Greener, Andrew J.; Ubysz, Patrycja; Owens-Ward, Will; Smith, George; Ocana, Ivan; Whitwood, Adrian C.; Chechik, Victor; James, Michael J. published an article in 2021. The article was titled 《Radical-anion coupling through reagent design: hydroxylation of aryl halides》, and you may find the article in Chemical Science.Application In Synthesis of 3-Iodophenol The information in the text is summarized as follows:
The design and development of an oxime-based hydroxylation reagent, which can chemoselectively convert aryl halides (X = F, Cl, Br, I) into phenols under operationally simple, transition-metal-free conditions was described. Key to the success of this approach was the identification of a reducing oxime anion which can interact and couple with open-shell aryl radicals. Exptl. and computational studies support the proposed radical-nucleophilic substitution chain mechanism. The experimental process involved the reaction of 3-Iodophenol(cas: 626-02-8Application In Synthesis of 3-Iodophenol)
3-Iodophenol(cas: 626-02-8) belongs to organic iodides. Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine.Application In Synthesis of 3-Iodophenol In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs.
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com