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Structure of 50720-12-2
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3-Bromo-5-methoxypyridine features a pyridine core functionalized with a bromine atom at the 3-position and a methoxy group at the 5-position, enabling selective cross-coupling reactions. This electron-deficient heterocycle integrates readily into pharmaceutical intermediates and advanced materials, offering enhanced reactivity in palladium-catalyzed transformations under standard conditions.
3-Bromo-5-methoxypyridine serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Stille couplings. The bromine and methoxy groups provide orthogonal functionalization sites, while the pyridine core offers enhanced stability and predictable reactivity under standard conditions. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient synthesis of complex heterocyclic scaffolds and functionalized aryl derivatives.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: