The chemical substance known as (2S,3S)-3-(Benzyloxycarbonylamino)-1-chloro-2-hydroxy-4-phenylbutane, with the CAS number 128018-43-9, is a chiral compound featuring multiple functional groups, including a benzyloxycarbonylamino group, a hydroxyl group, and a chloro substituent. Its structure indicates that it is a derivative of a phenylbutane, which contributes to its potential biological activity. The presence of the chiral centers at the 2 and 3 positions suggests that it may exhibit stereoisomerism, which can significantly influence its pharmacological properties. The benzyloxycarbonyl group is often used in peptide chemistry as a protective group, indicating potential applications in the synthesis of peptide-based drugs. The compound's hydrophilic hydroxyl group and hydrophobic phenyl group may affect its solubility and interaction with biological membranes. Overall, this compound may be of interest in medicinal chemistry and drug development, particularly in the context of designing compounds with specific stereochemical configurations for targeted biological activity.

(2S,3S)-3-(Benzyloxycarbonylamino)-1-chloro-2-hydroxy-4-phenylbutane

128018-43-9: The chemical substance known as (2S,3S)-3-(Benzyloxycarbonylamino)-1-chloro-2-hydroxy-4-phenylbutane, with the CAS number 128018-43-9, is a chiral compound featuring multiple functional groups, including a benzyloxycarbonylamino group, a hydroxyl group, and a chloro substituent. Its structure indicates that it is a derivative of a phenylbutane, which contributes to its potential biological activity. The presence of the chiral centers at the 2 and 3 positions suggests that it may exhibit stereoisomerism, which can significantly influence its pharmacological properties. The benzyloxycarbonyl group is often used in peptide chemistry as a protective group, indicating potential applications in the synthesis of peptide-based drugs. The compound's hydrophilic hydroxyl group and hydrophobic phenyl group may affect its solubility and interaction with biological membranes. Overall, this compound may be of interest in medicinal chemistry and drug development, particularly in the context of designing compounds with specific stereochemical configurations for targeted biological activity.

CAS 128018-43-9

(2S,3S)-3-(Benzyloxycarbonylamino)-1-chloro-2-hydroxy-4-phenylbutane

Benzyl ((2S,3S)-4-chloro-3-hydroxy-1-phenylbutan-2-yl)carbamate

Ref: IN-DA000XOR

Fosamprenavir Impurity 12

Ref: 4Z-F-1519