(3S)-4-Benzyloxybutane-1,3-diol, with the CAS number 85418-23-1, is an organic compound characterized by its specific stereochemistry and functional groups. It features a butane backbone with a hydroxyl (-OH) group at the first and third positions, contributing to its diol classification. The presence of a benzyloxy group at the fourth position enhances its reactivity and solubility in organic solvents. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. Its stereochemistry, indicated by the (3S) designation, suggests that it has specific spatial arrangements that can influence its biological activity and interactions with other molecules. As a diol, it can participate in hydrogen bonding, making it useful in various chemical reactions, including esterification and etherification. Additionally, its structural features may allow it to act as a chiral building block in synthetic organic chemistry, particularly in the development of pharmaceuticals and other fine chemicals.

(3S)-4-benzyloxybutane-1,3-diol

85418-23-1: (3S)-4-(Benzyloxy)butane-1,3-diol, 1,3-butanediol, 4-(phenylmethoxy)-, (3S)-

(S)-4-(benzyloxy)butane-1,3-diol

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CAS 85418-23-1: (3S)-4-benzyloxybutane-1,3-diol

(S)-4-(benzyloxy)butane-1,3-diol

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(S)-4-Benzyloxy-1,3-butanediol

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(S)-4-Benzyloxy-1,3-butanediol

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