112298-06-3

Upstream product

• 637-59-2 1-Bromo-3-phenylpropane 
• 85674-68-6 1,1,1-trifluoro-5-phenyl-pentan-2-one 

Downstream Products

• 112298-08-5 5-phenyl-1,1,1-trifluoropentan-2-ol triflate 
• 85674-68-6 1,1,1-trifluoro-5-phenyl-pentan-2-one 
• 112298-25-6 2-methyl-5-phenyl-1,1,1-trifluoropentane-2-ol triflate 
• 112298-27-8 2-(hexafluoroisopropoxy)-5-phenyl-2-(trifluoromethyl)-pentane 
• 112298-26-7 5-phenyl-2-(trifluoroacetoxy)-2-(trifluoromethyl)pentane 
• 112298-41-6 5-phenyl-2-(trifluoromethyl)pent-1-ene 
• 129049-14-5 5-phenyl-2-(trifluoromethyl)pent-2-ene 
• 112298-12-1 5-phenyl-2-(trifluoroacetoxy)-1,1,1-trifluoropentane 
• 112298-07-4 5-phenyl-1,1,1-trifluoropentan-2-ol tosylate 
• 112298-23-4 2-methyl-5-phenyl-1,1,1-trifluoropentan-2-ol 

Relevant academic research and scientific papers

Optically active aromatic compounds, preparation process thereof, and liquid crystal compositions and elements

Disclosed in the present invention are the optically active aromatic compounds having a trifluoromethyl group useful as a component of ferroelectric liquid crystal compositions, a process for preparing the above compounds, liquid crystal compositions havi

Access to Trifluoromethylindanes; Cycloalkylation of β-Phenyl Trifluoromethyl Ketones, β-Keto Esters, and Alcohols

Cycloalkylation of β-phenyl trifluoromethyl ketones, β-keto esters, and alcohols provides indanic compounds bearing a CF3 group.

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