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Structure of 42779-56-6
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2,4-Dichloro-6-methylpyridine serves as a key heterocyclic scaffold in medicinal chemistry and agrochemical synthesis. The electron-deficient pyridine ring, flanked by two chlorine substituents and a methyl group at the 6-position, enables selective coupling reactions. This configuration enhances reactivity in cross-coupling processes while maintaining stability under standard reaction conditions.
2,4-Dichloro-6-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling selective functionalization at the 3- and 5-positions via palladium-catalyzed cross-coupling. Its ortho-chlorine atoms exhibit high reactivity in nucleophilic substitution reactions, while the methyl group provides a stable handle for further derivatization. The compound demonstrates excellent bench stability and compatibility with standard purification methods, facilitating efficient incorporation into complex heterocyclic scaffolds 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: