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Structure of 1352898-81-7
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6-Bromo-5-chloroimidazo[1,2-a]pyridine features a fused heterocyclic core with complementary halogenation at the 6-bromo and 5-chloro positions, enabling selective cross-coupling reactions. This electron-deficient imidazopyridine scaffold integrates readily into complex molecular architectures under palladium-catalyzed conditions, offering precise control in medicinal chemistry and materials synthesis.
6-Bromo-5-chloroimidazo[1,2-a]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its dual halogenation pattern enables sequential cross-coupling reactions, facilitating the construction of complex biaryl and triaryl scaffolds. The molecule exhibits excellent bench stability, ease of handling, and compatibility with palladium-catalyzed coupling protocols such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Functional group tolerance supports efficient late-stage derivatization in synthetic workflows.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: