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Structure of 74536-29-1
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(S)-2-Amino-3-((tert-butoxycarbonyl)amino)propanoic acid is a chiral building block featuring a protected α-amino group and a stereodefined (S)-configuration. This bench-stable derivative enables direct incorporation into peptide synthesis workflows, where the tert-butyl carbamate moiety provides orthogonal protection for amine functionalities during sequential coupling steps.
(S)-2-Amino-3-((tert-butoxycarbonyl)amino)propanoic acid serves as a key chiral building block in peptide synthesis, offering high enantiomeric purity and stability under standard reaction conditions. The Boc-protected amine enables straightforward coupling protocols, while the carboxylic acid facilitates efficient activation and amide bond formation. Its bench-stable nature and compatibility with diverse protecting group strategies make it ideal for iterative solid-phase and solution-phase peptide assembly.
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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: