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Structure of 896460-76-7
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This reagent features a reactive dioxopyrrolidinyl carbonate group paired with a pyridin-2-yldisulfanylethyl linker, enabling efficient conjugation through disulfide bond formation. The system facilitates site-specific bioconjugation under mild conditions, leveraging the redox-responsive nature of the disulfide moiety for controlled release or stabilization in biological environments.
2,5-Dioxopyrrolidin-1-yl (2-(pyridin-2-yldisulfanyl)ethyl) carbonate serves as a versatile sulfenylating agent in synthetic chemistry, enabling selective C–S bond formation under mild conditions. The pyridin-2-yl disulfide moiety facilitates controlled release of reactive sulfur species, while the N-hydroxypyrrolidinone leaving group ensures efficient coupling. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for peptide conjugation, thiol labeling, and heterocycle synthesis in medicinal chemistry workflows.
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Lot numbers can be found on the outside label of a product: