Abstract:
Pesticidal mixtures comprising, as active components, 1 ) an anthranilamid compound of the formula I ,2 (I) Y wherein B1 is halogen, alkyl, haloalkyl, or haloalkoxy; B2 is halogen, haloalkyl, alkoxy, haloalkoxy, alkenyloxy, alkynyloxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, alkyl- S(=O)?-O- or haloalkyl S(O)x-O-, wherein x is 1 or 2 and the alkoxy radical may be substituted; R is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, wherein these groups are optionally substituted; X is halogen; Y is H or halogen; or the enantiomers or salts or N-oxides thereof, and 2) one or more compounds Il selected from group A consisting of organo(thio)- phosphates, carbamates, pyrethroids, growth regulators, nicotinic receptor agonists/antagonists compounds, GABA antagonist compounds, macrocyclic lactone insecticides, METI I acaricides, METI Il and III compounds, uncoupler compounds, oxidative phosphorylation inhibitor compounds, mixed function oxidase inhibitor compounds, sodium channel blocker compounds and others, all as defined in the description, in synergistically effective amounts, use of these mixture for combating insects, arachnids or nematodes in and on plants and for the protection of seeds, and for treating, controlling, preventing or protecting a warm-blooded animal or a fish against infestation or infection by parasites.
Abstract:
Use of compounds of formula (I) wherein Q is (II), (III), or (IV) ; X is chlorine, bromine, or fluorine; R , R are each independently H, alkyl, alkenyl, alkynyl, or cycloalkyl, alkylamino, dialkylamino, alkylcarbonylamino, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, or R and R may be taken together to form a ring represented by the structure (V); p,m are 1, 2 or 3; X' is oxygen, sulfur, amino, alkylamino, phenylamino, or methylene; Z is alkyl or phenyl; R is H, alkyl, alkenyl, alkynyl, cycloalkyl, wherein the carbon atoms in these groups may be substituted; R, R are H or alkyl, alkoxycarbonyl, alkylaminocarbonyl, or dialkylaminocarbonyl, wherein the carbon atoms in the these groups may be substituted; A is C-R or N; B is C-R or N; W is C-R or N; with the proviso that one of A, B and W is other than N; R , R , R are H, halogen, nitro, cyano, amino, mercapto, hydroxy, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, a 5- to 6-membered aromatic ringsystem which may contain 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen and which may be substituted; Y is hydrogen, halogen, cyano, nitro, amino, hydroxy, mercapto, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted; n is 0, 1, or 2; for combating parasites in and on animals.
Abstract translation:其中Q为(II),(III)或(IV)的式(I)化合物; X 1是氯,溴或氟; R 1,R 2各自独立地为H,烷基,烯基,炔基或环烷基,烷基氨基,二烷基氨基,烷基羰基氨基,烷基磺酰基或烷基亚磺酰基,其中这些基团中的碳原子可以被取代,或R 1, 和R 2可以一起形成由结构(Ⅴ)表示的环; p,m为1,2或3; X'是氧,硫,氨基,烷基氨基,苯基氨基或亚甲基; Z是烷基或苯基; R 3是H,烷基,烯基,炔基,环烷基,其中这些基团中的碳原子可以被取代; R 4是H或烷基,烷氧基羰基,烷基氨基羰基或二烷基氨基羰基,其中这些基团中的碳原子可以被取代; A为C-R 5或N; B是C-R 6或N; W是C-R 7或N; 条件是A,B和W之一不是N; R 5,R 6,R 7是H,卤素,硝基,氰基,氨基,巯基,羟基,烷基,烯基,炔基,环烷基,烷氧基,烷基氨基,二烷基氨基,烷硫基,烷基磺酰基或烷基亚磺酰基, 其中这些基团中的碳原子可以被取代,可以含有1至4个选自氧,硫和氮并且可以被取代的杂原子的5至6元芳族环系统; Y是氢,卤素,氰基,硝基,氨基,羟基,巯基,烷基,烯基,炔基,环烷基,烷氧基,烷基氨基,二烷基氨基,烷硫基,烷基磺酰基或烷基亚磺酰基,其中这些基团中的碳原子可以被取代; n为0,1或2; 用于对抗动物体内及其上的寄生虫。
Abstract:
