The chemical substance known as (2S,4R)-4-((tert-butoxycarbonyl)amino)pyrrolidine-2-carboxylic acid, with the CAS number 1279034-98-8, is an amino acid derivative characterized by its pyrrolidine ring structure. This compound features a chiral center at the 2 and 4 positions, contributing to its stereochemistry, which is crucial for its biological activity. The tert-butoxycarbonyl (Boc) group serves as a protective group for the amino functionality, making it useful in peptide synthesis and other organic reactions. The carboxylic acid group at the 2-position provides acidic properties, allowing for potential interactions in biological systems. This compound is of interest in medicinal chemistry and drug development due to its structural features that may influence binding affinity and selectivity for biological targets. Its solubility, stability, and reactivity can vary based on environmental conditions, making it essential to consider these factors in practical applications. Overall, this compound exemplifies the complexity and utility of amino acid derivatives in chemical and pharmaceutical research.

(2S,4R)-4-((tert-butoxycarbonyl)aMino)pyrrolidine-2-carboxylic acid

1279034-98-8: The chemical substance known as (2S,4R)-4-((tert-butoxycarbonyl)amino)pyrrolidine-2-carboxylic acid, with the CAS number 1279034-98-8, is an amino acid derivative characterized by its pyrrolidine ring structure. This compound features a chiral center at the 2 and 4 positions, contributing to its stereochemistry, which is crucial for its biological activity. The tert-butoxycarbonyl (Boc) group serves as a protective group for the amino functionality, making it useful in peptide synthesis and other organic reactions. The carboxylic acid group at the 2-position provides acidic properties, allowing for potential interactions in biological systems. This compound is of interest in medicinal chemistry and drug development due to its structural features that may influence binding affinity and selectivity for biological targets. Its solubility, stability, and reactivity can vary based on environmental conditions, making it essential to consider these factors in practical applications. Overall, this compound exemplifies the complexity and utility of amino acid derivatives in chemical and pharmaceutical research.

CAS 1279034-98-8

(2S,4R)-4-((tert-butoxycarbonyl)aMino)pyrrolidine-2-carboxylic acid

L-Proline, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, (4R)-

Ref: IN-DA000XK0

(2S,4R)-4-((tert-Butoxycarbonyl)amino)pyrrolidine-2-carboxylic acid

Ref: 10-F080288