1,2-Ethanediol, 1,1,2-triphenyl-, 2-acetate, (2S)-


Chemical Name: 1,2-Ethanediol, 1,1,2-triphenyl-, 2-acetate, (2S)-
CAS Number: 95061-51-1
Product Number: AG003AYO(AGN-PC-0W4MIN)
Synonyms:
MDL No:
Molecular Formula: C22H20O3
Molecular Weight: 332.3924

Identification/Properties


Properties
MP:
246-249 °C
BP:
487.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(S)-2-Hydroxy-1,2,2-triphenylethyl acetate, also known as chiral BINOL-derived ester, is a valuable compound widely used in chemical synthesis as a chiral building block. With its unique stereochemical properties, this compound plays a crucial role in asymmetric synthesis and catalysis.In chemical synthesis, (S)-2-Hydroxy-1,2,2-triphenylethyl acetate serves as a key chiral intermediate for the preparation of various chiral compounds and pharmaceuticals. Its presence enables the asymmetric induction of specific configurations during reactions, leading to the synthesis of enantiomerically pure products. This compound is particularly useful in the production of drugs, agrochemicals, and specialty chemicals where chirality is a critical factor in determining biological activity or physical properties.Moreover, (S)-2-Hydroxy-1,2,2-triphenylethyl acetate is often employed as a versatile ligand in transition metal-catalyzed reactions, such as asymmetric hydrogenation, asymmetric allylation, and asymmetric epoxidation. By forming complexes with transition metal catalysts, this compound facilitates selective bond formation, enabling chemists to achieve high yields of enantiomerically enriched products.Overall, the application of (S)-2-Hydroxy-1,2,2-triphenylethyl acetate in chemical synthesis is instrumental in the production of chiral molecules with precise stereochemistry, making it an essential tool for modern organic synthesis and drug development.