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Structure of 476014-92-3
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(S)-4-Hydroxypiperidin-2-one is a chiral heterocyclic scaffold featuring a hydroxyl group at the C4 position and a carbonyl at C2, enabling direct functionalization in asymmetric synthesis. This bench-stable motif integrates readily into bioactive molecules, offering enhanced solubility and hydrogen-bonding capacity for medicinal chemistry applications.
(S)-4-Hydroxypiperidin-2-one serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to bioactive heterocycles. Its well-defined stereochemistry and functional group tolerance facilitate direct derivatization via alkylation, acylation, or reductive amination. The molecule's bench-stable nature and compatibility with standard purification methods make it ideal for multi-step synthesis workflows targeting peptidomimetics and kinase inhibitors.
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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: