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Structure of 134441-61-5
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(R)-1-Boc-2-piperidinemethanol features a stereochemically defined piperidine core with a robust Boc-protected amine and hydroxymethyl group. This configuration enables direct incorporation into chiral scaffolds for medicinal chemistry, offering enhanced solubility and stability under standard conditions. The protected amine facilitates sequential functionalization without racemization.
(R)-1-Boc-2-piperidinemethanol serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to piperidine-containing scaffolds. The Boc-protected amine and pendant hydroxyl group offer orthogonal functionalization potential, facilitating downstream modifications via standard coupling, reduction, or derivatization protocols. Its bench-stable solid form and compatibility with common reaction conditions make it well-suited for multi-step synthesis and scale-up applications.
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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: