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Structure of 368866-11-9
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(S)-1-Boc-4-(aminocarboxymethyl)piperidine is a chiral building block featuring a protected amine and a carboxymethyl group on the piperidine ring. This configuration enables direct incorporation into peptide-like scaffolds and bioactive molecules, offering high stereochemical fidelity. The Boc group ensures stability during synthesis and simplifies deprotection under mild acidic conditions.
(S)-1-Boc-4-(aminocarboxymethyl)piperidine serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient access to piperidine-based scaffolds. The Boc-protected amine and pendant carboxylic acid group offer orthogonal functionalization potential, facilitating sequential derivatization in medicinal chemistry campaigns. Bench-stable and readily purified by standard chromatography, it functions effectively in coupling reactions, reductive amination, and heterocycle formation under mild conditions.
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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: