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Structure of 159783-22-9
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3,5-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 amine group provides a versatile handle for derivatization, while the difluoro substitution imparts metabolic stability and improved membrane permeability. This compound serves as a key building block in medicinal chemistry and agrochemical synthesis.
3,5-Difluoropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 4-position via palladium-catalyzed cross-coupling reactions. Its difluoro substitution enhances metabolic stability and modulates electronic properties, while the primary amine facilitates derivatization through acylation, sulfonation, or reductive amination. Bench-stable and compatible with standard purification methods, it functions reliably in the construction of bioactive heterocycles and kinase inhibitor scaffolds.
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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: