Ethyl (3S)-4-bromo-3-hydroxybutanoate, with the CAS number 95537-36-3, is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a chiral center at the third carbon, indicating that it exists in a specific stereoisomeric form, specifically the (3S) configuration. The presence of a bromine atom at the fourth carbon enhances its reactivity, making it useful in various synthetic applications, particularly in organic synthesis and medicinal chemistry. The hydroxy group at the third carbon contributes to its polarity, influencing its solubility in polar solvents. Ethyl (3S)-4-bromo-3-hydroxybutanoate can participate in nucleophilic substitution reactions due to the electrophilic nature of the bromine atom, and it may also undergo esterification or hydrolysis under appropriate conditions. Its unique structure and functional groups make it a valuable intermediate in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals.

Ethyl (3S)-4-bromo-3-hydroxybutanoate

95537-36-3: (-)-Ethyl 4-bromo-3-hydroxybutyrate, (S)-4-Bromo-3-hydroxybutanoic acid ethyl ester, Butanoic acid, 4-bromo-3-hydroxy-, ethyl ester, (S)-, Ethyl (3S)-4-bromo-3-hydroxybutanoate, butanoic acid, 4-bromo-3-hydroxy-, ethyl ester, (3S)-

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CAS 95537-36-3: Ethyl (3S)-4-bromo-3-hydroxybutanoate

(S)-Ethyl 4-bromo-3-hydroxybutanoate

Ref: 3D-VDA53736

(S)-Ethyl 4-bromo-3-hydroxybutanoate

Ref: IN-DA003PZV