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Structure of 106910-77-4
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(R)-2-(Benzylamino)-3-hydroxypropanoic acid features a chiral center at the C-2 position, delivering enantiomerically pure stereochemistry essential for asymmetric synthesis. The pendant hydroxyl group enables selective derivatization, while the benzylamino moiety imparts solubility and facilitates incorporation into peptidomimetic scaffolds. This compound serves as a key building block in the development of bioactive small molecules and enzyme inhibitors.
(R)-2-(Benzylamino)-3-hydroxypropanoic acid serves as a key chiral building block for the synthesis of β-amino alcohol motifs found in bioactive molecules. Its well-defined stereochemistry enables reliable incorporation into peptidomimetics and kinase inhibitors. The molecule exhibits bench stability, tolerates standard protecting group manipulations, and participates in efficient coupling reactions with minimal racemization.
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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: