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Structure of 88784-91-2
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This chiral amino alcohol hydrochloride delivers a stereochemically defined scaffold for asymmetric synthesis and medicinal chemistry. The (1R,2S) configuration ensures predictable reactivity in catalytic transformations, while the phenyl group enhances structural rigidity and solubility in polar solvents. Bench-stable under standard conditions, it integrates seamlessly into peptide mimetics and bioactive molecule design.
(1R,2S)-1-Amino-1-phenylpropan-2-ol hydrochloride serves as a chiral building block for the synthesis of β-amino alcohols and pharmaceutically relevant heterocycles. Its well-defined stereochemistry enables stereoselective transformations in medicinal chemistry workflows. The hydrochloride salt enhances bench stability and simplifies handling and purification, while maintaining compatibility with common coupling and functionalization reactions.
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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: