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Structure of 850882-87-0
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6-Bromo-3-methoxy-2-methylpyridine features a strategically positioned bromine atom at the 6-position, enabling direct functionalization in cross-coupling reactions. The methoxy group at C3 and methyl substituent at C2 enhance electronic modulation and solubility, while maintaining bench-stable handling under standard conditions.
6-Bromo-3-methoxy-2-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromine substituent. The methoxy and methyl groups provide orthogonal functional handles for further derivatization, while the pyridine core offers favorable electronic properties for heterocyclic scaffold elaboration. Bench-stable and readily purified by column chromatography, it functions efficiently in standard coupling protocols and supports modular synthesis of complex nitrogen-containing architectures.
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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: