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Structure of 1034658-69-9
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tert-Butyl (2-fluoro-4-iodopyridin-3-yl)carbamate delivers a fluorinated, iodinated pyridine scaffold with enhanced stability and solubility. This bench-stable building block integrates readily into cross-coupling reactions, enabling efficient access to complex heterocyclic architectures in medicinal chemistry and materials science.
tert-Butyl (2-fluoro-4-iodopyridin-3-yl)carbamate serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable iodine handle. The molecule features orthogonal functional groups—fluorine for electrophilic substitution and the Boc-protected amine for selective derivatization—facilitating modular synthesis of complex pyridine-based scaffolds. Its bench stability and ease of purification make it well-suited for high-throughput screening and process-scale applications.
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Lot numbers can be found on the outside label of a product: