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Structure of 1211537-29-9
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2-Bromo-4-fluoro-5-methylpyridine features a strategically positioned bromine and fluorine 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 compound serves as a key intermediate in medicinal chemistry for constructing bioactive heterocycles under standard conditions.
2-Bromo-4-fluoro-5-methylpyridine serves as a versatile building block in medicinal chemistry, enabling late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its orthogonal halogenation pattern facilitates selective derivatization at the bromo position while preserving the fluorine and methyl groups. The compound exhibits good bench stability and compatibility with standard reaction conditions, making it suitable for constructing diverse heterocyclic scaffolds and API intermediates.
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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: