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Structure of 1033713-11-9
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This chiral piperazine derivative features a protected amine and a ketone-functionalized ring, enabling direct incorporation into peptide conjugates and bioactive molecule scaffolds. The tert-butoxycarbonyl group provides stability during synthesis, while the oxo and carboxylic acid moieties offer versatile handles for further derivatization under standard conditions.
(S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid serves as a versatile chiral building block in the synthesis of piperazine-based scaffolds. Its Boc-protected amine and carboxylic acid functionalities enable sequential derivatization, while the 5-oxo group facilitates nucleophilic addition and ring functionalization. The compound exhibits excellent bench stability and ease of purification, making it well-suited for medicinal chemistry campaigns requiring precise stereocontrol and functional group compatibility.
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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: