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Structure of 1246184-55-3
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7-Bromo-3-iodoimidazo[1,2-a]pyridine features a dual halogenated imidazopyridine core, enabling efficient cross-coupling reactions in medicinal chemistry. The electron-deficient aromatic system pairs well with palladium catalysts, while the bromo and iodo substituents offer orthogonal reactivity for sequential functionalization. This scaffold supports rapid diversification in target-oriented synthesis.
7-Bromo-3-iodoimidazo[1,2-a]pyridine serves as a versatile bifunctional building block for the construction of imidazo[1,2-a]pyridine scaffolds in medicinal chemistry and catalytic synthesis. The bromo and iodo substituents enable sequential cross-coupling reactions with high chemoselectivity, facilitating access to complex heterocyclic architectures. Its bench-stable nature and compatibility with palladium-catalyzed coupling protocols make it well-suited for iterative functionalization in API development workflows.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: