110929-41-4

Upstream product

• 108-98-5 thiophenol 
• 34509-09-6 1,1,1-trifluoro-3-(phenylthio)propan-2-one 
• 100-68-5 methyl-phenyl-thioether 
• 88790-04-9 2-hydroxy-3,3,3-trifluoropropyl phenyl sulfide 
• 75-36-5 acetyl chloride 

Downstream Products

• 110929-54-9 (2S)-(-)-3,3,3-Trifluoro-1-phenylthio-2-propanol 
• 110929-55-0 (S)-2-acetoxy-1,1,1-trifluoro-3-(phenylthio)propane 

Relevant academic research and scientific papers

Highly stereocontrolled access to 1,1,1-trifluoro-2,3-epoxypropane via lipase-mediated kinetic resolution of 1,1,1-trifluoro-3-(phenylthio)propan-2-ol and its application

1,1,1-Trifluoro-3-(phenylthio)propan-2-ol was prepared in high enantiomeric purity by lipase-mediated kinetic resolution of the corresponding esters. The resolved alcohol was successfully converted into 1,1,1 -trifluoro-2,3-epoxypropane and/or used in the

Anodic methoxylation of 2-acyloxy-3,3,3-trifluoropropyl sulfides accompanying with [1,2]-rearrangement of the acyloxy group and anodic cyclization of 2-(t-butoxycarbonyl)oxy-3,3,3-trifluoropropyl sulfide

Anodic methoxylation of 2-acyloxy-3,3,3-trifluoropropyl sulfides was carried out in methanol containing Et3N-3HF as a supporting electrolyte and mediator using an undivided cell to provide the corresponding α-methoxylated products and unexpecte