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Structure of 1313441-88-1
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tert-Butyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate features a boronate handle integrated into a cyclopropyl-substituted aryl scaffold, enabling efficient Suzuki-Miyaura coupling under mild conditions. The tetramethyl-dioxaborolane moiety provides excellent stability and reactivity, while the tert-butyl carbamate group offers convenient protection for amine functionalities during synthesis. This compound serves as a robust building block in medicinal chemistry and complex molecule assembly.
tert-Butyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate serves as a robust boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The cyclopropyl group imparts structural rigidity and metabolic stability, while the tert-butyl carbamate provides excellent bench stability and convenient deprotection under mild acidic conditions. Its compatibility with diverse reaction partners and ease of purification make it ideal for constructing complex biaryl scaffolds in medicinal chemistry and materials synthesis.
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