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Structure of 401892-47-5
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5-Bromo-2-chloro-4-iodopyridine features a trihalogenated pyridine core with distinct halogen positions enabling selective cross-coupling reactions. The strategic placement of bromo, chloro, and iodo substituents supports sequential functionalization in transition-metal-catalyzed processes. This molecule delivers high reactivity and orthogonal handle compatibility for complex heterocyclic synthesis under standard conditions.
5-Bromo-2-chloro-4-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, making it ideal for iterative synthesis in medicinal chemistry and agrochemical research.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: