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Structure of 51564-92-2
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6-Chloro-4-methylpyridin-2-amine features a pyridine core functionalized with chlorine at C6 and a methyl group at C4, enabling precise tuning of electronic properties. The ortho-chloro and para-methyl substitutions create a sterically constrained, electron-deficient platform ideal for coupling reactions. This scaffold integrates readily into pharmaceutical intermediates and agrochemicals, offering enhanced metabolic stability and targeted reactivity in synthetic pathways.
6-Chloro-4-methylpyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through palladium-catalyzed cross-coupling reactions. The chlorine atom facilitates reliable Suzuki, Stille, or Negishi coupling, while the pyridine nitrogen and methyl group offer orthogonal reactivity for further functionalization. Bench-stable and readily purified by standard techniques, it supports scalable synthesis of kinase inhibitors and other bioactive compounds.
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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: