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Structure of 1256807-52-9
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2-Bromo-6-methoxy-4-methylpyridine features a strategically positioned bromine atom enabling direct functionalization in cross-coupling reactions. The methoxy and methyl groups enhance electron density at the pyridine ring, improving reactivity while maintaining stability under standard conditions. This scaffold serves as a key building block for pharmaceutical intermediates and functionalized heterocycles.
2-Bromo-6-methoxy-4-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined regiochemistry and stability under standard reaction conditions. The bromo group facilitates efficient C–C bond formation, while the methoxy and methyl substituents provide predictable electronic modulation and steric control. This compound functions reliably in the synthesis of functionalized pyridine scaffolds commonly found in pharmaceutical 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: