In 2019,Organic Letters included an article by Gou, Bo-Bo; Liu, Hang-Fan; Chen, Jie; Zhou, Ling. Recommanded Product: 1-Bromo-3-iodobenzene. The article was titled 《Palladium-Catalyzed Site-Selective C(sp3)-H Arylation of Phenylacetaldehydes》. The information in the text is summarized as follows:
A Pd-catalyzed selective C-H arylation reaction of phenylacetaldehydes using L-valine as the transient directing group, is described.. This process showed a broad substrate scope and excellent selectivity in which a ligand-controlled functionalization of the unactivated β-C(sp3)-H bond. In addition, enantioselective arylation of phenylacetaldehydes was preliminarily explored by utilizing a bulky chiral transient directing group. In the part of experimental materials, we found many familiar compounds, such as 1-Bromo-3-iodobenzene(cas: 591-18-4Recommanded Product: 1-Bromo-3-iodobenzene)
1-Bromo-3-iodobenzene(cas: 591-18-4) has been used in the preparation of 1-(3′-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodec-1-ene and 1-(3′-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene.Recommanded Product: 1-Bromo-3-iodobenzene Further, it is involved in the preparation of oxygen-tethered 1,6-enynes.
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com