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Structure of 890092-47-4
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5-Chloro-4-methylpyridin-3-amine features a pyridine core functionalized with a chlorine atom at the 5-position and a methyl group at the 4-position, creating a sterically accessible site for nucleophilic substitution. The electron-deficient heterocycle pairs effectively with amine functionality to enable direct coupling in cross-coupling reactions. This bench-stable compound integrates readily into synthetic pathways requiring halogenated nitrogen heterocycles.
5-Chloro-4-methylpyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds through palladium-catalyzed cross-coupling reactions. The chloro group provides reliable electrophilic reactivity for Suzuki, Stille, and Buchwald–Hartwig transformations, while the pyridin-3-amine functionality offers a handle for further derivatization. Bench-stable and readily purified, it functions effectively in multi-step syntheses requiring functional group tolerance and predictable regiochemistry.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: