CAS 132622-77-6

1,2-Pyrrolidinedicarboxylic acid, 4-azido-, 1-(1,1-dimethylethyl) ester,(2R,4S)-

Description:

1,2-Pyrrolidinedicarboxylic acid, 4-azido-, 1-(1,1-dimethylethyl) ester, with the CAS number 132622-77-6, is a chemical compound characterized by its unique structural features, including a pyrrolidine ring and azido functional group. This compound is an ester derivative, which typically indicates it has potential applications in organic synthesis and medicinal chemistry. The presence of the azido group suggests that it may participate in click chemistry reactions, making it valuable for bioconjugation and material science applications. The specific stereochemistry, indicated by the (2R,4S) configuration, implies that the compound has chiral centers, which can influence its biological activity and interaction with other molecules. Additionally, the tert-butyl ester group contributes to its lipophilicity, potentially affecting its solubility and permeability in biological systems. Overall, this compound's unique combination of functional groups and stereochemistry makes it a subject of interest in various fields, including pharmaceuticals and chemical research.

Formula: C₁₀H₁₆N₄O₄

(2R,4S)-Boc-D-Pro(4-N3)-OH

CAS: 132622-77-6

(2R,4S)-Boc-D-Pro(4-N3)-OH is a click chemistry reagent possessing an azide group. This compound is capable of undergoing copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing alkyne groups. Additionally, it can participate in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with compounds that have DBCO or BCN groups.

Formula: C₁₀H₁₆N₄O₄

Color and Shape: Solid

Molecular weight: 256.26

Ref: TM-T89667