摘要:
The present invention relates to N-(ortho-phenyl)-1-methyl-3-difluoromethylpyrazole-4-carboxanilides of the formula I in which the substituents are as defined below:R1 and R2 independently of one another are halogen, C1-C6-alkyl, C1-C6-haloalkyl, cyano, nitro, methoxy, trifluoromethoxy or difluoromethoxy.
摘要:
The invention relates to 5,6-cycloalkyl-7-aminotriazolopyrimidines of formula (I), where X=alkylene or alkenylene, whereby the carbon chain can be interrupted by one or two heteroatoms selected from S, O or NR1, R1═H, alkyl or C(═O)alkyl, L=halogen, cyano, nitro, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, alkinyl or NR2R3; R2,R3=each one of the groups given for R1 and m=a whole number from 0 to 5, whereby the aliphatic groups can be substituted by one to three of the following groups: halogen, cyano, nitro, hydroxy, alkoxy, alkylthio, or NRaRb, where Ra, Rb═H or alkyl in which the carbon chains can be halogenated. The invention further relates to methods for production of said compounds, agents comprising the same and use thereof for the prevention of fungal pests harmful to plants.
摘要翻译:本发明涉及式(I)的5,6-环烷基-7-氨基三唑并嘧啶,其中X =亚烷基或亚烯基,其中碳链可被一个或两个选自S,O或NR 1的杂原子中断, 卤素,氰基,硝基,烷基,卤代烷基,烷氧基,卤代烷氧基,烯基,炔基或NR 2(O) 3 SUP> 3 SUP> R 2,R 3 =每个给定R 1的基团,m = 0至5的整数,由此脂族基 基团可以被一至三个以下基团取代:卤素,氰基,硝基,羟基,烷氧基,烷硫基或NR a R b,其中R 0, 或其中碳链可以被卤化的烷基。 本发明还涉及生产所述化合物的方法,包含该化合物的试剂及其用于预防对植物有害的真菌害虫的用途。
摘要:
The use of substituted triazolopyrimidines of the formula I in which R1 is alkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle comprising one to four heteroatoms from the group consisting of O, N and S, R2 is hydrogen or a group R1, where R1 and/or R2 may be substituted according to the description, and X is halogen; as fungicides, novel 6-(2-tolyl)triazolopyrimidines, processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
摘要:
The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R1 represents alkyl or alkoxyalkyl; R2 represents alkyl, R1 and/or R2 being substituted according to the description. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.
摘要翻译:本发明涉及式(I)的5,6-二烷基-7-氨基 - 三唑并嘧啶,其中取代基定义如下:R 1表示烷基或烷氧基烷基; R 2表示根据描述被取代的烷基,R 1和/或R 2 O 2。 本发明还涉及一种生产所述化合物的方法,含有后者的药剂及其用于控制植物致病真菌的用途。
摘要:
Triazolopyrimidines of the formula I in which the substituents are as defined below: R1, R2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S, R1 and R2 together with the nitrogen atom to which they are attached may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and may contain a further heteroatom from the group consisting of O, N and S as ring member and may be substituted as defined in the description; L is halogen, cyano, alkyl, haloalkyl, alkoxy, alkenyloxy or alkoxycarbonyl; m is 1, 2, 3 or 4, where the groups L may be different if m is greater than 1; X is halogen, cyano, alkyl, haloalkyl, alkoxy or haloalkoxy; Processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi
摘要:
Pyrimidines of the formula I in which Ln is as defined in the description and the substituents R1, R2 and R3 are as defined below: R1 is C1-C10-alkyl, C2-C10-alkenyl, C2-C10-alkynyl, C3-C12-cycloalkyl, C3-C10-cycloalkenyl, phenyl or a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which is attached via carbon and contains one to four heteroatoms from the group consisting of O, N and S; R2 is halogen, cyano, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-alkoxy, C3-C4-alkenyloxy or C3-C4-alkynyloxy, where the alkyl, alkenyl and alkynyl radicals of R2 may be substituted by halogen, cyano, nitro, C1-C2-alkoxy or C1-C4-alkoxycarbonyl; R3 is a five- or six-membered saturated, partially unsaturated or aromatic mono- or bicyclic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S; and processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi are described.
摘要:
Metered-dose aerosol inhaler composition, which contains a) at least one pharmaceutical active ingredient, b) at least one propellant, c) at least one native or modified cyclodextrine, d) at least one hydrophilic additive, and optionally ethanol; process for the preparation of a metered-dose aerosol inhaler composition; as well as the use of a combination of cyclodextrine with a hydrophilic additive as suspension stabilizer in a metered-dose aerosol inhaler.
摘要:
A measuring system is disclosed for the detection, the manipulation and the output of medical measured values which includes a computer, an input interface (2) for the connection of measuring probes (3, 4, 5), an output interface (6) for further manipulation of the measuring data detected by the measuring probes (3, 4, 5) as well as a signal output device (7), wherein the computer is connected to the input interface (2), the output interface (6) as well as to the signal output device (7). In addition, the computer includes a device for automatic recognition of a particular embodiment from a plurality of different predetermined embodiments of measuring probes (3, 4, 5) with the connection of a measuring probe (3, 4, 5) of a particular embodiment to the input interface (2) as well as a device connected therewith for reprogramming the computer as determined from the automatic recognition device.
摘要:
The combination of a fibrinolytic and a prostacyclin analogue is very useful for thrombosis treatment, especially to avoid subsequent rethrombosis.