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Structure of 955016-25-8
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This chiral piperidine derivative features a tert-butoxycarbonyl-protected amine and a hydroxyl group at the 4-position, enabling direct incorporation into peptide synthesis. The stereochemistry at C2 and C4 ensures high diastereoselectivity in downstream transformations. Bench-stable and moisture-tolerant, it facilitates efficient access to complex heterocyclic scaffolds in medicinal chemistry.
(2S,4R)-1-(tert-Butoxycarbonyl)-4-hydroxypiperidine-2-carboxylic acid serves as a versatile chiral building block for the synthesis of bioactive heterocycles and peptidomimetics. The protected amine and hydroxyl groups enable orthogonal functionalization, while the piperidine core provides structural rigidity. Its bench-stable nature and compatibility with standard coupling and reduction protocols facilitate efficient access to complex scaffolds in medicinal chemistry 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-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: