(S)-(+)-4-Phenyl-2-butanol (CAS 22148-86-3)

(S)-(+)-4-Phenyl-2-butanol, a chiral secondary alcohol, is an intriguing compound for researchers due to its specific stereochemistry. This molecule features a four-carbon chain with a phenyl group attached to the fourth carbon, and an alcohol functional group at the second carbon, making it a valuable intermediate in the synthesis of complex organic molecules. Its (S)-configuration is particularly noteworthy, as it plays a role in the enantioselective synthesis processes, where the creation of stereochemically pure substances is required. The presence of the phenyl group enhances its reactivity and makes it a pivotal building block in the construction of aromatic compounds. This compound′s utility extends into various fields of chemistry research, including material science and catalysis, where its unique structure can influence the properties and reactivity of the synthesized materials. Its role in the development of chiral catalysts, ligands, and other stereochemically complex structures is of particular interest, demonstrating its versatility and importance in advancing the frontiers of chemical research. Moreover, (S)-(+)-4-Phenyl-2-butanol acts as a solvent in organic reactions. Animal studies indicate its potential to reduce inflammation and alleviate pain (anti-nociceptive effects). Furthermore, cell culture studies reveal its antioxidant and anti-cancer properties. (S)-(+)-4-Phenyl-2-butanol also inhibits cyclooxygenase-2 (COX-2), an enzyme involved in prostaglandin production.