14856-93-0

Basic information

• Product Name: Benzene, [(pentafluoroethyl)sulfonyl]-
• CAS NO: 14856-93-0
• Molecular Formula: C8H5F5O2S
• Molecular Weight: 260.185
• Mol File: 14856-93-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzene, [(pentafluoroethyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(pentafluoroethyl)sulfonyl]-(14856-93-0)
• EPA Substance Registry System: Benzene, [(pentafluoroethyl)sulfonyl]-(14856-93-0)

Safety Data

• Hazardous Substances Data: 14856-93-0(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 65538-00-3 phenyl pentafluoroethyl sulfide 

Downstream Products

• 1231728-72-5 α-(3-nitrophenyl)-α-(pentafluoroethyl)-benzenemethanol 
• 722491-64-7 4-methoxy-α-(4-methoxyphenyl)-α-(pentafluoroethyl)-benzenemethanol 
• 1231728-66-7 N-(1-(4-methylphenyl)-3,3,3,2,2-pentafluoropropyl)aniline 
• 1231728-70-3 N-[1-(t-butyl)-3,3,3,2,2-pentafluoropropyl]aniline 
• 1231728-63-4 N-[1-(4-fluorophenyl)-3,3,3,2,2-pentafluoropropyl]aniline 
• 1231728-68-9 N-[1-(2,4-dichlorophenyl)-3,3,3,2,2-pentafluoropropyl]aniline 
• 345-40-4 2,2,3,3,3-Pentafluoro-1-phenyl-propan-1-ol 
• 1231728-64-5 N-[1-(4-chlorophenyl)-3,3,3,2,2-pentafluoropropyl]aniline 
• 1231728-61-2 N-[1-(2-fluorophenyl)-3,3,3,2,2-pentafluoropropyl]aniline 
• 56184-56-6 4,4,5,5,5-pentafluoro-1-phenyl-1-penten-3-ol 
• 1231728-67-8 N-[1-(4-methoxyphenyl)-3,3,3,2,2-pentafluoropropyl]aniline 
• 357-51-7 4-chloro-α-(4-chlorophenyl)-α-(pentafluoroethyl)-benzenemethanol 
• 1231728-69-0 N-(1-cyclohexyl-3,3,3,2,2-pentafluoropropyl)aniline 
• 1231728-65-6 N-[1-(4-bromophenyl)-3,3,3,2,2-pentafluoropropyl]aniline 

Relevant articles and documents

Nucleophilic perfluoroalkylation of imines and carbonyls: Perfluoroalkyl sulfones as efficient perfluoroalkyl-transfer motifs

Alkoxide-induced nucleophilic pentafluoroethylation and trifluoromethylation of aldehydes, ketones, and imines using pentafluoroethyl phenyl sulfone (PhSO2CF2CF3, 1) and trifluoromethyl phenyl sulfone (PhSO2CF3, 2), respectively, have been successfully achieved. High diastereoselectivity was observed during the perfluoroalkylation of homochiral sulfinimines to give the corresponding perfluoroalkyl sulfinamides.