Abstract: The invention relates to novel substituted phenyluraciles of the general formula (I) in which m, n, Q and R1-7 are each as defined in the description, and to processes for their preparation and to their use as herbicides.

Abstract: The invention relates to insecticidal mixtures of fipronil and agonists or antagonists of nicotinic acetylcholine receptors for the protection of industrial materials and plants.

Abstract: The present invention relates to a process for the preparation of compounds of the formula (I) by reacting compounds of the formula (II) in which Het, R1, R2 and R4 are as defined in the description, with anhydrous hydrogen chloride or compounds which generate hydrogen chloride.

Abstract: The invention relates to novel substituted 3-aryl-pyrazoles of the general formula (I) in which n, Q, R1, R2, R3, R4, R5 and X are each as defined in the description, and also to processes for their preparation and to their use as herbicides.

Abstract: The present invention provides a composition for inhibiting phase separation and the resulting non-uniform distribution of an active ingredient in low viscosity, water-based pesticide suspensions. In accordance with this invention, the composition comprises from about 0.003% to about 50% by weight of a pesticide, from about 0.5% to about 10% by weight of a wetting agent; from about 0.0% to about 0.8% by weight of a thickener; from about 0.1% to about 0.5% of an antimicrobial agent; from about 5% to about 20% of an anti-freeze; from about 1% to about 8% of a hydrophobic fumed silica; and from about 40% to about 95% of water. In an embodiment of the invention, the hydrophobic fumed silica results from a hydrophilic silica which is treated with dimethyldichlorosilane.

Abstract: The present invention relates to novel compounds of the formula (I) in which Het represents one of the groups  in which A, B, D, G, V, W, X, Y and Z are as defined in the description, processes and intermediates for their preparation, and to their use as pesticides and herbicides.

Abstract: A process for preparing a triazolinone includes the step of reacting a triazolinethione with an oxidant at a temperature range of from about 60° C. to about 100° C. in the presence of a base.

Abstract: Methods of purifying 2-methylthio-5-trifluoromethyl-1,3,4-thiadiazole include the steps of providing a first 2-methylthio-5-trifluoromethyl-1,3,4-thiadiazole composition comprising 2-methylthio-5-trifluoromethyl-1,3,4-thiadiazole and organic solvent; performing a first extraction of the 2-methylthio-5-trifluoromethyl-1,3,4-thiadiazole composition with a first inorganic acid solution; and performing a second extraction of the 2-methylthio-5-trifluoromethyl-1,3,4-thiadiazole composition with a second inorganic acid solution.

Abstract: Sulphonylbenzazolones of the formula in which R1, R2, R3, R4, R5 and Q are each as defined in the description, a process for preparing these compounds and their use as microbicides in crop protection and in the protection of materials.

Abstract: The present invention relates to a novel process for preparing benzofurandioneoxime derivatives by reacting benzofurandioneoxime derivatives with acids.

Abstract: The present invention relates to novel arylphenyl-substituted cyclic ketonols of the formula (I) in which X represents halogen, alkyl, alkoxy, alkenyloxy, alkylthio, alkylsulphinyl, alkylsulphonyl, halogenoalkyl, halogenoalkoxy, halogenoalkenyloxy, nitro, cyano or in each case optionally substituted phenyl, phenoxy, phenylthio, phenylalkoxy or phenylalkylthio, Y represents in each case optionally substituted cycloalkyl, aryl or hetaryl, W and Y independently of one another each represent hydrogen, halogen, alkyl, alkoxy, alkenyloxy, halogenoalkyl, halogenoalkoxy, halogenoalkenyloxy, nitro or cyano, CKE represents one of the groups in which A, B, D, G and Q1 to Q6 are each as defined in the description, to a plurality of processes for their preparation and to their use as pesticides and herbicides.

Abstract: The present invention relates to novel phenyl-substituted cyclic enaminones of the formula (I): in which Ar, X, Z, Y, K, n and m are each as defined in the description, to a plurality of processes and intermediates for their preparation and to their use as herbicides and pesticides.

Abstract: The present invention relates to novel arylphenyl-substituted cyclic ketoenols, their preparation and the use of such ketoenols as pesticides and/or herbicides. The novel arylphenyl-substituted cyclic ketoenols are of the formula (I) in which CKE refers to the cyclic ketoenol and W, X, Y and Z are as defined in the specification.

Abstract: The invention relates to novel substituted aryluracils of the formula (I): to processes for their preparation and to their use as crop protection agents.

Abstract: The invention relates to novel active substance combinations of valinamide derivatives of formula (I), wherein R1 and R2 have the meaning cited in the description, and fenamidone. The invention also relates to the use of novel active substance combinations to combat phytopathogenic fungi.

Abstract: The invention relates to novel glyoxylic acid amides, to a plurality of processes for their preparation and to their use for controlliing pests.

Abstract: The invention relates to a process for preparing substituted arylpyrazoles of the general formula (I) in which R1, R2, R3 and R4 are each as defined in the description, and to novel intermediates for preparing these arylpyrazoles.

Abstract: The invention relates to novel substituted phenyluracils of the general formula (I) in which the radicals n, Q, R1 to R6 are each as defined in the description, and to processes for this preparation and to their use as herbicides.

Abstract: The present invention is directed to compounds of having the formula (I) in which G represents a single bond or a grouping  and Z represents alkyl or halogenoalkyl or cycloalkyl or cycloalkylalkyl or heterocyclyl or heterocyclylalkyl or aryl or arylalkyl and L1, L2, L3 and L4 are identical or different and independently of one another in each case represent hydrogen, halogen, cyano, nitro or in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl or alkylsulphonyl having in each case 1 to 6 carbon atoms and in each case optionally substituted by 1 to 5 halogen atoms. The invention also relates to the preparation of such compounds and the use of such compounds to combat plant fungi and plant bacteria.

Abstract: The present invention relates to novel arylphenyl-substituted cyclic ketoenols of the formula (I) in which X represents halogen, alkyl, alkoxy, alkenyloxy, alkylthio, alkylsulphinyl, alkylsulphonyl, halogenoalkyl, halogeno-alkoxy, halogenoalkenyloxy, nitro, cyano or in each case optionally substituted phenyl, phenoxy, phenylthio, phenyl-alkoxy or phenylalkylthio, Y represents in each case optionally substituted cycloalkyl, aryl or hetaryl, Z represents hydrogen, halogen, alkyl, alkoxy, alkenyloxy, halogenoalkyl, halogenoalkoxy, halogenoalkenyloxy, nitro or cyano, CKE represents one of the groups  in which A, B, D, G and Q1 to Q6 are each as defined in the description, to a plurality of processes for their use as pesticides and herbicides.