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Structure of 319474-34-5
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4-Iodo-1H-pyrrolo[2,3-b]pyridine features a fused heterocyclic core with a strategically positioned iodine atom enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into complex molecular architectures, offering enhanced stability under standard conditions for synthetic applications in medicinal chemistry and materials science.
4-Iodo-1H-pyrrolo[2,3-b]pyridine serves as a versatile building block for constructing biologically relevant heterocycles via palladium-catalyzed cross-coupling reactions. The iodide group enables reliable Suzuki, Stille, and Negishi couplings, while the pyrrolopyridine core provides a rigid, electron-deficient scaffold suitable for medicinal chemistry applications. Bench-stable and readily purified by flash chromatography, it functions effectively in multi-step synthesis workflows requiring functional group tolerance and predictable reactivity.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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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-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P362-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: