112298-30-3

Upstream product

• 112298-15-4 5-(p-chlorophenyl)-1,1,1-trifluoropentan-2-ol 
• 64473-35-4 3-(4-chlorophenyl)propyl bromide 

Downstream Products

• 112298-11-0 5-(p-chlorophenyl)-1,1,1-trifluoropentan-2-ol triflate 
• 112298-36-9 7-chloro-1-phenyl-1-(trifluoromethyl)-1,2,3,4-tetrahydronaphthalene 
• 112481-86-4 1-Trifluoromethyl-1-hydroxy-7-chloro-1,2,3,4-tetrahydronaphthalene 
• 112481-83-1 1,7-Dichloro-1-trifluoromethyl-1,2,3,4-tetrahydro-naphthalene 
• 112298-15-4 5-(p-chlorophenyl)-1,1,1-trifluoropentan-2-ol 
• 112298-18-7 5-(p-chlorophenyl)-2-phenyl-1,1,1-trifluoropentan-2-ol 

Relevant academic research and scientific papers

New catalytic oxidation of trifluoromethyl carbinols by a ruthenium(II) complex

The first catalytic oxidation of trifluoromethyl carbinols has been accomplished by a novel ruthenium(II) complex using sodium periodate as an oxidant. Trifluoromethyl ketones were obtained under mild conditions and in excellent yields. (C) 2000 Elsevier Science Ltd.

α-Trifluoromethyl-Destabilized Cations. A Route to 1-(Trifluoromethyl)tetralins by Trifluoroactolysis of 5-Aryl-1,1,1,-trifluoropentan-2-ols and Derivatives

Trifluoroacetolysis of 5-aryl-1,1,1-trifluoropentan-2-ols 1 and their 2-aryl (2) and 2-methyl (3) analogues has been studied in search of a route to 1-(trifluoromethyl)tetralins.The results reflect the relative stabilities of the incipient carbocation int