1.- El uso de los compuestos de fórmula I en la cualX1 es cloro, bromo o flúor;R1, R2 son individual e independientemente hidrógeno, alquilo-C1-C10, alquenilo-C3-C10, alquinilo-C3-C10, o cicloalquilo-C3-C12, alquilamino-C1-C6, di(alquil-C1-C6)-amino, alquilcarbonilamino-C1-C6, alquilsulfonilo-C1-C6, o alquilsulfinilo-C1-C6, en donde los átomos de carbono en estos grupos pueden estar substituidos con;1 a 3 halógeno, hidroxy, nitro, ciano, amino, mercapto, alcoxi-C1-C6, haloalcoxi-C1-C6, alquiltio-C1-C6, haloalquiltio-C1-C6, alquilsulfonilo-C1-C6, alquilsulfinilo-C1-C6, haloalquilsulfonilo-C1-C6, haloalquilsulfinilo-C1-C6, o cicloalquilo-C3-C6 el cual puede estar substituido con 1 a 3 grupos R# , oR# es halógeno, ciano, nitro, hidroxi, mercapto, amino, alcoxi-C1-C6, alqueniloxi-C2-C6, alquiniloxi-C2-C6, haloalcoxi-C1-C6, alquiltio-C1-C6, o haloalquiltio-C1-C6, alquilsulfonilo-C1-C6, alquilsulfinilo-C1-C6, alquilamino-C1-C6, di(alquil-C1-C6)-amino, alquilcarbonilo-C1-C6, alcoxicarboniloC1-C6, o di-alquil(C1-C6)aminocarbonilo;formilo, alquilcarbonilo-C1-C6, C(=O)NRaRb, CO2RC, Rd, Re, fenilo el cual puede estar substituido con 1 a 3 grupos R#, o piridilo el cual puede estar substituido con 1 a 3 grupos R#, Ra, Rb, RC son individual e independientemente hidrógeno o alquilo-C1-C4 el cual puede estar substituido con 1 o 3 grupos R#;Rd es NRiRj oRi, Rj son individual e independientemente hidrógeno o alquilo-C1-C4 el cual puede estar substituido con 1 a 3 grupos R#;p, m son individual e independientemente 0, 1, 2, o 3, con la condición de que p y m ambos no sean 0;X es oxígeno, azufre, amino, alquilamino-C1-C4, o fenilamino, o, si p es 0 entonces X también puede ser ...
Abstract:
Utilisation de dérivés N-arylhydrazine pour la lutte contre des nuisibles dans et sur des animaux Utilisation de composés de formule I dans laquelle Q est X1 est un atome de chlore, un atome de brome, ou un atome de fluor ; R1, R2 sont chacun indépendamment un atome d'hydrogène, un groupe alkyle, un groupe alcényle, un groupe alcynyle, ou un groupe cycloalkyle, un groupe alkylamino, un groupe dialkylamino, un groupe alkylcarbonylamino, un groupe alkylsulfonyle, or un groupe alkylsulfinyle, où les atomes de carbone dans ces groupes peuvent être substitués, ou R1 et R2 peuvent être pris conjointement pour former un noyau représenté par la structure p, m valent 1, 2 or 3 ; X' est un atome d'oxygène, un atome de soufre, un groupe amino, un groupe alkylamino, un groupe phénylamino, or un groupe méthylène ; Z est un groupe alkyle ou un groupe phényle ; R3 est un atome d'hydrogène, un groupe alkyle, un groupe alcényle, un groupe alcynyle, un groupe cycloalkyle, où les atomes de carbone dans ces groupes peuvent être substitués ; R, R4 sont un atome d'hydrogène ou un groupe alkyle, un groupe alkoxycarbonyle, un groupe alkylaminocarbonyle, ou un groupe dialkylaminocarbonyle où les atomes de carbone dans ces groupes peuvent être substitués ; A est un groupe C-R5 ou un atome d'azote ; B est un groupe C-R6 ou un atome d'azote ; W est un groupe C-R7 or un atome d'azote ; à condition que l'un parmi A, B et W soit autre qu'un atome d'azote ; R5, R6, R7 sont un atome d'hydrogène, un atome d'halogène, un groupe nitro, un groupe cyano, un groupe amino, un groupe mercapto, un groupe hydroxy, un groupe alkyle, un groupe alcényle, un groupe alcynyle, un groupe cycloalkyle, un groupe alcoxy, un groupe alkylamino, un groupe dialkylamino, un groupe alkylthio, un groupe alkylsulfonyle, ou un groupe alkylsulfinyle, où les atomes de carbone dans ces groupes peuvent être substitués, un système de noyau aromatique à 5-6 chaînons, qui peut renfermer de 1 to 4 hétéroatomes choisis parmi un atome d'oxygène, un atome de soufre et un atome d'azote, et qui peut être substitué ; Y est un atome d'hydrogène, un atome d'halogène, un groupe cyano, un groupe nitro, un groupe amino, un groupe hydroxy, un groupe mercapto, un groupe alkyle, un groupe alcényle, un groupe alcynyle, un groupe cycloalkyle, un groupe alcoxy, un groupe alkylamino, un groupe dialkylamino, un groupe alkylthio, un groupe alkylsulfonyle, ou un groupe alkylsulfinyle, où les atomes de carbone dans ces groupes peuvent être substitués : n vaut 0, 1, ou 2 ; pour la lutte contre des parasites dans et sur des animaux.
Abstract:
Use of compounds of formula I wherein Q is X 1 is chlorine, bromine, or fluorine; R 1 , R 2 are each independently H, alkyl, alkenyl, alkynyl, or cycloalkyl, alkylamino, dialkylamino, alkylcarbonylamino, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, or R 1 and R 2 may be taken together to form a ring represented by the structure p, m are 1, 2 or 3; X' is oxygen, sulfur, amino, alkylamino, phenylamino, or methylene; Z is alkyl or phenyl; R 3 is H, alkyl, alkenyl, alkynyl, cycloalkyl, wherein the carbon atoms in these groups may be substituted; R, R 4 are H or alkyl, alkoxycarbonyl, alkylaminocarbonyl, or dialkylaminocarbonyl, wherein the carbon atoms in the these groups may be substituted; A is C-R 5 or N; B is C-R 6 or N; W is C-R 7 or N; with the proviso that one of A, B and W is other than N; R 5 , R 6 , R 7 are H, halogen, nitro, cyano, amino, mercapto, hydroxy, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, a 5 to 6-membered aromatic ringsystem which may contain 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen and which may be substituted; Y is hydrogen, halogen, cyano, nitro, amino, hydroxy, mercapto, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted; n is 0, 1, or 2; for combating parasites in and on animals.
Abstract:
Use of compounds of formula I wherein Q is X 1 is chlorine, bromine, or fluorine; R 1 , R 2 are each independently H, alkyl, alkenyl, alkynyl, or cycloalkyl, alkylamino, dialkylamino, alkylcarbonylamino, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, or R 1 and R 2 may be taken together to form a ring represented by the structure p, m are 1, 2 or 3; X' is oxygen, sulfur, amino, alkylamino, phenylamino, or methylene; Z is alkyl or phenyl; R 3 is H, alkyl, alkenyl, alkynyl, cycloalkyl, wherein the carbon atoms in these groups may be substituted; R, R 4 are H or alkyl, alkoxycarbonyl, alkylaminocarbonyl, or dialkylaminocarbonyl, wherein the carbon atoms in the these groups may be substituted; A is C-R 5 or N; B is C-R 6 or N; W is C-R 7 or N; with the proviso that one of A, B and W is other than N; R 5 , R 6 , R 7 are H, halogen, nitro, cyano, amino, mercapto, hydroxy, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, a 5 to 6-membered aromatic ringsystem which may contain 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen and which may be substituted; Y is hydrogen, halogen, cyano, nitro, amino, hydroxy, mercapto, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted; n is 0, 1, or 2; for combating parasites in and on animals.
