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Structure of 39621-00-6
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2,6-Dichloro-4-methylpyridine is a chlorinated pyridine derivative featuring two chlorine substituents at the 2 and 6 positions and a methyl group at the 4 position. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling direct functionalization at the 3 and 5 ring positions via cross-coupling reactions. Its bench-stable nature and compatibility with palladium-catalyzed transformations streamline synthesis of complex pharmaceutical intermediates.
2,6-Dichloro-4-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of nitrogen-containing heterocycles. Its electrophilic C2 and C6 positions facilitate palladium-catalyzed cross-coupling reactions, while the methyl group provides a site for oxidation or functionalization. The compound exhibits good bench stability and compatibility with common protecting groups, making it suitable for multi-step synthetic sequences.
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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: