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Structure of 2402-78-0
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2,6-Dichloropyridine features a rigid heteroaromatic core with chlorine substituents at electron-deficient positions, enabling selective electrophilic substitution and serving as a key scaffold in pharmaceutical synthesis. This bench-stable, moisture-tolerant reagent integrates readily into cross-coupling and functionalization workflows.
2,6-Dichloropyridine serves as a versatile building block in synthetic organic chemistry, enabling selective functionalization at the 3- and 4-positions via palladium-catalyzed cross-coupling reactions. Its orthogonal reactivity profile supports efficient construction of substituted heterocycles and pharmaceutical scaffolds. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: