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Structure of 724787-52-4
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Benzyl trans-4-((tert-butoxycarbonyl)amino)-3-hydroxypiperidine-1-carboxylate features a sterically hindered, bench-stable piperidine core with orthogonal functional handles: a protected amine and a reactive hydroxyl group. This configuration enables selective derivatization in complex molecule synthesis.
Benzyl trans-4-((tert-butoxycarbonyl)amino)-3-hydroxypiperidine-1-carboxylate serves as a key chiral building block for the synthesis of piperidine-based pharmaceutical intermediates. The trans-configured hydroxypiperidine core, combined with orthogonal Boc and benzyl protecting groups, enables selective functionalization and efficient deprotection sequences. Its bench-stable nature and compatibility with standard coupling reactions facilitate streamlined access to complex heterocyclic scaffolds in medicinal chemistry campaigns.
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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: