Mitsudo, Koichi et al. published their research in Organic Letters in 2006 | CAS: 36748-88-6

3-Iodobenzo[b]thiophene (cas: 36748-88-6) belongs to iodide derivatives. Iodide-containing intermediates are common in organic synthesis, because of the easy formation and cleavage of the 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.SDS of cas: 36748-88-6

Selectively Substituted Thiophenes and Indoles by a Tandem Palladium-Catalyzed Multicomponent Reaction was written by Mitsudo, Koichi;Thansandote, Praew;Wilhelm, Thorsten;Mariampillai, Brian;Lautens, Mark. And the article was included in Organic Letters in 2006.SDS of cas: 36748-88-6 This article mentions the following:

A variety of di- and trisubstituted thiophenes were synthesized by a one-pot Pd-catalyzed ortho-alkylation sequence terminated by either Heck or C-H coupling. Thus, reaction of 3-iodothiophene with BuI and H2C:CHCO2CMe3 in acetonitrile containing Pd(OAc)2, tri-2-furylphosphine, norbornene, and Cs2CO3 at 80° for 20 h gave 91% [(butoxycarbonyl)vinyl]thiophene I. Initial results toward the functionalization of indoles were also presented. In the experiment, the researchers used many compounds, for example, 3-Iodobenzo[b]thiophene (cas: 36748-88-6SDS of cas: 36748-88-6).

3-Iodobenzo[b]thiophene (cas: 36748-88-6) belongs to iodide derivatives. Iodide-containing intermediates are common in organic synthesis, because of the easy formation and cleavage of the 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.SDS of cas: 36748-88-6

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