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Structure of 1235993-31-3
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6-Fluoroimidazo[1,2-a]pyridin-3-amine features a fluorinated imidazopyridine core with a primary amine at the 3-position, enabling direct conjugation in medicinal chemistry. The electron-deficient heterocycle enhances binding affinity in kinase inhibitors and other target-directed scaffolds. This bench-stable compound integrates readily into diverse synthetic pathways under standard conditions.
6-Fluoroimidazo[1,2-a]pyridin-3-amine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic synthesis. Its fluorinated imidazopyridine core enables robust coupling reactions and functions as a key scaffold in kinase inhibitor development. The molecule exhibits good bench stability, facilitates efficient derivatization via nucleophilic substitution, and demonstrates favorable functional group tolerance in standard 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-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: