Abstract:
Disclosed are fungicidal mixtures containing a benzamidoxime of formula (I), wherein R can represent hydrogen, halogen, alkyl, alkyl halide, alkoxy, or haloalkoxy while n can represent 1, 2, or 3, and one component selected among benomyl, carbendazim, debacarb, fuberidiazole, thiabendazole, thiophanate-methyl, captan, folpet, fenamidone, famoxadone, maneb, mancozeb, thiram, and metalaxyl-M as active components at a synergistically effective quantity. Also disclosed are methods for controlling fungi, the use of the inventive compounds for producing such mixtures, and agents containing said mixtures.
Abstract:
Disclosed are fungicidal mixtures for controlling rice pathogens, containing a synergistically effective amount of 1) a compound of formula (I), and 2) a compound of formula (II) as active components, methods for controlling destructive fungi by means of mixtures of compound I and compound II, the use of compounds I and II for producing such mixtures, and agents containing said mixtures.
Abstract:
Substituted 6-(2-halogenphenyl)-triazolopyrimidines of formula (I) in which R1 denote alkyl, alkenyl, alkynyl, alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or a 5- or 6-membered saturated, unsaturated, or aromatic heterocycle, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, wherein R and R radicals may be substituted as defined in the description, R denote hydrogen, or a group mentioned for R ; or R and R together with the interjacent nitrogen atom represent a 5- or 6-membered heterocycle, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which ring may be substituted as defined in the description; Hal is halogen; L , L independently denote hydrogen, halogen, or alkyl; L is hydrogen, halogen, haloalkyl, or NH2, NHR , or N(Rb)2, wherein Rb is as defined in the description,wherein at least one from L , L , and L is not hydrogen; X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
Abstract translation:取代的式(I)的6-(2-卤代苯基) - 三唑并嘧啶,其中R1表示烷基,烯基,炔基,链二烯基,卤代烷基,卤代烯基,环烷基,苯基,萘基或5-或6-元饱和,不饱和或 芳族杂环,其含有1-4个氮原子或一至三个氮原子和一个硫或氧原子,其中R 1和R 2基团可以如说明书中所定义地被取代,R 2表示氢,或 R 1中提到的基团; 或R 1和R 2连同相邻的氮原子表示含有1-4个氮原子或1-3个氮原子和一个硫或氧原子的5-或6-元杂环,该环可以被取代 如说明书中所定义的; 卤素是卤素; L 1,L 3独立地表示氢,卤素或烷基; L 2是氢,卤素,卤代烷基或NH 2,NHR b或N(R b)2,其中R b如说明书中所定义,其中至少一个L 1,L 2, 而L 3不是氢; X是卤素,氰基,烷基,烷氧基,卤代烷氧基或烯氧基,它们的制备方法,含有它们的组合物和它们用于防治植物病原性真菌的用途。
Abstract:
The invention relates to agrochemical compositions with a fungicidal action, containing compounds of formula (I) as their active agents. The radicals of said formula have the following meanings: R means hydrogen, C1-C6-alkyl, C1-C6-alkylcarbonyl, formyl or C1-C6-halogenalkylcarbonyl; R means halogen, C1-C6-alkylthio, C1-C6-alkoxy, C3-C6-cycloalkyl-C1-C6-alkoxy, C1-C6-alkoxy-C1-C6-alkyl, halogen-C1-C6-alkoxy, C1-C6-alkylsulfonyl, C1-C6-alkylsulfinyl, halogen-C1-C6-alkylsulfonyl, cyano or a radical NR R ; R -R mean hydrogen, halogen, C1-C8-cycloalkyl, C1-C6-alkyl, halogen-C1-C6-alkyl, C1-C6-alkoxy, halogen-C1-C6-alkoxy, C1-C6-alkylsulfonyl, halogen-C1-C6-alkylsulfonyl, formyl, C1-C6-alkylcarbonyl, cyano, C1-C6-alkylthio or phenyl, which can optionally be substituted by halogen atoms, C1-C6-alkyl or halogen-C1-C6-alkyl groups; R means hydrogen, C1-C6-alkyl; and R means C1-C6-alkyl, C1-C8-cycloalkyl or together with R and the nitrogen atom to which they are bonded, a saturated or unsaturated heterocyclic five or six-membered ring which has one or two heteroatoms selected from a group consisting of nitrogen atoms and oxygen atoms. The invention also relates to salts of said compositions which are suitable for agricultural use.
Abstract:
The invention relates to novel cycloalkylalkane carboxylic acid amides of the general formula (I), as well as salts thereof which are suitable for use in agriculture, in which the substituents have the following meanings: A is C3-C6 cycloalkyl which can carry one or more substituents; Alk is straight-chain or branched C1-C6-alkylene; R is C1-C6-alkyl or C2-C6-alkenyl, which can carry one or more substituents; R , R are hydrogen, C1-C6-alkyl or C2-C6-alkenyl, which rests can be partly or fully halogenated; and W is a fused bicyclic ring system with six ring atoms each. The invention also relates to fungicidal agents containing a compound of formula (I) as plant protectant.
Abstract:
The invention relates to fungicidal mixtures containing in the form of active agents: a triazolopyrimidine derivative of formula (I) and thiophanate-methyl of formula (II) in synergistically active quantity and to a method for controlling harmful fungi by means of the mixture of the compounds I and II, thereby making it possible to produce said mixtures and the products containing them.
Abstract:
Fungicide mixtures contain as active components (1) the triazolopyrimidine derivative of formula I, and (2) iprodiones of formula II in a synergistically effective amount. Also disclosed are processes for combating harmful fungi with mixtures of compound I with compound II and the use of compound I with compound II for producing such mixtures, as well as agents which contain these mixtures.
Abstract:
Disclosed are fungicidal mixtures containing: 1) a triazolopyrimidine derivative of formula (I), and 2) metconazole of formula (II) at a synergistically effective quantity as active components, methods for controlling harmful fungi that belong to the class of oomycetes with the aid of mixtures of compound (I) and compound (II), the use of compound (I) and compound (II) for producing such mixtures, and agents containing said mixtures.
Abstract:
The invention relates to a fungicidal mixture that comprises (1) 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazolo-3-thion (prothioconazole) or the salts or adducts thereof and at least one further fungicidal composition, selected from (2) boscalid or (3) carboxine or (4) metrafenone or (5) a compound of formula (V) or (6) a compound of formula (VI) or (7) quinoxyfen or (8) dithianon or (9) thiram or (10) mepiquat chlorides or (11) cyazofamid or (12) fenoxanil or (13) a compound of formula (XIII) or (14) thiophanate methyl or (15) carbendazim or (16) metalaxyl or (17) fludioxonil or (18) thiabendazole or (19) quintozene or (20) prochloraz or (21) anthraquinone in a synergistically effective amount.
Abstract:
The invention relates to 7-(R) aminotriazolopyrimidines of formula (I), in which the substituents and index have the following definitions: R represents hydrogen or methyl; R represents methyl; R represents C2-C10 alkyl, C1-C4 alkoxymethyl, or C3-C10 cycloalkyl; R represents halogen, C1-C4 alkyl, C1-C4 haloalkyl or C1-C4 alkoxy; n represents a number between 1 and 5; Y represents halogen, cyano, C1-C4 alkyl or C1-C4 alkoxy; whereby * is a chirality centre with an R-configuration. The invention also relates to a method for producing said compounds, to agents containing the compounds and to the use thereof for combating harmful fungi.