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Structure of 1051316-41-6
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(R)-4-Hydroxypiperidin-2-one is a stereochemically defined heterocyclic scaffold featuring a hydroxyl group at the C4 position and a carbonyl at C2, enabling precise molecular recognition. This configuration imparts enhanced solubility and metabolic stability compared to racemic counterparts, facilitating its integration into bioactive molecules. The compound serves as a key building block in medicinal chemistry for peptidomimetics and kinase inhibitors.
(R)-4-Hydroxypiperidin-2-one serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles through standard amide coupling, reduction, and cyclization reactions. Its well-defined stereochemistry and bench-stable nature facilitate reliable incorporation into complex molecular architectures, including kinase inhibitors and GPCR-targeted therapeutics. The molecule exhibits favorable functional group tolerance and compatibility with common protecting group strategies, making it ideal for iterative synthesis workflows.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H318
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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: