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Structure of 1227574-33-5
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2-Bromo-4-methoxy-5-methylpyridine features a pyridine core functionalized with bromo, methoxy, and methyl groups at positions 2, 4, and 5 respectively. This electron-deficient heterocycle enables efficient cross-coupling reactions, serving as a key building block in pharmaceutical synthesis and materials chemistry. The methoxy and methyl substituents enhance solubility and modulate reactivity, while the bromine handles facilitate palladium-catalyzed transformations under standard conditions.
2-Bromo-4-methoxy-5-methylpyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic bromide site. The methoxy and methyl groups provide orthogonal functional handles for further derivatization, while the pyridine core offers favorable electronic properties for coupling with aryl, vinyl, and alkyl boranes or stannanes. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to substituted pyridine scaffolds relevant to medicinal chemistry and agrochemical 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: