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Structure of 1795451-70-5
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Imino(methyl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-l6-sulfanone features a boronate ester group enabling reliable Suzuki-Miyaura coupling under mild conditions. The sulfanone moiety imparts enhanced stability and facilitates efficient incorporation into complex molecular architectures. This reagent streamlines access to functionalized biaryl scaffolds in medicinal chemistry and materials synthesis.
Imino(methyl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)sulfanone serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The stable diborane moiety enables efficient C–C bond formation under mild conditions, while the sulfanone group provides orthogonal reactivity and enhanced functional group tolerance. This compound facilitates rapid access to biaryl scaffolds and heterocyclic frameworks common in medicinal chemistry and materials science, with excellent bench stability and straightforward purification.
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Lot numbers can be found on the outside label of a product: