A new application about (1R,2S)-(−)-2-Amino-1,2-diphenylethanol

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Formula: C6H5CH(NH2)CH(C6H5)OH, you can also check out more blogs about23190-16-1

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.23190-16-1, Name is (1R,2S)-(−)-2-Amino-1,2-diphenylethanol, molecular formula is C6H5CH(NH2)CH(C6H5)OH. In a Article,once mentioned of 23190-16-1, Formula: C6H5CH(NH2)CH(C6H5)OH

Novel chemically bonded chiral stationary phases (CSP’s) derived from (1R,2S)-2-carboxymethylamino-1,2-diphenylethanol and from (1S,2S)-2-carboxymethylamino-1,2-diphenylethanol were prepared.The ligand exchange chromatography on these CSP’s was found to be effective for the direct resolution of the enantiomers of amino acids.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Formula: C6H5CH(NH2)CH(C6H5)OH, you can also check out more blogs about23190-16-1

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare