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Structure of 2304754-47-8
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This triflate ester enables efficient C–C bond formation via palladium-catalyzed coupling, featuring a methoxy-substituted benzyl group that enhances solubility and stability. The piperidinone scaffold provides a rigid, electron-deficient platform for selective functionalization in complex molecule synthesis.
1-(4-Methoxybenzyl)-2,6-dioxopiperidin-3-yl trifluoromethanesulfonate serves as a versatile acylating agent in peptide and heterocycle synthesis, enabling efficient C–H functionalization and amide bond formation. Its triflate leaving group facilitates nucleophilic substitution under mild conditions, while the 4-methoxybenzyl protecting group ensures stability and ease of removal. Ideal for bench-scale applications requiring high reactivity and predictable transformation pathways.
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Lot numbers can be found on the outside label of a product: