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Structure of 865604-33-7
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7-Bromoimidazo[1,2-a]pyridin-2-amine features a brominated imidazopyridine core with a pendant amine, enabling direct functionalization in medicinal chemistry. This electron-deficient heterocycle integrates readily into kinase inhibitors and targeted therapeutics, offering high reactivity under standard coupling conditions. The bromo group facilitates Pd-catalyzed cross-coupling, while the amine serves as a handle for conjugation or derivatization.
7-Bromoimidazo[1,2-a]pyridin-2-amine serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient transition-metal-catalyzed couplings and direct functionalization at the C7 position. Its bromine substituent provides high reactivity in Pd-mediated cross-coupling reactions, while the imidazopyridine core offers structural rigidity and favorable pharmacophoric properties. The compound exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for medicinal chemistry campaigns and process development.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: