Singh, Anoop S.’s team published research in Synthesis in 2019 | CAS: 88-67-5

2-Iodobenzoic acid(cas: 88-67-5) belongs to organic iodides. Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond.Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Safety of 2-Iodobenzoic acid

In 2019,Synthesis included an article by Singh, Anoop S.; Agrahari, Anand K.; Mishra, Nidhi; Singh, Mala; Tiwari, Vinod K.. Safety of 2-Iodobenzoic acid. The article was titled 《An Improved N-Acylation of 1H -Benzotriazole Using 2,2′-Dipyridyldisulfide and Triphenylphosphine》. The information in the text is summarized as follows:

A novel path was developed for the conversion of carboxylic acids into the corresponding N-acylbenzotriazoles by using 2,2′-dipyridyl disulfide/PPh3 in anhydrous dichloromethane in the presence of 1H-benzotriazole. Mild reaction conditions, short reaction time, easy in handling, wide substrate scope, availability of reagents involved and moreover avoiding the use of base made this protocol quite useful for the laboratory practices for N-acylbenzotriazole synthesis. The experimental process involved the reaction of 2-Iodobenzoic acid(cas: 88-67-5Safety of 2-Iodobenzoic acid)

2-Iodobenzoic acid(cas: 88-67-5) belongs to organic iodides. Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond.Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Safety of 2-Iodobenzoic acid

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com