《Pd-Catalyzed protecting-group-free cross-couplings of iodophenols with atom-economic triarylbismuth reagents》 was written by Rao, Maddali L. N.; Meka, Suresh. Product Details of 626-02-8This research focused onunsym hydroxybiaryl preparation; iodophenol triarylbismuth reagent cross coupling palladium catalyst. The article conveys some information:
An efficient protocol for the protecting-group-free synthesis of unsym. hydroxybiaryls ArAr1 [Ar = Ph, 4-MeC6H4, 4-FC6H4, etc.; Ar1 = 2-HOC6H4, 4-HOC6H4, 2-HO-5-BrC6H3, etc.] via the Pd-catalyzed cross-couplings of unprotected iodophenols with triarylbismuth reagents was described. The presented protocols exhibited good to high yields of hydroxybiaryls. In addition to this study using 3-Iodophenol, there are many other studies that have used 3-Iodophenol(cas: 626-02-8Product Details of 626-02-8) was used in this study.
3-Iodophenol(cas: 626-02-8) belongs to organic iodides. Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine.Product Details of 626-02-8 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.
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com