Methyl (3S)-4-chloro-3-hydroxybutanoate 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 chlorine atom at the fourth carbon contributes to its reactivity and potential applications in organic synthesis. The hydroxyl group (-OH) at the third carbon enhances its polarity, making it more soluble in polar solvents. This compound is typically used in chemical synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its molecular structure suggests that it may participate in various chemical reactions, including esterification and substitution reactions. Safety data should be consulted for handling and storage, as halogenated compounds can exhibit toxicity and environmental concerns. Overall, methyl (3S)-4-chloro-3-hydroxybutanoate is a versatile compound with significant implications in synthetic organic chemistry.

methyl (3S)-4-chloro-3-hydroxybutanoate

86728-93-0: Methyl (3S)-4-chloro-3-hydroxybutanoate 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 chlorine atom at the fourth carbon contributes to its reactivity and potential applications in organic synthesis. The hydroxyl group (-OH) at the third carbon enhances its polarity, making it more soluble in polar solvents. This compound is typically used in chemical synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its molecular structure suggests that it may participate in various chemical reactions, including esterification and substitution reactions. Safety data should be consulted for handling and storage, as halogenated compounds can exhibit toxicity and environmental concerns. Overall, methyl (3S)-4-chloro-3-hydroxybutanoate is a versatile compound with significant implications in synthetic organic chemistry.

CAS 86728-93-0

methyl (3S)-4-chloro-3-hydroxybutanoate

Butanoic acid,4-chloro-3-hydroxy-, methyl ester, (3S)-

Ref: IN-DA004NG2

(S)-Methyl-4-chloro-3-hydroxybutyrate

Ref: 54-OR912719