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Structure of 1227602-34-7
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2,3-Difluoropyridin-4-amine delivers a potent electron-deficient pyridine scaffold bearing two strategically positioned fluorine atoms. This configuration enhances metabolic stability and enables direct functionalization at the 4-amino site. The molecule integrates readily into kinase inhibitor scaffolds and other bioactive architectures, offering improved solubility and binding affinity in medicinal chemistry applications.
2,3-Difluoropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 4-position via nucleophilic substitution or Pd-catalyzed coupling. The difluoro substitution pattern enhances metabolic stability and modulates electronic properties, while the primary amine facilitates conjugation with carbonyl electrophiles or incorporation into heterocyclic scaffolds. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step synthesis 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: