116679-89-1

Upstream product

• 4252-78-2 2,2',4'-trichloroacetophenone 
• 288-88-0 1,2,4-Triazole 
• 41253-21-8 sodium triazole 
• 89058-45-7 4-(2,4-dichlorophenyl)pent-4-enal 
• 94855-19-3 1-Chloro-2-(2,4-dichloro-phenyl)-4-[1,3]dioxolan-2-yl-butan-2-ol 
• 98849-35-5 2-{2-[2-(2,4-Dichloro-phenyl)-oxiranyl]-ethyl}-[1,3]dioxolane 
• 67-56-1 methanol 
• 94855-20-6 1-(1,2,4-triazol-1-yl)-2-(2,4-dichlorophenyl)-4-(1,3-dioxolan-2-yl)butan-2-ol 

Relevant academic research and scientific papers

EXTENDED SCOPE OF THE GRIGNARD REACTION OF β-HALOACETALS. USE OF ACYCLIC ACETALS

Careful control of reaction conditions permits the high yield preparation of Grignard reagents fron β-halogenoacetals and their condensation with carbonyl compounds, regardless of the halogen (bromine, chlorine) or acetal structure (cyclic, acyclic).

Heterocyclic compounds

Triazoles and imidazoles of the formula (I): STR1 and stereoisomers thereof, wherein W is CH or N; Q is optionally substituted aryl (especially optionally substituted phenyl), optionally substituted aralkyl, or alkyl; R1 is H, alkyl, cycloalkyl