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Structure of 132622-69-6
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This chiral pyrrolidine derivative features a protected amino group and carboxylic acid functionality, enabling direct incorporation into peptide synthesis. The (2S,4R) stereochemistry ensures high enantioselectivity in downstream conjugations, while the tert-butoxycarbonyl group provides stability under standard conditions.
(2S,4R)-4-Amino-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid serves as a stereochemically defined building block for the synthesis of pyrrolidine-based peptidomimetics and bioactive heterocycles. The protected amine and carboxylic acid functionalities enable orthogonal derivatization, while the (2S,4R) configuration ensures high diastereoselectivity in downstream transformations. Its bench-stable tert-butyl carbamate group facilitates purification and compatibility with standard coupling protocols, making it well-suited for medicinal chemistry campaigns requiring precise stereocontrol.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: