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Structure of 1211517-76-8
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3-Bromo-5-fluoro-4-methylpyridine features a pyridine core with strategically positioned halogen and methyl groups, enabling selective cross-coupling reactions. The electron-deficient ring facilitates palladium-catalyzed transformations, while the ortho-bromine serves as a high-reactivity handle for C–C bond formation under mild conditions. This bench-stable building block supports efficient synthesis of functionalized heterocycles in medicinal chemistry and materials science.
3-Bromo-5-fluoro-4-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen and electron-withdrawing fluorine substituents. The methyl group provides a handle for further functionalization, while the pyridine core offers robust stability and predictable reactivity in standard synthetic workflows.
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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: