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Structure of 448906-60-3
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(4-Bromo-6-methylpyridin-2-yl)methanol features a brominated pyridine core with a methyl group at the 6-position and a reactive hydroxymethyl functionality. This bench-stable, moisture-tolerant reagent integrates readily into cross-coupling workflows and serves as a key intermediate in the synthesis of bioactive heterocycles and functionalized pharmaceutical scaffolds.
(4-Bromo-6-methylpyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via its bromo and hydroxymethyl groups. The bromine facilitates Suzuki-Miyaura and Stille couplings, while the alcohol functions as a handle for derivatization or protection. Its bench-stable nature and compatibility with diverse reaction conditions make it suitable for modular synthesis of pyridine-based scaffolds in drug discovery workflows.
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Lot numbers can be found on the outside label of a product: