Chaikovskii, V. K. published the artcileIodination of aromatic compounds with iodine monochloride in aqueous sulfuric acid, Application In Synthesis of 2100-25-6, the main research area is iodination aromatic compound iodine chloride; toluene iodination iodine chloride; chemoselectivity iodination aromatic compound iodine chloride; regioselectivity iodination aromatic compound iodine chloride; alkylbenzene iodination iodine chloride; durene iodination iodine chloride; anisole iodination iodine chloride; aniline iodination iodine chloride.
Iodine monochloride in aqueous sulfuric acid turned out to be a convenient and general reagent for preparative iodination of alkylbenzenes, phenol ethers, and aromatic amines. The relative selectivity and activity of iodine monochloride in aqueous solutions of sulfuric acid with various concentrations were determined using toluene as model substrate. Raising the sulfuric acid concentration results in considerable increase of the electrophilicity of ICI. Effective sulfuric acid concentrations were determined for specific substrate series. Iodine monochloride in aqueous sulfuric acid shows enhanced selectivity in the synthesis of monoiodo derivatives
Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii) published new progress about Aromatic compounds Role: RCT (Reactant), RACT (Reactant or Reagent). 2100-25-6 belongs to class iodides-buliding-blocks, name is 3-Iodo-1,2,4,5-tetramethylbenzene, and the molecular formula is C10H13I, Application In Synthesis of 2100-25-6.
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com