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Structure of 470478-90-1
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tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine-1-carboxylate features a boronate ester group enabling efficient Suzuki-Miyaura coupling. The tert-butyl carbamate protects the piperazine nitrogen, enhancing stability and solubility. This reagent streamlines access to complex biaryl architectures in medicinal chemistry and materials synthesis under standard conditions.
tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine-1-carboxylate serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The piperazine core provides a pharmacophoric scaffold commonly found in medicinal chemistry, while the boronate ester enables efficient C–C bond formation under mild conditions. Bench-stable and compatible with diverse functional groups, it facilitates rapid assembly of complex arylated heterocycles with high reproducibility in both academic and industrial settings.
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Lot numbers can be found on the outside label of a product: