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Structure of 884660-47-3
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6-Fluoro-5-iodopyridin-2-amine features a strategically positioned fluorine and iodine substituent on the pyridine core, enabling selective cross-coupling reactions. The electron-deficient ring facilitates palladium-catalyzed transformations, while the primary amine group offers direct functionalization potential. This compound serves as a key building block in the synthesis of bioactive heterocycles and pharmaceutical intermediates.
6-Fluoro-5-iodopyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal reactivity profile. The fluorine and iodine substituents allow sequential functionalization, while the pyridin-2-amine moiety provides a handle for further derivatization. Its bench-stable nature and compatibility with standard coupling conditions make it ideal for constructing complex heterocyclic scaffolds in API development.
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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: