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Structure of 1303890-45-0
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6-Bromo-7-chloroimidazo[1,2-a]pyridine features a fused heterocyclic core with complementary halogen substituents at the 6- and 7-positions, enabling selective cross-coupling reactions. The electron-deficient pyridine ring enhances reactivity in palladium-catalyzed transformations, while the sterically accessible framework supports efficient functionalization. This scaffold serves as a key building block for bioactive imidazopyridine derivatives in medicinal chemistry.
6-Bromo-7-chloroimidazo[1,2-a]pyridine serves as a versatile building block in medicinal chemistry, enabling the construction of imidazo[1,2-a]pyridine scaffolds via palladium-catalyzed cross-coupling reactions. Its dual halogenation pattern supports sequential functionalization, offering orthogonal reactivity for C–C and C–heteroatom bond formation. The compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for scalable synthesis of bioactive heterocycles.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: