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Structure of 28697-09-8
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This chiral piperidine derivative features a benzyl-protected carboxylic acid group, enabling straightforward deprotection and functionalization. The (R)-configuration ensures stereochemical fidelity in asymmetric synthesis, while the benzyloxycarbonyl moiety provides stability and compatibility with standard peptide coupling protocols.
(R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and peptidomimetics. Its bench-stable Boc-like protecting group facilitates orthogonal deprotection strategies, while the piperidine core supports diverse functionalization. The molecule exhibits excellent compatibility with standard coupling reactions and is well-suited for iterative synthesis workflows in API development.
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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: