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Structure of 180608-37-1
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2-Bromo-6-fluoro-4-methylpyridine features a strategically positioned bromine and fluorine substitution on a pyridine core, enabling selective cross-coupling reactions. The methyl group enhances electron density at C4, while the ortho-fluorine improves metabolic stability. This compound serves as a key intermediate in medicinal chemistry for constructing bioactive heterocycles under standard conditions.
2-Bromo-6-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 bromine site facilitates Suzuki, Negishi, and Buchwald–Hartwig couplings, while the fluorine and methyl groups provide orthogonal functionalization potential. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for constructing complex heterocyclic scaffolds in API 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: