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Structure of 1211521-17-3
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1-(5-Bromo-3-methoxypyridin-2-yl)ethan-1-one features a brominated pyridine core with a methoxy substituent at C3 and a ketone at C2, enabling direct incorporation into cross-coupling reactions. The electron-deficient aryl bromide facilitates palladium-catalyzed transformations, while the acetyl group provides a handle for further functionalization. This compound serves as a key intermediate in medicinal chemistry and materials synthesis.
1-(5-Bromo-3-methoxypyridin-2-yl)ethan-1-one serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromo group facilitates Suzuki, Stille, and Negishi couplings, while the acetyl functionality provides a handle for further derivatization. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for modular synthesis of bioactive heterocycles and pharmaceutical intermediates.
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Lot numbers can be found on the outside label of a product: