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Structure of 161948-70-5
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(1-Boc-4-piperidinyloxy)acetic acid features a protected piperidinyl ether moiety paired with a carboxylic acid handle, enabling direct conjugation in peptide and small-molecule synthesis. The Boc group ensures stability during handling and storage, while the oxygen-linked piperidine facilitates incorporation into bioactive scaffolds requiring polar, basic nitrogen centers. This derivative supports efficient derivatization under mild conditions without epimerization risk.
(1-Boc-4-piperidinyloxy)acetic acid serves as a stable, bench-ready building block for the synthesis of piperidinyl ether-containing compounds. Its Boc-protected amine and carboxylic acid functionalities enable orthogonal handling in multi-step syntheses. The molecule facilitates efficient incorporation into bioactive scaffolds via standard coupling reactions and supports diverse functionalization at both the piperidine nitrogen and side chain, making it well-suited for medicinal chemistry campaigns requiring precise structural control.
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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: