1-Pyrrolidineacetic acid, 4-hydroxy-2-oxo-, (4S)-|99437-11-3,AngeneChemical

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1-Pyrrolidineacetic acid, 4-hydroxy-2-oxo-, (4S)-

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Chemical Name:	1-Pyrrolidineacetic acid, 4-hydroxy-2-oxo-, (4S)-
CAS Number:	99437-11-3
Product Number:	AG005SBJ(AGN-PC-0OP5DC)
Synonyms:
MDL No:
Molecular Formula:	C6H9NO4
Molecular Weight:	159.1400

Identification/Properties
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Identification/Properties

Properties

BP:

465.6°C at 760 mmHg

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

N/A

Hazard Statements:

H315-H319-H335

Precautionary Statements:

P261-P305+P351+P338

Class:

N/A

Packing Group:

N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure

(S)-2-(4-Hydroxy-2-oxopyrrolidin-1-yl)acetic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. It serves as a key chiral building block in the development of pharmaceuticals, agrochemicals, and fine chemicals due to its unique stereochemical properties.One of the primary applications of (S)-2-(4-Hydroxy-2-oxopyrrolidin-1-yl)acetic acid in chemical synthesis is as a chiral auxiliary in asymmetric synthesis. By utilizing its chiral nature, this compound can facilitate the formation of enantiomerically pure compounds, crucial in the pharmaceutical industry where the specific stereochemistry of a molecule can significantly impact its biological activity and safety profile.Moreover, (S)-2-(4-Hydroxy-2-oxopyrrolidin-1-yl)acetic acid can also be employed in the preparation of complex natural products and biologically active molecules. Its ability to induce chirality and control the stereochemistry of reactions makes it a valuable tool for synthesizing structurally diverse compounds with high levels of enantiomeric purity.In summary, (S)-2-(4-Hydroxy-2-oxopyrrolidin-1-yl)acetic acid plays a crucial role in chemical synthesis by enabling the efficient and selective construction of enantiomerically enriched molecules with applications spanning across various industries.