Abstract:
El uso de los compuestos de fórmula I en la cual Q es X1 es cloro, bromo o flúor;R1, R2 son individual e independientemente H, alquilo, alquenilo, alquinilo o cicloalquilo, alquilamino, dialquilamino, alquilcarbonilamino, alquilsulfonilo o alquilsulfinilo, en donde los átomos de carbono en estos grupos pueden estar substituidos, o R1 y R2 pueden ser tomados en forma conjunta para formar un anillo representado por la estructura ;p, m son 1, 2 o 3; X' es oxígeno, azufre, amino, alquilamino, fenilamino, ometileno; Z es alquilo o fenilo;R3 es H, alquilo, alquenilo, alquinilo, cicloalquilo, en donde los átomos de carbono en estos grupos puede estar substituidos; R, R4 son H o alquilo, alcoxicarbonilo, alquilaminocarbonilo, o dialquilaminocarbonilo, en donde los átomos de carbono en estos grupos pueden estar substituidos;A es C-R5 o N; B es C-R6 o N; W es C-R7 o N; con la condición de que uno de A, B y W sea diferente a N; R5, R6, R7 son H, halógeno, nitro, ciano, amino, mercapto, hidroxi, alquilo, alquenilo, alquinilo, cicloalquilo, alcoxi, alquilamino, dialquilamino, alquiltio, alquilsulfonilo, o alquilsulfinilo, en donde los átomos de carbono en estos grupos pueden estar substituidos, un sistema de anillos aromáticos de 5 a 6 miembros el cual puede contener de 1 a 4 heteroátomos seleccionados entre oxígeno, azufre y nitrógeno y el cual puede estar substituido;Y es hidrógeno, halógeno, ciano, nitro, amino, hidroxi, mercapto, alquilo, alquenilo, alquinilo, cicloalquilo, alcoxi, alquilamino, dialquilamino, alquiltio, alquilsulfonilo, o alquilsulfinilo, donde los átomos de carbono en estos grupos pueden estar sustituidos;n es 0, 1 o 2;para combatir parásitos en y sobre animales
Abstract:
Use of compounds of formula I wherein Q is X 1 is chlorine, bromine, or fluorine; R 1 , R 2 are each independently H, alkyl, alkenyl, alkynyl, or cycloalkyl, alkylamino, dialkylamino, alkylcarbonylamino, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, or R 1 and R 2 may be taken together to form a ring represented by the structure p, m are 1, 2 or 3; X' is oxygen, sulfur, amino, alkylamino, phenylamino, or methylene; Z is alkyl or phenyl; R 3 is H, alkyl, alkenyl, alkynyl, cycloalkyl, wherein the carbon atoms in these groups may be substituted; R, R 4 are H or alkyl, alkoxycarbonyl, alkylaminocarbonyl, or dialkylaminocarbonyl, wherein the carbon atoms in the these groups may be substituted; A is C-R 5 or N; B is C-R 6 or N; W is C-R 7 or N; with the proviso that one of A, B and W is other than N; R 5 , R 6 , R 7 are H, halogen, nitro, cyano, amino, mercapto, hydroxy, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, a 5 to 6-membered aromatic ringsystem which may contain 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen and which may be substituted; Y is hydrogen, halogen, cyano, nitro, amino, hydroxy, mercapto, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted; n is 0, 1, or 2; for combating parasites in and on animals.