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Structure of 5857-47-6
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3-Bromo-5-methylimidazo[1,2-a]pyridine features a fused heterocyclic core with regioselective bromination at the 3-position and a methyl group at the 5-position. This electron-deficient scaffold enables direct coupling in cross-coupling reactions, serving as a key building block for pharmaceutical intermediates and functional materials under standard conditions.
3-Bromo-5-methylimidazo[1,2-a]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic coupling reactions. The bromine substituent enables palladium-catalyzed cross-coupling transformations, while the methyl group enhances solubility and modulates electronic properties. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical scaffold for constructing complex nitrogen-containing frameworks 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-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: