55364-29-9

Upstream product

• 1373497-80-3 C₇H₁₅F₃O₃SSi 
• 2314-97-8 iodotrifluoromethane 
• 754-05-2 ethenyltrimethylsilane 

Downstream Products

• 78622-55-6 (E)-1-(3,3,3-trifluoroprop-1-enyl)-4-methoxybenzene 
• 1373497-84-7 (E)-1-methoxy-2-(3,3,3-trifluoroprop-1-en-1-yl)benzene 
• 1373497-81-4 (E)-1-isopropyl-4-(3,3,3-trifluoroprop-1-enyl)benzene 
• 1373497-86-9 ethyl (E)-4-(3,3,3-trifluoroprop-1-en-1-yl)benzoate 
• 1373497-82-5 (E)-methyl(4-(3,3,3-trifluoroprop-1-enyl)phenyl)sulfane 
• 1104449-20-8 (E)-1-(benzyloxy)-4-(3,3,3-trifluoroprop-1-en-1-yl)benzene 
• 1373497-85-8 (E)-1-(methoxymethoxy)-2-(3,3,3-trifluoroprop-1-enyl)benzene 
• 1373497-83-6 (E)-9-phenyl-3-(3,3,3-trifluoroprop-1-enyl)-9H-carbazole 
• 1357615-55-4 (E)-2-(3,3,3-trifluoroprop-1-en-1-yl)aniline 
• 1440779-46-3 (E)-4-chloro-2-(3,3,3-trifluoroprop-1-en-1-yl)aniline 
• 1440779-50-9 (E)-5-chloro-2-(3,3,3-trifluoroprop-1-en-1-yl)aniline 

Relevant academic research and scientific papers

Selective nickel-catalyzed fluoroalkylations of olefins

Mild and selective nickel-catalyzed trifluoromethylation and perfluoroalkylation reactions of alkenes were developed to provide fluorinated olefins, including natural products, pharmaceuticals, and variety of synthetic building blocks in good to excellent

Simple synthesis of β-trifluoromethylstyrenes using (E)-trimethyl-(3,3,3-trifluoroprop-1-enyl)silane

(E)-Trimethyl-(3,3,3-trifluoroprop-1-enyl)silane (1) was synthesized as a reagent for use in Hiyama cross-coupling reactions for the production of β-trifluoromethylstyrene derivatives. Cross-coupling of 1 with electronically diverse aryl iodides was achieved by treatment with CsF in the presence of catalytic amounts of palladium to afford the desired products in moderate to good yields.