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Structure of 1194374-75-8
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8-Bromo-2-methylimidazo[1,2-a]pyridine features a fused heterocyclic core combining imidazo[1,2-a]pyridine with bromo and methyl substituents at the 8- and 2-positions, respectively. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions and serves as a key building block in medicinal chemistry for kinase inhibitors and bioactive scaffolds.
8-Bromo-2-methylimidazo[1,2-a]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of imidazo[1,2-a]pyridine scaffolds via palladium-catalyzed cross-coupling reactions. Its bromine at the C8 position provides a reliable site for further functionalization, while the methyl group enhances solubility and modulates electronic properties. The compound exhibits excellent bench stability and compatibility with standard synthetic protocols, facilitating scalable synthesis of potential kinase inhibitors and other bioactive molecules.
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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: