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Structure of 1206250-70-5
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2-Bromo-6-chlorothiazolo[4,5-c]pyridine features a fused thiazolopyridine core with orthogonal halogen substituents enabling selective cross-coupling. This electron-deficient heterocycle integrates readily into advanced pharmaceutical scaffolds and serves as a key intermediate in medicinal chemistry campaigns requiring halogen-directed functionalization.
2-Bromo-6-chlorothiazolo[4,5-c]pyridine serves as a versatile heterocyclic building block for the synthesis of pharmaceutical intermediates and functional materials. Its complementary halogenation pattern enables selective cross-coupling reactions, including Suzuki and Buchwald–Hartwig transformations, with high chemoselectivity and excellent functional group tolerance. The molecule exhibits robust bench stability and facilitates efficient purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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Lot numbers can be found on the outside label of a product: