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Structure of 1427439-69-7
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7-Bromoimidazo[1,2-a]pyridin-3-amine serves as a versatile heterocyclic scaffold for medicinal chemistry and catalysis. The bromo substituent enables palladium-catalyzed cross-coupling reactions, while the imidazopyridine core offers enhanced metabolic stability and favorable binding interactions in kinase-targeted drug discovery.
7-Bromoimidazo[1,2-a]pyridin-3-amine serves as a versatile building block for medicinal chemistry and catalytic cross-coupling applications. The bromo group enables palladium-catalyzed transformations such as Suzuki-Miyaura and Buchwald-Hartwig couplings, while the imidazo[1,2-a]pyridine core provides a rigid, electron-deficient heterocyclic scaffold with favorable pharmacokinetic properties. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to complex nitrogen-containing architectures in drug discovery campaigns.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: