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Structure of 1232431-48-9
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5-Bromo-2-methoxypyridin-4-amine features a pyridine core functionalized with bromo, methoxy, and amino groups at strategic positions. This trifunctional scaffold enables direct coupling in cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive heterocycles. The electron-rich pyridine ring enhances reactivity in palladium-catalyzed transformations.
5-Bromo-2-methoxypyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine handle. The methoxy group enhances solubility and modulates electronic properties, while the pyridin-4-amine functionality provides a robust site for further derivatization. This compound exhibits excellent bench stability and facilitates efficient purification, making it ideal for iterative synthesis campaigns targeting heterocyclic scaffolds and API intermediates.
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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: