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Structure of 18368-63-3
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2-Chloro-6-methylpyridine is a bench-stable, electron-deficient heterocycle featuring a chlorine atom at the 2-position and a methyl group at the 6-position. This regioselective substitution pattern enables direct functionalization in cross-coupling reactions, facilitating efficient access to complex pyridyl architectures in medicinal chemistry and agrochemical synthesis.
2-Chloro-6-methylpyridine serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-established reactivity at the chlorine site. The methyl group provides a handle for further functionalization, while the pyridine core offers favorable electronic properties for heterocyclic scaffold construction. Its bench stability and compatibility with standard reaction conditions make it a reliable choice for medicinal chemistry and process development workflows.
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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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: