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Structure of 321744-26-7
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This chiral building block features a Boc-protected piperidine core with a hydroxyl-bearing side chain, enabling direct incorporation into complex scaffolds. The methyl ester group facilitates selective derivatization, while the (2R,4S) stereochemistry ensures precise spatial control in asymmetric synthesis. Designed for robust handling and compatibility with standard peptide coupling protocols.
(2R,4S)-N-Boc-4-hydroxypiperidine-2-carboxylic acid methyl ester serves as a versatile chiral building block for the synthesis of bioactive heterocycles and peptidomimetics. The Boc group provides orthogonal protection for the nitrogen, while the hydroxyl and ester functionalities enable selective transformations. Its stability under standard reaction conditions facilitates efficient functionalization, making it well-suited for medicinal chemistry campaigns requiring stereocontrolled access to piperidine-based scaffolds.
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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: