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Structure of 17126-67-9
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(R)-3-Hydroxy-2-phenylpropanoic acid features a chiral center at the C3 position, delivering high enantioselectivity in asymmetric synthesis. The hydroxyl group enables derivatization for bioactive molecule construction, while the aromatic phenyl moiety imparts stability and enhanced solubility in organic media. This configuration supports efficient incorporation into complex scaffolds under standard bench conditions.
(R)-3-Hydroxy-2-phenylpropanoic acid serves as a key chiral building block for synthesizing bioactive molecules and pharmaceutical intermediates. Its well-defined stereochemistry enables reliable asymmetric transformations, while the hydroxyl and carboxylic acid functionalities support diverse functional group interconversions. The compound exhibits good bench stability and facilitates efficient derivatization in standard organic 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: