In 2019,Chinese Journal of Chemistry included an article by Hong, Junting; Liu, Qianyi; Li, Feng; Bai, Guangcan; Liu, Guoquan; Li, Man; Nayal, Onkar S.; Fu, Xuefeng; Mo, Fanyang. Recommanded Product: 1-Iodonaphthalene. The article was titled 《Electrochemical Radical Borylation of Aryl Iodides》. The information in the text is summarized as follows:
Summary of main observation and conclusion : Herein, we report the first electrochem. strategy for the borylation of aryl iodides via a radical pathway using current as a driving force. A mild reaction condition allows an assorted range of readily available aryl iodides to be proficiently converted into synthetically valuable arylboronic esters under transition metal catalyst-free conditions. Moreover, this method also shows good functional group tolerance. Initial control mechanistic experiments reveal the formation of aryl radical as a key intermediate and the current plays an important role in the generation of radical intermediate. The results came from multiple reactions, including the reaction of 1-Iodonaphthalene(cas: 90-14-2Recommanded Product: 1-Iodonaphthalene)
1-Iodonaphthalene(cas: 90-14-2) is one of organic iodides. Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine. 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. Oceanic alkyl iodides are believed to be the principal source of atmospheric iodine.Recommanded Product: 1-Iodonaphthalene
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com