The chemical substance known as (1S,2R)-2-{benzyl[(2,4,6-trimethylphenyl)sulfonyl]amino}-1-phenylpropyl acetate, with the CAS number 240423-53-4, is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a chiral center, indicated by the (1S,2R) configuration, which contributes to its potential biological activity and interactions. The presence of a benzyl group and a sulfonamide moiety suggests that it may exhibit significant pharmacological properties, possibly acting as an inhibitor or modulator in various biochemical pathways. The acetate functional group indicates that it may participate in esterification reactions or hydrolysis, influencing its solubility and reactivity. Additionally, the presence of multiple aromatic rings, particularly the 2,4,6-trimethylphenyl group, suggests that the compound may have substantial lipophilicity, affecting its distribution in biological systems. Overall, this compound's unique structural features may render it of interest in medicinal chemistry and drug development.

(1S,2R)-2-{benzyl[(2,4,6-trimethylphenyl)sulfonyl]amino}-1-phenylpropyl acetate

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(1S,2R)-2-(N-Benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl acetate

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CAS 240423-53-4: (1S,2R)-2-{benzyl[(2,4,6-trimethylphenyl)sulfonyl]amino}-1-phenylpropyl acetate

(1S,2R)-2-(N-Benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl acetate

Ref: IN-DA003BIE

Acetic Acid (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenylpropyl Ester

Ref: 3D-FA59930

Acetic Acid (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenylpropyl Ester [Reagent for double aldol reaction]

Ref: 3B-A1535