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Structure of 33209-01-7
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This chiral amino acid derivative features a (2S,3R) stereochemistry critical for biological activity. The hydroxyl and amide functionalities enable hydrogen bonding in peptide mimetics, while the hydrochloride salt ensures stability and solubility under standard conditions.
(2S,3R)-2-Amino-3-hydroxybutanamide hydrochloride serves as a stereochemically defined building block for the synthesis of β-amino alcohol motifs prevalent in bioactive molecules. Its amine and hydroxyl functionalities enable straightforward derivatization, including acylation and etherification, while the hydrochloride salt ensures excellent bench stability and ease of handling. This compound functions effectively in peptide-like scaffold construction and is compatible with standard protecting group strategies in medicinal chemistry workflows.
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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: