84877-47-4

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 10531-50-7 (R)-2,2,2-trifluoro-1-phenylethanol 
• 421-83-0 trifluoromethane sulfonyl chloride 

Downstream Products

• 881392-75-2 (2S)-4-methyl-2-(2,2,2-trifluoro-1S-phenyl-ethylamino)-pentanoic acid methyl ester 
• 62197-92-6 (αS)-α-(trifluoromethyl)-N-[(S)-1-phenylethyl]benzenemethanamine 
• 880762-37-8 2(R)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino]-3-tritylsulfanyl-propionic acid 
• 880762-38-9 2(R)-[2,2,2-trifluoro-1(R)-(4-fluorophenyl)ethylamino]-3-tritylsulfanyl-propionic acid 

Relevant academic research and scientific papers

Nucleophilic displacements of non-racemic α-trifluoromethyl benzylic triflates

Effective protocols for the introduction of chiral α-trifluoromethyl benzyl moieties by nucleophilic displacement of enantiomerically enriched α-trifluoromethyl benzylic triflates are presented. The effects of substrate electronics, solvent polarity, temp

Solvolysis of 1-Aryl-2,2,2-trifluoroethyl Sulfonates. Kinetic and Stereochemical Effects in the Generation of Highly Electron-Deficient Carbocations

Solvolysis rates of sulfonates XC6H4CH(O3SR)CF3 (R = p-Tol or CF3) correlate with ?+(X) with values of ρ+ between -6.7 and -11.9 depending upon solvent.For the tosylates the rates depend on the solvent parameter YOTs with