(S)-3-(4-Chlorophenyl)-beta-alaninol HCl is a chiral compound characterized by its beta-alanine structure, which includes a beta-amino acid moiety. The presence of the 4-chlorophenyl group contributes to its hydrophobic characteristics, potentially influencing its biological activity and interactions. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in pharmaceutical applications. The compound's chirality indicates that it exists in two enantiomeric forms, with the (S)-configuration often being associated with specific biological activities. This compound may be of interest in medicinal chemistry, particularly in the development of drugs targeting neurological or metabolic pathways. Its properties, such as melting point, solubility, and stability, would be influenced by the presence of the hydrochloride group and the chlorophenyl substituent. Overall, (S)-3-(4-chlorophenyl)-beta-alaninol HCl represents a significant structure for further research in drug development and biochemical applications.

(S)-3-(4-CHLOROPHENYL)-BETA-ALANINOL HCL

1590388-37-6: (S)-3-(4-Chlorophenyl)-beta-alaninol HCl is a chiral compound characterized by its beta-alanine structure, which includes a beta-amino acid moiety. The presence of the 4-chlorophenyl group contributes to its hydrophobic characteristics, potentially influencing its biological activity and interactions. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in pharmaceutical applications. The compound's chirality indicates that it exists in two enantiomeric forms, with the (S)-configuration often being associated with specific biological activities. This compound may be of interest in medicinal chemistry, particularly in the development of drugs targeting neurological or metabolic pathways. Its properties, such as melting point, solubility, and stability, would be influenced by the presence of the hydrochloride group and the chlorophenyl substituent. Overall, (S)-3-(4-chlorophenyl)-beta-alaninol HCl represents a significant structure for further research in drug development and biochemical applications.

<p>(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol hydrochloride</p>

CAS 1590388-37-6

(S)-3-(4-CHLOROPHENYL)-BETA-ALANINOL HCL

(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol hydrochloride

Ref: 54-OR1005777

(S)-3-(4-CHLOROPHENYL)-β-ALANINOL HCL

Ref: 10-F302749