Antipsychotics

Application Reactant involved in: Trifluoromethylation of arenes Nucleophilic addition followed by intramolecular aza-Michael reactions Perfluoroalkylation of carbonyl compounds, aldimines and other organic substrates Used to prepare perfluoroalkyl

Application ( R )-(+)-3,3,3-Trifluoro-1,2-epoxypropane can be used as a substrate to synthesize: Substituted trifluoro amino propanols, which are found to be potent inhibitors of cholesteryl ester transfer protein. (2 R )

Application ( R )-(+)-&#945-Methoxy-&#945-trifluoromethylphenylacetic acid is commonly used as a derivatizing agent in Mosher ester analysis, an NMR-based method for determining the absolute configuration of the chiral carbon center in a

Application ( R )-(+)-&#945-Methoxy-&#945-trifluoromethylphenylacetic acid is commonly used as a derivatizing agent in Mosher ester analysis, an NMR-based method for determining the absolute configuration of the chiral carbon center in a

Application ( R )-(+)-&#945-Methoxy-&#945-trifluoromethylphenylacetic acid is commonly used as a derivatizing agent in Mosher ester analysis, an NMR-based method for determining the absolute configuration of the chiral carbon center in a

Application These enantiomerically pure (+)- and (&#8722)-2,2,2-trifluoro-1-(9-anthryl)ethanols have been used for the NMR spectral determination of optical purity (and in some cases, absolute configuration) of a wide variety of sulfoxides,

Application Highly selective organocatalyst for 1,3-dipolar addition and Friedel-Crafts alkylation. Legal Information U.

Application Highly selective organocatalyst for 1,3-dipolar addition and Friedel-Crafts alkylation. Legal Information U.

(R)-1,1,1-Trifluoro-2-propanol

(R)-1-Boc-3-methylpiperazine

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

(R)-3-Methyl-2-ketopiperazine