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59554-14-2

3-AMINO-2-HYDROXY-4-PHENYLBUTYRIC ACID

Catalog#: AR00EBE2  |   CAS#: 59554-14-2  |   MDL#: MFCD00070368  |   MF: C10H13NO3  |   MW: 195.2151

Packsize Purity Price Availability Quantity
250mg 98% $5.00 Global Stock Buy Now Add To Cart
1g 98% $9.00 Global Stock Buy Now Add To Cart
5g 98% $32.00 Global Stock Buy Now Add To Cart
100g 98% $552.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EBE2
Chemical Name 3-AMINO-2-HYDROXY-4-PHENYLBUTYRIC ACID
CAS Number 59554-14-2
Molecular Formula C10H13NO3
Molecular Weight 195.2151
MDL Number MFCD00070368
SMILES N[C@@H]([C@@H](C(=O)O)O)Cc1ccccc1

The (2S,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid, also known as $name$, plays a crucial role in chemical synthesis as a valuable chiral building block. Its unique stereochemistry makes it an indispensable component in the creation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, (2S,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid is widely used as a versatile intermediate for the preparation of diversified compounds. Its chiral nature allows for the introduction of specific stereochemical features into organic molecules, making it a powerful tool in the hands of synthetic chemists. By utilizing (2S,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid as a starting material, researchers can access a wide range of enantiopure compounds with high selectivity and efficiency.Moreover, the presence of both an amino and hydroxy group in (2S,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid offers opportunities for further functionalization and derivatization. These functional groups can be selectively modified or transformed, allowing for the incorporation of additional chemical moieties to tailor the properties of the final products. This versatility makes (2S,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid a valuable asset in the development of complex molecules with specific biological or physical activities.Overall, the application of (2S,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid in chemical synthesis highlights its significance as a key building block for the construction of structurally diverse and stereochemically defined compounds with potential applications across various fields of science and technology.
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