TH80939A - Combination of agile compounds with insecticidal and tick-killing properties. - Google Patents

Abstract

DC60 (25/05/44) The combination of a novel active compound of fixed loop ketone and the active (1) to (6) active compounds listed in this description have properties. In killing ticks and insects very good The combination of the new fixed-loop ketone active compounds and the active compounds (1) to (6) listed in this description have effective insecticidal and tick-mite properties. Very good

Claims (6)

1. Mixture for the control of dangerous animals. Which includes a mixture Of the compound formula (I) (chemical formula) (I) where X represents C1-C6 alkyl, halogen, C1-C6 alkoxy or C1-C3 - halogeno-alkyl. Y is denoted by hydrogen, C1-C6. Alkyl, halogen, C1-C6 alkoxy or C1-C3-halogenous-alkyl Z is represented by C1-C6 alkyl, halogen, C1-C6 alkyl. The cox n is represented by a number from 0 to 3 A, represented by hydrogen, or in individual cases, C1-C12, a straight alkyl or branched chain with a halogen-substitution group, C3-C8 Alkyl, C3-C8 alkyl, C1-C10-alkyl, C1-C10-alkyl, C2-C8 alkyl, C1-C8-polyalcoxy-C2-C8-alkyl, C1-C10-Alkylthio - C2-C8-Alkyl or cycloalkyl with 3-8 atoms in the loop, which may be infused with oxygen. And / or sulfur, and may, in each case, be replaced with phenyl Or phenyl-C1-C6-alkyl with a group instead of halogen, C1-C6-alkyl, C1-C6-halogeno-alkyl, C1-C6-alkyl. C, C1-C6-halogeno-alkoxy, or nitro B denoted by hydrogen, C1-C6 alkyl or C1-C6 alkoxy-C2-C4-alkyl or by Where A and B are joined together with the carbon atoms where A and B are attached to form a ring of 3 to 8 saturated members. Or not saturated Which may be interpolated with oxygen and / or sulfur and may be replaced with halogen groups, C1-C6 alkyl, C1-C6 alkoxy, C1-C4-halogenos. Alkyls, C1-C4 - halogeno-alkoxies, C1-C4 - alkylthio, or may be substituted with phenyl or A and B may be fused together to form a bend. So G is represented by hydrogen (a) or represented by groups: (chemical formula) (b) (formula cm) (C) (chemical formula) (d) (chemical formula) (e) (chemical formula) (f) where R1 may Are represented in each case by C1-C20 - alkyl with halogen-substituting group, C2-C20 - alkyl, C1-C8-alkoxy-C2-C8-alkyl, C1. -C8 - Alkyl Thio -C2-C8-Alkyl, - C1-C8-Polyalcox C-C2-C8 - Alkyl or cycloalkyl with atoms. In a loop of 3-8 atoms where oxygen and / or sulfur atoms may be interpolated. May be substituted with phenyl group instead of halogen, nitro, C1-C6-alkyl, C1-C6-alkoxy, C1-C6. - HalogenOalkyl or C1-C6-HalogenOalcoxie May be substituted with phenyl-C1-C6-alkyl group instead of halogen, C1-C6-alkyl, C1-C6 alkoxy, C1-C6-halogenos. Alkyl or C1-C6-halogeno-alkoxie May choose to be substituted for each case with pyridyl, pyridyl, thiaasoyl or pyrazoid containing The halogen-substituted group and / or C1-C6-alkyl may be substituted in each case with pyridyl, pyrimidyl, thiazoyl. Or pyrazoil that contains A halogen-substituted group and / or C1-C6 alkyl may be selected with a phenoxy-C1-C6-alkyl with a halogen-substituted group and / or C1-C6-Al. The R2 kill may be substituted for each case with C1-C20 - alkyl with halogen substitution group, C2-C20 - alkyl, C1-C8-Alkoxy-C2-C8-Al. Kyl or C1-C8-polyalcoxy-C2-C8-alkyl may be substituted in each case with phenyl. Or benzyl with a group instead of halogen, nitrile, C1-C6-alkyl, C1-C6-alkoxy, or C1-C6-halogeno-alkyl, R3 may be