The chemical substance known as (2R,4S)-ethyl 5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoate, with the CAS number 752174-62-2, is a chiral compound characterized by its specific stereochemistry, indicated by the (2R,4S) configuration. This compound features an ethyl ester functional group, which contributes to its solubility and reactivity. The presence of a biphenyl moiety enhances its hydrophobic characteristics, potentially influencing its biological activity and interactions. The amino group in the structure suggests that it may participate in hydrogen bonding, which can affect its pharmacokinetic properties. Additionally, the branched alkyl chain (2-methylpentanoate) provides steric hindrance, which may impact its conformational flexibility. Overall, this compound's unique structural features suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, where stereochemistry plays a crucial role in biological activity and efficacy. Further studies would be necessary to explore its specific properties and potential uses in various chemical and biological contexts.

(2R,4S)-ethyl 5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoate

752174-62-2: The chemical substance known as (2R,4S)-ethyl 5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoate, with the CAS number 752174-62-2, is a chiral compound characterized by its specific stereochemistry, indicated by the (2R,4S) configuration. This compound features an ethyl ester functional group, which contributes to its solubility and reactivity. The presence of a biphenyl moiety enhances its hydrophobic characteristics, potentially influencing its biological activity and interactions. The amino group in the structure suggests that it may participate in hydrogen bonding, which can affect its pharmacokinetic properties. Additionally, the branched alkyl chain (2-methylpentanoate) provides steric hindrance, which may impact its conformational flexibility. Overall, this compound's unique structural features suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, where stereochemistry plays a crucial role in biological activity and efficacy. Further studies would be necessary to explore its specific properties and potential uses in various chemical and biological contexts.

CAS 752174-62-2

(2R,4S)-ethyl 5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoate

(2R,4S)-ETHYL 5-([1,1′-BIPHENYL]-4-YL)-4-AMINO-2-METHYLPENTANOATE

Ref: 10-F470011