146464-96-2

Upstream product

• 711-38-6 4'-methoxy-2,2,2-trifluoroacetophenone 
• 1530-45-6 (carbethoxymethyl)triphenylphosphonium bromide 
• 383-63-1 ethyl trifluoroacetate, 
• 7396-44-3 benzyl diethylphosphonoacetate 
• 14774-77-7 p-methoxyphenyllithium 
• 13139-86-1 4-methoxyphenyl magnesium bromide 

Downstream Products

• 146464-98-4 4,4,4-trifluoro-3-(4-methoxyphenyl)butanoic acid 
• 146465-04-5 Toluene-4-sulfonic acid 4,4,4-trifluoro-3-(4-hexyloxy-phenyl)-butyl ester 
• 146465-00-1 4,4,4-Trifluoro-3-(4-hexyloxy-phenyl)-butyric acid hexyl ester 
• 146465-01-2 4,4,4-Trifluoro-3-(4-hexyloxy-phenyl)-butyric acid 
• 146465-03-4 4,4,4-Trifluoro-3-(4-hexyloxy-phenyl)-butan-1-ol 
• 146464-99-5 4,4,4-Trifluoro-3-(4-hydroxy-phenyl)-butyric acid 
• 146464-97-3 ethyl 4,4,4-trifluoro-3-(4-methoxyphenyl)-2-butanoate 

Relevant academic research and scientific papers

Synthesis and Properties of Optically Active α-Trifluoromethylbenzyl Derivatives as New Chiral Dopants for Ferroelectric Liquid Crystals

Optically active α-trifluoromethylbenzyl derivatives as new chiral dopants for ferroelectric liquid crystals (FLCs) were synthesized utilizing optically active 4,4,4-trifluoro-3-(4-methoxyphenyl)butanoic acid prepared by optical resolution procedures.The

Convenient stereoselective synthesis of β-perfluoroalkyl α,β-unsaturated esters via H?rner-Wadsworth-Emmons reactions

Condensation of H?rner-Wadsworth-Emmons reagents 3 and ketones 2 with a perfluoroalkyl (Rf) moiety prepared in situ was proved to be significantly efficient and powerful methods for the construction of a wide variety of α,β-unsaturated esters with Rf and R1 groups both at the β-position due to convenient avoidance of usually tedious as well as troublesome isolation steps of these ketones 2.