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Structure of 59554-14-2
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This chiral amino acid derivative features a stereodefined (2S,3R) configuration, combining a primary amine and a β-hydroxyl group flanking a phenyl-substituted carbon chain. The structural motif enables integration into peptide-based scaffolds and bioactive molecules, where the hydroxyamine functionality supports hydrogen bonding and metabolic stability. Its bench-stable nature facilitates handling in synthetic workflows.
(2S,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid serves as a stereochemically defined building block for β-amino alcohol and β-hydroxy amino acid derivatives. Its well-defined stereocenters enable reliable incorporation into peptidomimetics and bioactive heterocycles. The molecule exhibits bench stability, tolerates common functional group manipulations, and facilitates efficient coupling reactions via its carboxylic acid and amine functionalities.
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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: