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62182-54-1

1,2-Pyrrolidinedicarboxylic acid, 3-hydroxy-, 1-(phenylmethyl) ester,(2S-trans)-

Catalog#: AR00ELRR  |   CAS#: 62182-54-1  |   MDL#: MFCD29917045  |   MF: C13H15NO5  |   MW: 265.2619

Packsize Purity Price Availability Quantity
100mg 97% $181.00 Global Stock Buy Now Add To Cart
250mg 97% $288.00 Global Stock Buy Now Add To Cart
500mg 97% $480.00 Global Stock Buy Now Add To Cart
1g 97% $720.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00ELRR
Chemical Name 1,2-Pyrrolidinedicarboxylic acid, 3-hydroxy-, 1-(phenylmethyl) ester,(2S-trans)-
CAS Number 62182-54-1
Molecular Formula C13H15NO5
Molecular Weight 265.2619
MDL Number MFCD29917045
SMILES O[C@H]1CCN([C@@H]1C(=O)O)C(=O)OCc1ccccc1

The (2S,3S)-1-((Benzyloxy)carbonyl)-3-hydroxypyrrolidine-2-carboxylic acid, often referred to as $name$, is a crucial compound in chemical synthesis due to its versatile applications. $name$ plays a vital role as a chiral building block in the synthesis of various pharmaceuticals and complex organic molecules. Its unique stereochemistry and functional groups make it an ideal starting material for the production of chiral molecules with high purity and desired biological activity.In organic synthesis, $name$ can be used as a key intermediate for the preparation of peptide derivatives, amino acids, and other biologically active compounds. Its presence allows for the introduction of specific functional groups at precise positions in the molecule, enabling chemists to fine-tune the properties of the final product.Furthermore, $name$ is utilized in the development of novel drug candidates, as its structural features can be optimized to enhance the pharmacological profile of the resulting molecules. Its use in medicinal chemistry highlights its importance as a valuable tool for drug discovery and development processes.Overall, the application of (2S,3S)-1-((Benzyloxy)carbonyl)-3-hydroxypyrrolidine-2-carboxylic acid in chemical synthesis is instrumental in the construction of complex organic molecules with defined stereochemistry and biological activity.
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