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Structure of 91574-33-3
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This pyrrolidinone ester features a reactive acylating group flanked by a para-substituted phenyl ring, enabling efficient coupling in peptide and biomolecule synthesis. The dioxopyrrolidinyl moiety delivers high electrophilicity and stability under standard conditions, facilitating clean activation without significant hydrolysis.
2,5-Dioxopyrrolidin-1-yl 2-(4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)phenyl)acetate serves as a robust activated ester for amide bond formation, enabling efficient coupling with primary amines under mild conditions. The pyrrole-containing aryl acetic acid scaffold provides enhanced solubility and stability in organic media, facilitating purification and scalability. Functions reliably in peptide synthesis and conjugation workflows where orthogonality and reaction efficiency are critical.
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Lot numbers can be found on the outside label of a product: