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Structure of 88466-74-4
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(S)-1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acid features a chiral piperidine core with a benzyl-protected carboxylic acid at the 3-position, enabling selective functionalization in peptide synthesis. This configuration delivers enhanced stereocontrol during coupling reactions, while the benzyloxy carbonyl group provides stability under standard bench conditions and facilitates orthogonal deprotection via hydrogenolysis.
(S)-1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acid serves as a versatile chiral building block for the synthesis of bioactive heterocycles and peptide-like scaffolds. Its benzyl carbamate protection offers excellent bench stability and compatibility with standard coupling protocols, enabling efficient functionalization at the piperidine nitrogen. The carboxylic acid moiety facilitates direct amidation or esterification, supporting modular assembly of complex molecular architectures 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: