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Structure of 63489-58-7
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2,6-Difluoropyridin-4-amine features a fluorinated pyridine core with strategically positioned electron-withdrawing substituents, enhancing its reactivity in cross-coupling and nucleophilic substitution processes. The para-amino group enables direct incorporation into pharmaceutical scaffolds, while the difluoro substitution imparts metabolic stability and improved membrane permeability. This bench-stable compound serves as a key building block for bioactive heterocycles.
2,6-Difluoropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 4-position via nucleophilic substitution due to the activating effect of the fl uorine atoms. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling reactions facilitate efficient access to substituted pyridine scaffolds common in pharmaceutical development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H315-H319-H332-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: