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Home  > (S)-Ethyl 2-hydroxy-4-phenylbutanoate

AA31216

125639-64-7 | (S)-Ethyl 2-hydroxy-4-phenylbutanoate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $40.00 $28.00 -   +
1g 98% in stock $66.00 $47.00 -   +
5g 98% in stock $169.00 $118.00 -   +
25g 98% in stock $626.00 $439.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA31216
Chemical Name: (S)-Ethyl 2-hydroxy-4-phenylbutanoate
CAS Number: 125639-64-7
Molecular Formula: C12H16O3
Molecular Weight: 208.2536
MDL Number: MFCD03095465
SMILES: CCOC(=O)[C@H](CCc1ccccc1)O

 

Upstream Synthesis Route
  • (S)-4-Phenyl-2-hydroxybutanoic acid ethyl ester is a versatile compound commonly used in chemical synthesis for its chiral properties. As an enantiomerically pure derivative of 4-Phenyl-2-hydroxybutanoic acid, this compound plays a crucial role in asymmetric synthesis.One of the key applications of (S)-4-Phenyl-2-hydroxybutanoic acid ethyl ester is in the production of pharmaceutical intermediates and active pharmaceutical ingredients (APIs). Its chiral nature allows for the creation of optically pure compounds, which are essential in drug development and synthesis.Additionally, this compound is often utilized in the preparation of chiral ligands for catalytic reactions in organic synthesis. Its stereochemistry helps to control and enhance the selectivity and yield of various chemical reactions, making it a valuable building block in the creation of complex molecules.Moreover, (S)-4-Phenyl-2-hydroxybutanoic acid ethyl ester can serve as a precursor for the synthesis of chiral building blocks used in the production of fine chemicals, agrochemicals, and fragrances. Its unique molecular structure opens up possibilities for the creation of diverse chemical compounds with specific chirality requirements.Overall, the application of (S)-4-Phenyl-2-hydroxybutanoic acid ethyl ester in chemical synthesis highlights its importance in enabling the production of enantiomerically pure compounds with tailored properties for various industrial and research purposes.
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