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Structure of 381233-75-6
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5-Bromo-3-iodopyridin-2(1H)-one features a dual-halogenated pyridinone core enabling precise cross-coupling transformations. The bromine and iodine substituents offer orthogonal reactivity, facilitating sequential functionalization in complex molecule assembly. This bench-stable scaffold integrates readily into diverse heterocyclic architectures under standard conditions.
5-Bromo-3-iodopyridin-2(1H)-one serves as a versatile dihalogenated pyridinone building block for cross-coupling reactions, enabling efficient access to substituted heterocycles. The bromo and iodo groups exhibit complementary reactivity in palladium-catalyzed coupling protocols, allowing sequential functionalization with high chemoselectivity. Bench-stable and compatible with standard purification methods, it facilitates the synthesis of complex scaffolds in medicinal chemistry and materials science applications.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: