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Structure of 885950-21-0
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3-Bromoimidazo[1,2-a]pyridine-6-carbonitrile features a rigid fused heterocyclic core with complementary electrophilic (bromine) and nucleophilic (cyano) sites. This arrangement enables seamless integration into cross-coupling reactions and modular synthesis of bioactive imidazopyridine scaffolds under standard conditions.
3-Bromoimidazo[1,2-a]pyridine-6-carbonitrile serves as a versatile heterocyclic building block for medicinal chemistry and catalytic cross-coupling. The bromine and nitrile groups enable sequential functionalization via palladium-catalyzed reactions, while the imidazopyridine core provides structural rigidity and favorable pharmacophore properties. Bench-stable and compatible with standard purification methods, it facilitates efficient synthesis of complex nitrogen-containing scaffolds relevant to drug discovery programs.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: