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Structure of 1321612-85-4
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3-Fluoro-5-iodopyridin-2-amine features a strategically positioned fluorine and iodine on the pyridine ring, enabling efficient cross-coupling transformations. The electron-deficient heteroaromatic core supports robust reaction compatibility in transition-metal-catalyzed processes. This bench-stable compound serves as a key building block for functionalized pharmaceutical intermediates and advanced materials.
3-Fluoro-5-iodopyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its iodine functionality. The fluorine substituent enhances metabolic stability and modulates electronic properties, while the pyridin-2-amine group provides a handle for further functionalization. Its bench-stable solid form and compatibility with standard coupling protocols facilitate efficient synthesis of complex heterocyclic scaffolds relevant to drug discovery.
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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: