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Structure of 56051-32-2
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3-Bromo-7-methylimidazo[1,2-a]pyridine is a heteroaromatic building block featuring a bromine substituent at the 3-position and a methyl group at the 7-position. This configuration enables selective functionalization in transition-metal-catalyzed coupling reactions. The compound exhibits enhanced solubility in organic solvents and stability under standard bench conditions, facilitating its integration into complex synthetic sequences for pharmaceutical and agrochemical discovery.
3-Bromo-7-methylimidazo[1,2-a]pyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biologically relevant heterocyclic scaffolds. The bromo group facilitates efficient C–C and C–N bond formation under standard conditions, while the imidazopyridine core provides structural rigidity and favorable pharmacophoric properties. Bench-stable and compatible with diverse functional groups, it functions effectively in modular synthesis workflows for kinase inhibitors and other targeted therapeutics.
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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-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: