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Structure of 314741-39-4
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This chiral piperazine derivative features a Boc-protected amine and methyl ester functionality, enabling straightforward deprotection and coupling in peptide and small-molecule synthesis. The (S)-stereochemistry ensures high enantioselectivity in downstream applications.
(S)-1-N-Boc-piperazine-3-carboxylic acid methyl ester serves as a versatile chiral building block in medicinal chemistry, enabling the construction of piperazine-containing scaffolds via standard deprotection and coupling protocols. The Boc group ensures bench stability and orthogonal handling, while the methyl ester facilitates selective transformations. Its defined stereochemistry supports consistent incorporation into bioactive molecules, particularly in kinase inhibitors and CNS-targeted compounds.
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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: