Archives for Chemistry Experiments of (1R,2S)-(−)-2-Amino-1,2-diphenylethanol

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of (1R,2S)-(−)-2-Amino-1,2-diphenylethanol. In my other articles, you can also check out more blogs about 23190-16-1

23190-16-1, Name is (1R,2S)-(−)-2-Amino-1,2-diphenylethanol, molecular formula is C6H5CH(NH2)CH(C6H5)OH, belongs to chiral-catalyst compound, is a common compound. In a patnet, once mentioned the new application about 23190-16-1, Application In Synthesis of (1R,2S)-(−)-2-Amino-1,2-diphenylethanol

Coordination of a chiral substrate to (meso-salen)cobalt(II) nitrate and subsequent oxidation generates a Co(III) complex exhibiting a strong chiroptical readout that is attributed to spontaneous substrate-to-ligand chirality imprinting. The characteristic circular dichroism (CD) response of the (salen)cobalt complex can be used for enantiomeric analysis of a variety of chiral substrates based on a simple CD measurement at low concentration and without additional purification steps. This chirality sensing approach has potential for high-throughput enantiomeric excess (ee) screening applications and minimizes solvent waste production. Copyright

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of (1R,2S)-(−)-2-Amino-1,2-diphenylethanol. In my other articles, you can also check out more blogs about 23190-16-1

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare