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Structure of 181228-33-1
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(S)-Methyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate hydrochloride features a chiral α-amino acid scaffold with orthogonal protection: the amine is masked as a tert-butoxycarbonyl (Boc) group, while the carboxylic acid is esterified. This configuration enables selective deprotection and coupling in peptide synthesis workflows. The hydrochloride salt enhances solubility and handling stability under standard bench conditions.
(S)-Methyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate hydrochloride serves as a key chiral building block in peptide synthesis and medicinal chemistry. The protected amine and carboxylate functionalities enable orthogonal transformations, while the (S)-configuration ensures stereochemical fidelity in target molecules. Bench-stable and readily purified by crystallization, it facilitates efficient coupling reactions and downstream derivatization in multi-step syntheses.
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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: