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Structure of 2051921-49-2
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2,6-Dichloro-3-fluoropyridin-4-amine features a pyridine core functionalized with chlorine and fluorine substituents at electron-deficient positions, enabling high reactivity in cross-coupling and nucleophilic substitution reactions. The para-chloro groups facilitate palladium-catalyzed coupling, while the fluorine enhances electrophilicity. This compound serves as a key building block in pharmaceutical synthesis due to its stability and compatibility with diverse reaction conditions.
2,6-Dichloro-3-fluoropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. Its orthogonal reactivity profile—driven by the electron-deficient pyridine core and strategically positioned halogen atoms—facilitates sequential functionalization. The compound exhibits excellent bench stability and compatibility with common protecting groups, making it well-suited for multi-step synthesis and API development 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: