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*For research and further manufacturing use only, not for direct human use.
Structure of 7622-22-2
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(R)-Benzyl 2-hydroxy-3-phenylpropanoate features a chiral benzylic alcohol center flanked by a phenyl ring and ester functionality, enabling stereocontrolled synthesis in natural product and pharmaceutical contexts. This bench-stable derivative integrates readily into asymmetric transformations and serves as a key intermediate in the construction of complex bioactive scaffolds.
(R)-Benzyl 2-hydroxy-3-phenylpropanoate serves as a stereochemically defined chiral building block for the synthesis of bioactive molecules, enabling efficient access to phenylpropanoid scaffolds. Its hydroxyl and ester functionalities support diverse transformations, including oxidation, reduction, and coupling reactions, with excellent bench stability and straightforward purification.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: