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Structure of 1030377-21-9
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(S)-1-Boc-2-Hydroxymethyl-piperazine features a chiral piperazine core with a Boc-protected amine and a hydroxymethyl group, enabling selective functionalization in asymmetric synthesis. The pendant hydroxyl group offers versatility for derivatization, while the Boc handle ensures stability during multi-step transformations. This scaffold integrates readily into bioactive molecule design, particularly in kinase inhibitor and peptide mimic development.
(S)-1-Boc-2-Hydroxymethyl-piperazine serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of piperazine-based scaffolds with defined stereochemistry. The Boc group provides stable protection of the primary amine, while the hydroxymethyl functionality offers a handle for further derivatization via oxidation, substitution, or coupling reactions. Its bench-stable nature and compatibility with standard peptide and heterocyclic synthesis protocols make it well-suited for iterative library construction and 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: