(S)-4-hydroxymandelic acid, with the CAS number 13244-75-2, is an organic compound characterized by its chiral nature, featuring a hydroxyl group and a carboxylic acid functional group. It is a derivative of mandelic acid, specifically the S-enantiomer, which is significant in various biochemical applications. This compound typically appears as a white crystalline solid and is soluble in water due to the presence of polar functional groups. Its molecular structure includes a phenyl group attached to a carbon chain that contains both a hydroxyl (-OH) and a carboxylic acid (-COOH) group, contributing to its acidic properties. (S)-4-hydroxymandelic acid is of interest in pharmaceutical research and may play a role in metabolic pathways, particularly in the context of catecholamine metabolism. Additionally, it can serve as a chiral building block in organic synthesis, highlighting its importance in the development of enantiomerically pure compounds. Overall, its unique structural features and biological relevance make it a compound of interest in both chemistry and biochemistry.

(S)-4-hydroxymandelic acid

13244-75-2: (S)-4-hydroxymandelic acid, with the CAS number 13244-75-2, is an organic compound characterized by its chiral nature, featuring a hydroxyl group and a carboxylic acid functional group. It is a derivative of mandelic acid, specifically the S-enantiomer, which is significant in various biochemical applications. This compound typically appears as a white crystalline solid and is soluble in water due to the presence of polar functional groups. Its molecular structure includes a phenyl group attached to a carbon chain that contains both a hydroxyl (-OH) and a carboxylic acid (-COOH) group, contributing to its acidic properties. (S)-4-hydroxymandelic acid is of interest in pharmaceutical research and may play a role in metabolic pathways, particularly in the context of catecholamine metabolism. Additionally, it can serve as a chiral building block in organic synthesis, highlighting its importance in the development of enantiomerically pure compounds. Overall, its unique structural features and biological relevance make it a compound of interest in both chemistry and biochemistry.

CAS 13244-75-2

(S)-4-hydroxymandelic acid