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Structure of 58584-94-4
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2,6-Dichloro-3-methylpyridine offers a sterically accessible pyridine core with dual chlorine substituents at the 2 and 6 positions, enabling selective functionalization. The methyl group at the 3-position enhances electrophilic reactivity while maintaining bench-stable handling characteristics. This configuration facilitates efficient coupling in cross-coupling reactions and serves as a key scaffold for pharmaceutical intermediates requiring halogen-directed substitution patterns.
2,6-Dichloro-3-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling selective functionalization at the pyridine ring due to its electron-deficient nature and regioselective substitution patterns. The methyl group provides a handle for further derivatization, while the dichloro substituents facilitate cross-coupling reactions and nucleophilic aromatic substitution under mild conditions. Its bench-stable, crystalline form simplifies handling and purification in multi-step syntheses.
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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: