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Structure of 1260825-69-1
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2-Bromo-7-chloroimidazo[1,2-a]pyridine features a fused heterocyclic core with complementary halogen substituents enabling selective cross-coupling reactions. The bromine at the 2-position and chlorine at the 7-position provide orthogonal reactivity for sequential functionalization. This scaffold delivers high stability under standard conditions and integrates readily into advanced pharmaceutical intermediates.
2-Bromo-7-chloroimidazo[1,2-a]pyridine serves as a versatile building block in medicinal chemistry, enabling efficient construction of imidazo[1,2-a]pyridine-based scaffolds. Its complementary halogenation pattern facilitates palladium-catalyzed cross-coupling reactions, including Suzuki and Buchwald–Hartwig aminations, with excellent functional group tolerance and bench stability. The compound is particularly useful for late-stage diversification in the synthesis of kinase inhibitors and other 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: