3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine, identified by CAS 1383625-22-6, is a sophisticated organic intermediate. It features a pyridine core substituted with a trifluoromethyl group at position 2 and a pinacol boronic ester at position 3. The trifluoromethyl group imparts unique electronic properties, while the pinacol boronic ester is a highly stable and reactive moiety commonly employed in Suzuki-Miyaura cross-coupling reactions. This compound's structure makes it a valuable building block for introducing both trifluoromethylated pyridine scaffolds and boronic acid functionalities into complex molecules during research and development.

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