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Structure of 1146615-52-2
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3-Bromo-6-iodoimidazo[1,2-a]pyridine features a dual halogenated imidazo[1,2-a]pyridine core, enabling selective cross-coupling reactions. The bromo and iodo substituents offer complementary reactivity in palladium-catalyzed transformations, facilitating efficient construction of complex heterocyclic architectures. This bench-stable compound serves as a pivotal scaffold for medicinal chemistry and materials science applications.
3-Bromo-6-iodoimidazo[1,2-a]pyridine serves as a versatile bifunctional building block for the construction of imidazo[1,2-a]pyridine-based scaffolds in medicinal chemistry and materials science. The orthogonal halogen reactivity enables sequential cross-coupling transformations, facilitating efficient diversification at both C3 and C6 positions. Bench-stable and compatible with standard Pd-catalyzed coupling conditions, it supports reliable synthesis of complex heterocycles with high functional group tolerance.
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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: