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Structure of 15862-50-7
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3-Bromo-2-methoxy-5-nitropyridine features a pyridine core functionalized with bromo, methoxy, and nitro groups at distinct positions, enabling selective cross-coupling and derivatization. The electron-deficient ring facilitates palladium-catalyzed reactions, while the methoxy group enhances solubility and modulates reactivity. This compound serves as a key intermediate in medicinal chemistry and agrochemical synthesis.
3-Bromo-2-methoxy-5-nitropyridine serves as a versatile building block for the synthesis of functionalized pyridine derivatives. The bromo group enables palladium-catalyzed cross-coupling reactions, while the methoxy and nitro substituents provide orthogonal reactivity for further derivatization. Its stability under standard reaction conditions and compatibility with diverse coupling protocols make it a practical choice for medicinal chemistry and materials science applications.
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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: