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Structure of 169448-87-7
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(R)-1-Boc-2-Hydroxymethyl-piperazine features a chiral piperazine core with a stable Boc-protected amine and a pendant hydroxymethyl group, enabling selective derivatization. This bench-stable scaffold integrates readily into complex molecular architectures, offering enhanced solubility and functional handle versatility in medicinal chemistry workflows.
(R)-1-Boc-2-hydroxymethylpiperazine serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient access to piperazine-based scaffolds. The Boc group provides stable protection of the primary amine, while the pendant hydroxymethyl functionality allows for further derivatization via oxidation or coupling reactions. Its bench-stable nature and compatibility with standard peptide and heterocyclic coupling protocols make it well-suited for medicinal chemistry and process development workflows.
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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: