Cu-catalyzed decarboxylative iodination of aryl carboxylic acids with NaI: A practical entry to aryl iodides under aerobic conditions was written by Fu, Zhengjiang;Jiang, Yongqing;Jiang, Ligao;Li, Zhaojie;Guo, Shengmei;Cai, Hu. And the article was included in Tetrahedron Letters in 2018.Recommanded Product: 4-Chloro-2-iodo-1-nitrobenzene This article mentions the following:
A simple and practical Cu-catalyzed decarboxylative iodination has been well established under aerobic condition, which provides a useful method to synthesize aryl iodides in moderate to good yields with the use of (hetero)aryl carboxylic acids and NaI as starting materials [e.g., 4-chloro-2-nitrobenzoic acid â?4-chloro-1-iodo-2-nitrobenzene (80%) using NaI in presence of Cu(OAc)2, 1,10-Phen and O2 in DMSO]. Thiabendazole has been prepared via a three-step procedure to show synthetic practicability of the protocol. In the experiment, the researchers used many compounds, for example, 4-Chloro-2-iodo-1-nitrobenzene (cas: 160938-18-1Recommanded Product: 4-Chloro-2-iodo-1-nitrobenzene).
4-Chloro-2-iodo-1-nitrobenzene (cas: 160938-18-1) belongs to iodide derivatives. Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics. Polyiodoorganic compounds are sometimes employed as X-ray contrast agents, in fluoroscopy, a type of medical imaging. This application exploits the X-ray absorbing ability of the heavy iodine nucleus.Recommanded Product: 4-Chloro-2-iodo-1-nitrobenzene
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com