24706-89-6

Upstream product

• 1823-90-1 4-hydroxy-3,3-dimethyl-butan-2-one 
• 98-59-9 p-toluenesulfonyl chloride 
• 61674-96-2 4-(benzyloxy)-3,3-dimethylbutan-2-one 
• 3814-41-3 3-methylbut-2-en-2-yl acetate 
• 563-80-4 3-methyl-butan-2-one 

Downstream Products

• 86043-95-0 Toluene-4-sulfonic acid 3-[(Z)-benzyloxyimino]-2,2-dimethyl-butyl ester 
• 86043-95-0 3,3-dimethyl-4-<<(4-methylphenyl)sulfonyl>oxy>-2-butanone O-(phenylmethyl)oxime 
• 87070-46-0 (E)-3,3-dimethyl-4-<<(4-methylphenyl)sulfonyl>oxy>-2-butanone oxime 
• 106367-28-6 [3-Chloro-1,2,2-trimethyl-prop-(E)-ylidene]-phenyl-amine 
• 106367-27-5 Benzyl-[3-chloro-1,2,2-trimethyl-prop-(E)-ylidene]-amine 
• 106367-29-7 [3-Chloro-1,2,2-trimethyl-prop-(E)-ylidene]-(1-phenyl-ethyl)-amine 
• 80783-12-6 1-(4-chlorophenoxy)-2,2-dimethyl-butan-3-one 
• 86043-96-1 2,3,3-trimethyl-1-(phenylmethoxy)azetidine 
• 3329-43-9 2,2,3-trimethyl-but-3-en-1-ol 
• 23171-85-9 2,3,3-Trimethyl-2-pentanol 
• 36873-08-2 4-bromo-2,2-dimethyl-3-oxobutyl para-toluenesulfonate 

Relevant academic research and scientific papers

New macrocyclic bistriazolophanes with thioindigo chromophore

Bi(4-methoxycarbonyl-3-oxothiolan-2-ylidene) derivatives are prepared by oxidative dimerization of 4- oxotetrahydrothiophene-3-carboxylates with either TPAPeNMO or K3[Fe(CN)6]. The products are obtained as mixtures of four diastereoi

Synthesis of β-Chloroimines

β-Chloroimines 6 have been prepared from β-chlorocarbonyl compounds 5 by reaction with primary amines via two major approaches.

Combating fungi with substituted 1-azolyl-butan-2-ones and -2-ols

Substituted 1-azolyl-but-2-ones and -2-ols of the formula STR1 in which B is --CO-- or --CH(OH)-- Az represents a 1,2,4-triazol-1-yl or -4-yl or imidazol-1-yl radical, R1 represents a hydrogen atom, an alkyl, alkenyl, alkinyl, optionally substi

Antimicrobial agents and their use

The invention relates to pharmaceutical compositions containing an active antimicrobial compound of Formula (I). Also included in the invention are methods for combatting mycoses utilizing the above-identified pharmaceutical composition.

Combating fungi with novel 2-azolylmethyl-1,3-dioxolane and -dioxane derivatives

A 2-azolylmethyl-1,3-dioxolane or -dioxane derivative of the formula STR1 in which Az is imidazol-1-yl or 1,2,4-triazol-1-yl, R1, R2, R3 and R5 each independently is hydrogen or alkyl, or R1 and Rsup

4-Substituted 3,3-dimethyl-butan-2-ones, processes for their preparation and their use as intermediate products

4-substituted 3,3-dimethyl-butan-2-ones of the formula STR1 in which R represents cyano or the grouping --X--R1, wherein R1 represents n-alkyl with 1 to 4 carbon atoms, isopropyl, isobutyl, sec.-butyl, alkenyl with 3 to 4 carbon atom

Combating fungi with 4-substituted 1-azolyl-1-phenoxy-3,3-dimethyl-butan-2-ones and -ols

A fungicidally active 4-substituted-1-azolyl-1-phenoxy-3,3-dimethyl-butan-2-one or -ol of the formula STR1 in which A is a nitrogen atom or CH, B is --CO-- or CH(OH), R is cyano or X--R1, R1 is alkyl, optionally substituted aryl or o