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Structure of 885518-49-0
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Methyl 6-bromo-1H-indazole-4-carboxylate features a brominated indazole core with a methyl ester at the C4 position, enabling direct functionalization in cross-coupling and derivatization workflows. The electron-deficient heterocycle pairs well with palladium catalysts, while the bench-stable ester group facilitates handling and purification under standard conditions.
Methyl 6-bromo-1H-indazole-4-carboxylate serves as a versatile building block for the synthesis of indazole-based pharmaceuticals and agrochemicals. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports subsequent transformations including hydrolysis, reduction, and amidation. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for iterative synthetic sequences in medicinal chemistry and process development workflows.
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Lot numbers can be found on the outside label of a product: