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Structure of 741709-67-1
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This boronate-functionalized pyridine integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, delivering trifluoromethyl-substituted biaryls with high efficiency. The tetramethylborolane moiety ensures excellent stability and ease of handling, while the chloropyridine framework enables selective cross-coupling.
2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)pyridine serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the boronate ester enables efficient coupling with aryl and heteroaryl halides under mild conditions. Bench-stable and compatible with diverse functional groups, it facilitates rapid access to complex pyridine-based scaffolds relevant to medicinal chemistry and materials science.
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Lot numbers can be found on the outside label of a product: