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Structure of 847799-64-8
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2-Bromo-N-methylpyridin-4-amine features a bromine substituent at the pyridine ring’s 2-position and a methylamino group at the 4-position, enabling direct functionalization in cross-coupling reactions. The electron-deficient pyridine ring enhances reactivity toward palladium-catalyzed transformations, while the N-methyl group improves solubility and stability under standard conditions. This compound serves as a key building block for bioactive heterocycles in medicinal chemistry.
2-Bromo-N-methylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to access biologically relevant pyridine derivatives. Its bromo group facilitates efficient Suzuki, Stille, and Negishi couplings, while the N-methylpyridin-4-amine moiety provides a basic nitrogen for further functionalization or metal coordination. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis workflows in drug discovery.
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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: