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Structure of 255060-27-6
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This chiral amino alcohol hydrochloride features a rigid, well-defined stereochemistry at the 1- and 2-positions, enabling precise control in asymmetric synthesis. The phenyl group imparts stability and enhances π-interaction potential, while the protonated amine ensures solubility and facilitates salt formation. Ideal for catalytic applications requiring defined spatial orientation and robust handling under standard conditions.
(1R,2R)-1-Amino-1-phenylpropan-2-ol hydrochloride serves as a chiral building block for β-amino alcohol scaffolds, enabling stereoselective synthesis of pharmaceutical intermediates. Its bench-stable hydrochloride salt form facilitates handling and purification, while the pendant primary amine and secondary alcohol enable orthogonal functionalization. This compound functions as a key synthon in asymmetric synthesis, particularly for accessing bioactive heterocycles and peptidomimetics via established coupling and cyclization protocols.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: