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Structure of 1350738-82-7
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5-Bromoimidazo[1,2-a]pyridin-2-amine features a fused heterocyclic core with a bromine atom at the 5-position and an amine group at the 2-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into bioactive molecules, offering high reactivity and stability under standard conditions.
5-Bromoimidazo[1,2-a]pyridin-2-amine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to imidazo[1,2-a]pyridine-based scaffolds prevalent in medicinal chemistry. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the amine functionality supports derivatization via acylation, alkylation, or coupling protocols. The compound exhibits good bench stability and is readily purified by chromatography, making it well-suited for iterative synthesis campaigns in API development.
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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: