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Structure of 56961-78-5
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2,4-Dichloro-5-methylpyridine serves as a key heterocyclic building block in medicinal chemistry and agrochemical synthesis. The molecule features a pyridine core substituted with chlorine atoms at positions 2 and 4, and a methyl group at position 5, conferring enhanced stability and tailored electronic properties. This combination enables efficient coupling reactions and facilitates the construction of complex functionalized scaffolds under standard conditions.
2,4-Dichloro-5-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The dichloro substitution pattern provides orthogonal reactivity for sequential derivatization, while the methyl group enhances metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with standard reaction conditions facilitate scalable synthesis of complex heterocyclic scaffolds.
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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: