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Structure of 170235-18-4
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Methyl 6-bromo-5-methoxypicolinate is a bench-stable, electron-deficient pyridine derivative featuring a bromine at the 6-position and a methoxy group at the 5-position. This configuration enables selective cross-coupling reactions in late-stage functionalization, particularly under palladium catalysis. The ester moiety facilitates derivatization and incorporation into complex molecular architectures.
Methyl 6-bromo-5-methoxypicolinate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions at the C6 bromine site. The methoxy group at C5 provides electronic modulation and enhances solubility, while the methyl ester facilitates downstream transformations. This compound exhibits excellent bench stability and is compatible with standard reaction conditions, making it ideal for constructing complex pyridine-based scaffolds in medicinal chemistry and materials science applications.
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Lot numbers can be found on the outside label of a product: