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Structure of 1509263-23-3
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8-Bromoimidazo[1,2-a]pyridin-2-amine features a fused heterocyclic core with a bromine substituent at the 8-position and a primary amine at the 2-position. This combination enables direct functionalization in cross-coupling reactions and facilitates incorporation into bioactive scaffolds. The molecule exhibits good stability under standard conditions and serves as a key intermediate in medicinal chemistry.
8-Bromoimidazo[1,2-a]pyridin-2-amine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to imidazo[1,2-a]pyridine scaffolds prevalent in kinase inhibitors and CNS-targeted therapeutics. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the amine functionality supports direct derivatization or salt formation, offering excellent bench stability and compatibility with standard purification methods.
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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: