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Structure of 79055-64-4
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2-Chloro-3-methylpyridin-4-amine features a pyridine core functionalized with chlorine, methyl, and primary amine groups at strategic positions. This arrangement enables selective coupling reactions in medicinal chemistry and materials synthesis. The electron-deficient ring facilitates nucleophilic substitution, while the amine group offers a handle for derivatization under mild conditions.
2-Chloro-3-methylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds through palladium-catalyzed cross-coupling reactions. Its chlorine atom facilitates reliable functionalization under standard Suzuki, Stille, or Buchwald–Hartwig conditions, while the amino and methyl groups offer orthogonal reactivity for further derivatization. The compound exhibits good bench stability and is readily purified by recrystallization or chromatography, making it well-suited for scalable synthesis and process development.
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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: