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Structure of 63088-78-8
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This chiral piperidine derivative features a hydroxyl group at the 5-position and a carboxylic acid at the 2-position, enabling integration into bioactive scaffolds. The stereochemistry at C2 and C5 imparts defined spatial orientation, enhancing target selectivity in medicinal chemistry applications. Bench-stable and moisture-tolerant, it serves as a key building block for peptide mimetics and CNS-targeted compounds.
(2S,5S)-5-Hydroxypiperidine-2-carboxylic acid serves as a stereochemically defined building block for the synthesis of bioactive heterocycles and peptidomimetics. Its constrained piperidine core with orthogonal hydroxyl and carboxylic acid functionalities enables selective derivatization in medicinal chemistry workflows. The compound exhibits excellent bench stability and facilitates efficient incorporation into macrocyclic and linear scaffolds via standard coupling and protection strategies.
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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: