摘要:
The present invention relates to active compound combinations of a fluorobenzo-thiazole of the formula (I) and at least one of the compounds listed herein. The active compound combinations of the present invention are useful as fungicides.
摘要:
The invention relates to novel fungicidally active compound combinations of (a) methoximinoacetamide derivatives of the general formula (I), in which R1 represents unsubstituted or fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i- or t-butyl-, methoxy-, ethoxy-, or phenoxy-substituted phenyl, 2-naphthyl, 1,2,3,4-tetrahydronaphthyl, indanyl, 2-benzofuranyl, 2-benzothienyl, 2-thienyl, or 2-furanyl, and (b) the active compound groups (I) to (58) listed in the disclosure.
摘要:
Aza-heterocycloalkenes of the formula (I): wherein Z, G, Ar, E, y1, A and Y2 are as described herein are useful for combating pests, particularly fungi. Processes for preparing the compounds of formula (I) are also disclosed, along with intermediates useful therein.
摘要:
The present invention relates to fungicidally active compound combinations of a fluorobenzothiazole derivative of the formula (I) and at least one of the compounds listed in the disclosure.
摘要:
Pyrazolopyrimidines of the formula in which R1, R2, R3, R4, R5 and X are as defined in the description, processes for preparing these compounds and their use for controlling unwanted microorganisms.
摘要:
Pyrazolopyrimidines of the formula in which R1, R2, R3, R4, R5 and X are as defined in the description, processes for preparing these compounds and their use for controlling unwanted microorganisms.
摘要:
The present invention relates to fungicidally active compound combinations of a fluorobenzothiazole derivative of the formula (I) and at least one of the compounds listed in the disclosure.
摘要:
The present invention relates to novel N-alkoxy-arnidine derivatives of the formula (I), to a process for their preparation and to their use as pesticides. In addition, the invention also relates to novel intermediates and to a process for their preparation. ##STR1##
摘要:
Process for the preparation of pyrazole from hydrazine hydrate and acrolein comprising reacting hydrazine hydrate with acrolein in an aqueous-organic medium at a temperature between 20.degree.-80.degree. C. and then oxidizing the 2-pyrazoline formed, of the formula ##STR1## either directly or after first being isolated, with chlorine or an alkali metal hypochlorite or an alkaline earth metal hypochlorite and water or an aqueous-organic medium at a temperature between 0.degree. and 60.degree. C.
摘要:
Process for the preparation of pyrazole by heating a pyrazoline derivative of the general formula ##STR1## in which R represents an optionally substituted phenyl radical, or an alkyl or halogenoalkyl radical, without the addition of an acid or base, at a temperature between 100.degree. and 200.degree. C. under a pressure between 1 mbar and 10 bars, optionally in the presence of a diluent.