 is H, halogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, phenyl or benzyl; R 2,3 are H, halogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, phenyl or benzyl; R 4 is H, halogen, CN, N 3 , NO 2 , C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 8 -cycloalkyl, a heterocycle, Ar 5 , -C(=O)R a, -C(=S)R a , -C(=NR f )R a , etc.; or R 4 and R 5 together form a carbocycle or heterocycle; R 5,6 are H, halogen, CN, N 3 , NO 2 , C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 8 -cycloalkyl, heterocycle, Ar 8 , -C(=O)R a , -C(=S)R a , -C(=NR f )R a , etc.; or R 5 and R 6 together form a carbocycle or heterocycle; R a-h are H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 8 -cycloalkyl, heterocycles or Ar 10 ; Ar 1 to 11 are phenyl, naphthyl or heteroaryl; and A' is a radical of formula A 3 , wherein W is halogen or OR 11 ; R 11 is H or -C(=O)-R i ; R i is H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C3-C8-cycloalkyl, heterocycle or Ar 12 ; and Ar 12 is phenyl, naphthyl or heteroaryl; as well as to agricultural composition containing such compounds, the use of such compounds for controlling animal pests, seed, comprising such compounds, a method for controlling animal pests and a method for treating or protecting an animal from infestation or infection by parasites.
Abstract:
The present invention relates to the use of 6-halogeno-[1,2,4]-triazolo[1,5-a]-pyrimidine compounds of the general formula (I) wherein A, R 1 , R 2 , R 3 and R 4 are as defined in the specification; and/or an enantiomer, diastereomer, tautomer, solvate, crystalline form or veterinarily acceptable salt thereof alone or in combination with an additional anti-parasiticidal agent for combating parasites in and on animals.
Abstract:
The present invention relates to the use of aminoazoline and urea derivatives for com- bating animal pests. The invention also relates to a method for controlling animal pests by using these compounds, to seed and to an agricultural and veterinary composition comprising said compounds and to specific azoline and urea derivatives.
Abstract:
The present invention relates to new azine compounds which are useful combating animal pests, in particular insects and nematodes and to the salts thereof. The invention also relates to a method for combating insects, nematodes and arachnids. The azine compounds of the invention are described by the general formula (I) wherein is absent or a covalent bond; n is 0 or 1, in paarticular 0; A is an optionally substituted cyclic radical selected from phenyl and a 5- or 6-membered heterocyclic radical with 1, 2, 3, or 4 heteroatoms; Ar is an optionally substituted aromatic radical selected from phenyl, pyridyl, pyrimidyl, furyl and thienyl, x is selected from halogen, OR 7 , SR 7 , SOR 7 ,SO 2 R 7 , C 1 -C 4 -alkyl and C 1 -C 4 -haloalkyl; and wherein R 1 to R 4 and R 7 are as described in the claims and the specification.
Abstract:
N-(4-Pyridyl)methylsulfonamides for combating arthropodal pests The present invention relates to the use of N-(4-pyridyl)methylsulfonamides of the formula for combating arthropodal pests (harmful arthropodes) and for protecting materials against infestation and/or destruction by said pests: (I) where the substituents are as follows: R 1 is hydrogen, C 1 -C 4 -alkyl, C 1- C 4 -alkoxy, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl or benzyl; R 2 , R 3 , R 4 , R 5 independently of one another are hydrogen, halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkoxy or C 1 -C 4 -haloalkyl; R 2 and R 3 or R 4 and R 5 together with the carbon atoms to which they are attached may also form a condensed 5- or 6-membered hydro- carbon ring, it being possible for the hydrocarbon ring to carry one or two groups R 2' , R 3' , R 2' , R 3' independently of one another are halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, halomethoxy or halomethyl; X is a cyclic radical selected from phenyl, naphthyl and five- or six-membered saturated, partially unsaturated or aromatic heterocycles, the heterocycle being attached to the sulfur atom via a carbon atom and containing 1 , 2 or 4 heteroatoms selected from the group consisting of O, N and S, where the cyclic radical X may carry 1 , 2, 3 or 4 substituents R a .