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Structure of 884494-84-2
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Methyl 2-fluoro-4-iodonicotinate is a fluorinated heterocyclic ester featuring complementary halogen handles for cross-coupling. The para-iodo group enables palladium-catalyzed transformations, while the ortho-fluoro substituent facilitates selective functionalization. This bifunctional scaffold integrates readily into complex molecular architectures under standard conditions.
Methyl 2-fluoro-4-iodonicotinate serves as a versatile building block for C–H functionalization and cross-coupling reactions, enabling efficient access to substituted pyridine scaffolds. The fluorine and iodine substituents provide orthogonal reactivity—fluorine facilitates electrophilic substitution or nucleophilic displacement, while the iodine supports palladium-catalyzed coupling. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for medicinal chemistry and process development workflows.
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Lot numbers can be found on the outside label of a product: