CAS 131320-21-3

(S)-1-(4-bromophenyl)propan-1-ol is an organic compound characterized by its chiral structure, featuring a bromophenyl group attached to a propanol backbone. The presence of the bromine atom on the phenyl ring significantly influences its chemical properties, including reactivity and polarity. This compound is typically a colorless to pale yellow liquid at room temperature and is soluble in organic solvents, while its solubility in water is limited due to the hydrophobic nature of the bromophenyl moiety. The chiral center at the propanol position allows for the existence of enantiomers, with the (S)-configuration being one specific stereoisomer. This compound may exhibit interesting biological activities, making it of interest in medicinal chemistry and pharmaceutical research. Its synthesis often involves the use of chiral catalysts or reagents to ensure the desired stereochemistry is achieved. Additionally, the presence of the bromine atom can facilitate further chemical modifications, making it a versatile intermediate in organic synthesis.