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Structure of 1227577-02-7
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4-Bromo-2-fluoro-5-methylpyridine features a strategically positioned bromo and fluoro substituent on a methylated pyridine core, enabling selective cross-coupling reactions. The electron-deficient ring facilitates palladium-catalyzed transformations, while the methyl group enhances solubility and steric profile. This scaffold serves as a key intermediate in medicinal chemistry for kinase inhibitors and agrochemicals.
4-Bromo-2-fluoro-5-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 methyl groups provide orthogonal functional handles for further derivatization, while the pyridine core offers stability and favorable electronic properties for target-oriented synthesis. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient assembly of complex heterocyclic scaffolds.
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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: