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Structure of 2001563-56-8
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6-Bromo-3-fluoroimidazo[1,2-a]pyridine features a fused heterocyclic core with complementary halogen substituents enabling direct functionalization. The bromine at the 6-position and fluorine at the 3-position offer orthogonal reactivity for palladium-catalyzed cross-coupling and nucleophilic substitution. This electron-deficient scaffold integrates readily into bioactive molecule architectures, particularly in kinase inhibitor development and medicinal chemistry libraries.
6-Bromo-3-fluoroimidazo[1,2-a]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its dual halogenation pattern enables palladium-catalyzed cross-coupling reactions with high regioselectivity, facilitating the construction of complex imidazopyridine scaffolds. The molecule exhibits excellent bench stability, ease of purification, and tolerance to a range of functional groups, making it well-suited for iterative synthesis in API development and small-molecule library generation.
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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: