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Structure of 439146-20-0
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6-Chloro-4-methoxypyridin-2-amine features a pyridine core functionalized with chlorine and methoxy groups, enabling selective coupling in medicinal chemistry. The electron-deficient ring facilitates nucleophilic substitution, while the amine handle supports efficient derivatization under standard conditions. This scaffold offers enhanced metabolic stability and solubility for drug discovery applications.
6-Chloro-4-methoxypyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through palladium-catalyzed cross-coupling reactions. Its chlorine and amine functionalities offer orthogonal reactivity for late-stage diversification, while the methoxy group enhances solubility and modulates electronic properties. Bench-stable and readily purified by column chromatography, it facilitates robust synthesis of kinase inhibitors and other bioactive heterocycles.
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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: