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Structure of 886372-61-8
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5-Bromo-4-methoxy-2-methylpyridine features a pyridine core functionalized with bromo, methoxy, and methyl groups at strategic positions, enabling selective cross-coupling reactions. The electron-deficient aromatic ring pairs with the ortho-directed methyl group to facilitate regioselective transformations. This bench-stable building block integrates efficiently into pharmaceutical intermediates and agrochemical scaffolds.
5-Bromo-4-methoxy-2-methylpyridine serves as a versatile building block in medicinal chemistry and heterocyclic 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 and stability under standard reaction conditions. Its bench-stable nature and compatibility with common synthetic protocols make it well-suited for modular scaffold construction in API development.
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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: