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Structure of 30189-36-7
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This chiral dipeptide derivative features a (S)-configured pyrrolidinone core paired with two tert-butoxycarbonyl-protected amino groups, enabling selective coupling in peptide synthesis. The orthogonal protection facilitates sequential elongation while maintaining stereochemical integrity under standard conditions.
(S)-2,5-Dioxopyrrolidin-1-yl 2,6-bis((tert-butoxycarbonyl)amino)hexanoate serves as a versatile dipeptide coupling reagent, enabling efficient amide bond formation under mild conditions. The molecule features two orthogonal tert-butyl carbamate-protected amino groups flanking a central aliphatic chain, facilitating sequential peptide elongation. Its pyrrolidinone ester moiety ensures high reactivity with nucleophiles while maintaining bench stability and ease of purification. Functions reliably in solid-phase and solution-phase peptide synthesis, particularly for constructing complex oligopeptides and cyclic scaffolds.
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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: