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Structure of 132201-32-2
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This chiral amino acid derivative features a phenyl-substituted side chain and exists as the (2R,3S) stereoisomer. The hydrochloride salt enhances solubility and stability, enabling reliable use in peptide synthesis and medicinal chemistry applications under standard conditions.
(2R,3S)-3-Phenylisoserine hydrochloride serves as a stereochemically defined building block for peptide synthesis and chiral auxiliaries. Its phenyl-substituted side chain enables incorporation into bioactive peptidomimetics, while the hydrochloride salt enhances bench stability and simplifies purification. The compound reacts predictably in standard amide coupling protocols and functions effectively in solid-phase and solution-phase synthesis 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: