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Structure of 848482-93-9
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This bench-stable, moisture-tolerant piperazine derivative features a protected amine and carboxylic acid functionality, enabling straightforward incorporation into peptide and macrocyclic scaffolds. The tert-butoxycarbonyl group facilitates selective deprotection under mild acidic conditions, while the electron-rich piperazine core supports efficient conjugation chemistry in synthetic medicinal chemistry workflows.
(S)-4-(tert-Butoxycarbonyl)piperazine-2-carboxylic acid serves as a versatile chiral building block for the synthesis of piperazine-based pharmaceutical intermediates. The Boc-protected amine and carboxylic acid functionalities enable orthogonal derivatization, facilitating peptide coupling, reductive amination, and cyclization reactions. Its bench-stable nature and compatibility with standard purification methods support efficient scale-up in medicinal chemistry campaigns.
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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: