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Structure of 79055-62-2
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2-Chloro-5-methylpyridin-4-amine features a pyridine core bearing a chloro group at C2 and a methylamino substituent at C4, delivering a potent electrophilic handle. This electron-deficient heterocycle integrates readily into cross-coupling reactions, enabling efficient access to advanced pharmaceutical intermediates and functionalized materials under standard conditions.
2-Chloro-5-methylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. The chloro group facilitates palladium-catalyzed cross-coupling reactions, while the pyridin-4-amine functionality supports further derivatization via nucleophilic substitution or metal-mediated transformations. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for synthesizing targeted heterocyclic compounds 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: