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Structure of 796096-64-5
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This chiral building block features a Boc-protected piperazine core with a methyl ester-functionalized carboxylic acid, enabling direct incorporation into peptide and small-molecule synthesis. The (S)-stereocenter ensures high enantiomeric purity for asymmetric applications. Designed for stability under standard conditions, it facilitates efficient derivatization in medicinal chemistry workflows.
(S)-1-N-Boc-piperazine-2-carboxylic acid methyl ester serves as a versatile chiral building block for the synthesis of piperazinone-containing scaffolds. Its Boc-protected amine and ester functionalities enable orthogonal transformations, facilitating efficient coupling reactions and selective deprotection sequences. The molecule exhibits excellent bench stability and is compatible with standard peptide coupling protocols, making it well-suited for medicinal chemistry campaigns targeting CNS-active compounds and kinase inhibitors.
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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: