29279-80-9

Upstream product

• 402-51-7 4-(trifluoromethyl)phenylmagnesium bromide 
• 141-78-6 ethyl acetate 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 21221-91-0 4,4'-bis(trifluoromethyl)benzophenone 

Downstream Products

• 56860-29-8 1,1-bis(p-(trifluoromethyl)phenyl)cyclopropane 
• 56860-27-6 1,1-bis(p-(trifluoromethyl)phenyl)propene 
• 86043-02-9 1--5-trifluoromethylindan 
• 1335101-71-7 1,1-dibromo-2,2-bis(4-trifluoromethylphenyl)cyclopropane 
• 1335101-70-6 C₁₈H₁₂F₆ 
• 1335101-72-8 1-bromo-1-methyl-2,2-bis(4-trifluoromethylphenyl)cyclopropane 
• 1335101-67-1 2,2-bis(4-trifluoromethylphenyl)-1-methylenecyclopropane 
• 23349-14-6 4,4'-(2-bromoethene-1,1-diyl)bis((trifluoromethyl)benzene) 
• 1002128-05-3 ethyl 3,3-bis(4-(trifluoromethyl)phenyl)acrylate 

Relevant academic research and scientific papers

Halogenation of 1,1-diarylethylenes by N-halosuccinimides

An efficient method for the preparation of 2,2-diarylvinyl halides from the corresponding 1,1-diarylethylenes has been developed. N-Halosuccinimides (N-bromosuccinimide or N-chlorosuccinimide) were used as the halogenation reagents. The practicability of this method is highlighted by its simple operation, broad substrate scope and capability for large-scale reaction.