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Structure of 864830-16-0
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5-Bromo-2-fluoro-4-methylpyridine features a trifunctional pyridine core enabling direct incorporation into pharmaceutical scaffolds. The electron-deficient ring pairs with orthogonal halogen handles for late-stage diversification via cross-coupling. This bench-stable, moisture-tolerant reagent streamlines synthesis of kinase inhibitors and bioactive heterocycles under standard conditions.
5-Bromo-2-fluoro-4-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The fluorine and bromine substituents offer orthogonal functionalization potential, while the methyl group enhances solubility and modulates electronic properties. This compound demonstrates excellent bench stability and facilitates efficient synthesis of complex heterocyclic scaffolds relevant to pharmaceutical development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
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Lot numbers can be found on the outside label of a product: