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Structure of 134441-93-3
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1-Boc-(S)-2-piperidinemethanol features a chiral piperidine core with a protected hydroxymethyl group, enabling selective functionalization in asymmetric synthesis. This bench-stable derivative integrates readily into complex molecular architectures, offering reliable access to bioactive piperidine scaffolds under standard conditions.
1-Boc-(S)-2-piperidinemethanol serves as a versatile chiral building block for the synthesis of piperidine-based pharmaceutical intermediates. The Boc-protected amine enables straightforward functionalization and orthogonal deprotection, while the pendant hydroxyl group supports derivatization via esterification or ether formation. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient access to complex heterocyclic scaffolds in medicinal chemistry and process development 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-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: