Atomfair 6-Fluoro-3-iodo-2-methylpyridine C6H5FIN CAS 884495-23-2

Description

6-Fluoro-3-iodo-2-methylpyridine (CAS No. 884495-23-2) is a high-purity halogenated pyridine derivative with the molecular formula C₆H₅FIN. This compound is a valuable building block in pharmaceutical and agrochemical research, offering a unique combination of fluorine and iodine substituents for selective functionalization. Its IUPAC name is 6-fluoro-3-iodo-2-methylpyridine, and it is also known by synonyms such as 2-fluoro-5-iodo-6-methylpyridine. The presence of both fluorine and iodine atoms makes it an excellent candidate for cross-coupling reactions, nucleophilic substitutions, and other advanced synthetic transformations. This product is rigorously tested for purity and stability, ensuring reliable performance in demanding research applications. Available in various quantities, it is supplied with comprehensive analytical data (including ¹H NMR, ¹³C NMR, and HPLC) to meet the stringent requirements of modern chemical research.

Properties

• CAS Number: 884495-23-2
• Complexity: 99.1
• IUPAC Name: 6-fluoro-3-iodo-2-methyl-pyridine
• InChI: InChI=1S/C6H5FIN/c1-4-5(8)2-3-6(7)9-4/h2-3H,1H3
• InChI Key: VTKNZPBQLMGRJH-UHFFFAOYSA-N
• Exact Mass: 236.94507
• Molecular Formula: C6H5FIN
• Molecular Weight: 237.01
• SMILES: CC1=C(C=CC(=N1)F)I
• Topological: 12.9
• Monoisotopic Mass: 236.94507
• Synonyms: 6-FLUORO-3-IODO-2-METHYLPYRIDINE, 884495-23-2, 2-Fluoro-5-iodo-6-methylpyridine, MFCD08277264, 2-FLUORO-5-IODO-6-METHYL PYRIDINE, SCHEMBL3706044, DTXSID80657718, 6-Fluoro-3-iodo-2-methyl-pyridine, AKOS015891496, AS-30457, SY226256, CS-0152806

Application

6-Fluoro-3-iodo-2-methylpyridine is widely used as a versatile intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates. Its iodine moiety facilitates participation in palladium-catalyzed cross-coupling reactions (e.g., Suzuki, Stille, or Sonogashira couplings) to construct complex heterocyclic systems. The compound’s fluorine atom enhances metabolic stability in bioactive molecules, making it valuable for medicinal chemistry applications. Researchers also employ it in material science for creating specialized ligands and functionalized polymers. Its unique substitution pattern enables precise structural modifications in target molecules.

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