The chemical substance known as {(3S)-3-[(tert-butoxycarbonyl)amino]-2-oxopyrrolidin-1-yl}acetic acid, with the CAS number 79839-26-2, is a derivative of pyrrolidine, which is a five-membered nitrogen-containing heterocycle. This compound features a chiral center, indicated by the (3S) configuration, which contributes to its stereochemical properties. The presence of the tert-butoxycarbonyl (Boc) group suggests that it is likely used as a protecting group in peptide synthesis, allowing for selective reactions without interfering with the amino functionality. The acetic acid moiety indicates that it possesses acidic characteristics, which may influence its solubility and reactivity in various environments. The compound is typically utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its structural features suggest potential applications in drug design, where the balance of hydrophilicity and lipophilicity is crucial for bioactivity. Overall, this compound exemplifies the complexity and utility of amino acid derivatives in chemical research and development.

{(3S)-3-[(tert-butoxycarbonyl)amino]-2-oxopyrrolidin-1-yl}acetic acid

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(S)-(3-N-Boc-Amino-2-oxo-pyrrolidin-1-yl)-acetic acid

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CAS 79839-26-2: {(3S)-3-[(tert-butoxycarbonyl)amino]-2-oxopyrrolidin-1-yl}acetic acid

(S)-(3-N-Boc-Amino-2-oxo-pyrrolidin-1-yl)-acetic acid

Ref: 10-F040988

Boc-(S)-3-amino-2-oxo-1-pyrrolidine-acetic acid

Ref: 3D-FB49517

(S)-2-(3-((tert-Butoxycarbonyl)amino)-2-oxopyrrolidin-1-yl)acetic acid

Ref: IN-DA00564N