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Structure of 928653-73-0
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5-Bromo-2-chloro-3-iodopyridine features a trihalogenated pyridine core with distinct halogen positions enabling selective cross-coupling reactions. The ortho-chloro and meta-bromo substituents enhance reactivity in palladium-catalyzed transformations, while the iodine moiety serves as a high-efficiency coupling handle. This compound demonstrates robust stability under standard bench conditions and integrates readily into complex molecular architectures.
5-Bromo-2-chloro-3-iodopyridine serves as a versatile trihalogenated pyridine building block for transition-metal-catalyzed cross-coupling reactions. Its orthogonal halogen reactivity enables sequential functionalization at distinct positions, facilitating the construction of complex heterocyclic scaffolds. The molecule exhibits excellent bench stability and compatibility with palladium-catalyzed coupling protocols, supporting efficient access to diversified pyridine-based architectures in medicinal chemistry and materials science applications.
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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-H319
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: