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Structure of 110919-71-6
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2-Amino-5-fluoro-6-methylpyridine features a pyridine core functionalized with amino, fluoro, and methyl groups at positions 2, 5, and 6, respectively. This electron-deficient heterocycle integrates readily into pharmaceutical scaffolds, offering enhanced metabolic stability and tunable solubility under standard conditions.
2-Amino-5-fluoro-6-methylpyridine serves as a versatile building block in medicinal chemistry, enabling efficient access to functionalized pyridine scaffolds. Its amino and fluorine substituents offer orthogonal reactivity for late-stage diversification, while the methyl group enhances metabolic stability. The compound exhibits excellent bench stability and compatibility with standard coupling reactions, facilitating streamlined synthesis of bioactive heterocycles.
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Lot numbers can be found on the outside label of a product: