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Structure of 89581-84-0
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2-Chloro-3-(chloromethyl)pyridine features a chloromethyl group flanked by an electron-deficient pyridine ring and a pendant chlorine, enabling selective functionalization in heterocyclic synthesis. This bifunctional scaffold facilitates efficient coupling reactions under mild conditions, offering enhanced reactivity for constructing complex nitrogen-containing architectures in medicinal chemistry and materials science applications.
2-Chloro-3-(chloromethyl)pyridine serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient construction of nitrogen-containing heterocycles and functionalized pharmaceutical scaffolds. The chloromethyl group exhibits high reactivity in nucleophilic substitution reactions, while the 2-chloropyridine moiety provides a handle for palladium-catalyzed cross-coupling processes. Its bench-stable nature and compatibility with diverse reaction conditions make 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 : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: