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Structure of 39747-65-4
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This (S)-configured reagent features a pyrrolidinone-activated ester coupled with a protected amino acid side chain, enabling efficient coupling in peptide synthesis. The tert-butoxycarbonyl group provides stability and orthogonal deprotection compatibility. This scaffold facilitates selective amide bond formation under mild conditions, streamlining the assembly of complex peptide sequences.
(S)-2,5-Dioxopyrrolidin-1-yl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate serves as a robust activated ester for the selective coupling of hydroxyl and amine functionalities. Its (S)-configured backbone enables stereocontrolled synthesis of β-hydroxy-α-amino acid derivatives, commonly used in peptide macrocyclization and peptidomimetic construction. The tert-butyl carbamate group provides orthogonal protection, while the pyrrolidinone ester moiety ensures efficient reactivity under mild conditions, facilitating purification and compatibility with sensitive substrates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: