Ethyl (S)-4-Chloro-3-hydroxybutyrate TCI C1717

Chemical Identity

Other names: (S)-4-Chloro-3-hydroxybutyric Acid Ethyl Ester
CAS No.: 86728-85-0
PubChem: CID 7019277·SID 87566689
Formula: C6H11ClO3
Molecular weight: 166.60 g/mol
Purity: >95.0%(GC)
Storage: 0-10°C
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl (3S)-4-chloro-3-hydroxybutanoate
SMILES: CCOC(=O)CC(CCl)O
InChIKey: ZAJNMXDBJKCCAT-YFKPBYRVSA-N
MDL: MDL00211241

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Berat 5g 25g

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Ethyl (S)-4-Chloro-3-hydroxybutyrate is a chiral compound widely used in asymmetric synthesis for the construction of complex molecular structures. This compound plays a vital role in the development of pharmaceuticals and bioactive molecules due to its stereochemical properties. Its ability to participate in various synthetic reactions, such as SN2 and conjugate additions, makes it a valuable building block in organic chemistry. The compound is commonly used in research settings for the synthesis of new compounds with specific biological activities. Its chiral nature allows for precise control over the stereochemistry of the final product, which is crucial in drug development and advanced chemical research. This product is ideal for laboratories focusing on asymmetric synthesis and the creation of bioactive compounds.