chosen. Instead of C1-C8-alkyl with halogen substitution group, may be substituted in each case with phenyl or benzyl with a group instead of C1-C4-alkyl, halogen, C1-C4-halogenous, C1-C4-alkyl, C1-C4-halogenous, nitou R, or Cyano R4 and R5 are independent of each other. Which may be chosen instead in each case as well C1-C8-alkyl with halogen displacement group, C1-C8-alkyl, C1-C8-alkyl amino, di- (C1-C8)-alkyla. Mino, C1-C8-alkylthio, C2-C5-alkylthio, C2-C5-alkylthio or C3-C7-Cycloalkylthio May be substituted for each case with phenyl, phenoxy Or phenylthio with a group instead of Halogen, Nitrile, Cyano, C1-C4-Alcoxy, C1-C4-HalogenOalcocyte, C1-C4-Alkylthio, C1-C4-Halo The geno-alkyl-alkyl, C1-C4-alkyl or C1-C4-halogeno-alkyl R6 and R7 are independent of each other. Which may be substituted for each case with C1-C10 - alkyl with a replacement group Halogen, C1-C10-alkyl, C3-C8-alkyl or C1-C8-alkyl-C1-C8-alkyl, may be optional. Instead of phenyl with a group instead of a halogen, C1-C6-halogenoalkyl, C1-C6-alkyl or C1-C6-alkyl, may be substituted with Ben. Sil with a group instead of a halogen, C1-C6-alkyl, C1-C6-halogenous alkyl or C1-C6-alkyl. Or it may be merged into a band of 5 or 6 atoms, which may be interpolated with oxygen or sulfur atoms, and may be chosen as a C1-C6 alkyl replacement and with the following compounds. At least one of these is amitresbuprophosin, pimitrosin, pyriprotoxifentriazamate, IKI 200. 2. Mixture according to claim 1, consisting of compounds according to formula (I), where X represents C1-C4-alkyl, halogen, C1-C4-alkoxy or C1-C2 -. The halogenous Y is represented by hydrogen, C1-C4-alkyl, halogen, C1-C4-alkyl, or C1-C2-halogen.Z is represented by C1. -C4-alkyl, -halogen or C1-C4-alkoxy, n denoted by 0 or 1 A and B are joined together with the carbon atoms where A and B are attached to each other in the form. Band type A saturated form with 5 or 6 members with a group instead of C1-C4-alkyl or C1-C4-alkyl, G is represented by hydrogen (a), or may be represented by the following groups (chemical formula) ( b) (Chemical formula) (c) where R1 may be substituted for each case, C1-C16 - alkyl with halogen substitution group, C2-C16 - alkyl, C1-C6-Al. C-C2-C6-alkyl, or cycloalkyl with atoms in the loop 3-7 atoms, which may be interpolated with oxygen atoms. And / or 1 or 2 sulfur atoms may be substituted with phenyl groups instead of halogen, nitro, C1-C4 - alkyl, C1-C4 - alkoxy, C1-C3 -. The halogenous alkyl or C1-C3-halogenous alkyl, R2 may be substituted in each case by C1-C16 - alkyl with a halogen substitution group, C2-C16 -. Alkyl, or C1-C6-alkoxy-C2-C6-alkyl May be substituted in each case with phenyl Or benzyl with a group instead of halogen, nitrite, C1-C4-alkyl, C1-C4-alkyl, or C1-C4-halogeno-alkyl. 3. Mixture according to claim 1, which consists of a compound according to the formula (I-b-I) (chemical formula) (I-b-I). 4. Use of mixtures as defined in any one of Claims 1,2 and 3 for non-therapeutic hazardous animal control. 5. Non-therapeutic hazardous animal control methods are described in the sense that the mixtures are defined in one of Claims 1,2 and 3. Will cause dangerous animal reactions and / or their habitats 6. Process for preparing mixtures for insecticides And kill the tick mites Describe Characteristic in the sense that the mixture is defined in any of the 1,2 and 3 Claims. Mixed with Plates to expand, expand and / or surfactants.