Miyake, Junpei’s team published research in Sustainable Energy & Fuels in 2019 | CAS: 625-99-0

1-Chloro-3-iodobenzene(cas: 625-99-0) 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.HPLC of Formula: 625-99-0

The author of 《Quaternized poly(arylene perfluoroalkylene)s (QPAFs) for alkaline fuel cells – a perspective》 were Miyake, Junpei; Miyatake, Kenji. And the article was published in Sustainable Energy & Fuels in 2019. HPLC of Formula: 625-99-0 The author mentioned the following in the article:

The recent progress of our research on quaternized poly(arylene perfluoroalkylene)s (QPAFs) as anion exchange membranes (AEMs) for alk. fuel cell applications is reviewed. First, the effect of the perfluoroalkylene group in the polymer main chains on the AEM properties is discussed. We emphasize that the polymer main chains of QPAFs remain intact in harsh alk. environments, and QPAFs have desirable AEM properties, such as well-developed phase-separated morphol., good anion transport, mech. robustness, and gas barrier properties. We then discuss the effect of the mol. structures of the quaternary ammonium groups on the alk. stability of the QPAF membranes. A number of pendant ammonium head groups are much more alk.-stable than the classical benzyltrimethylammonium groups. A comparison of our QPAFs with other state-of-the-art AEMs implies that well-designed aromatic AEMs are potentially applicable for alk. fuel cells that use hydrogen or hydrazine as a fuel. The experimental part of the paper was very detailed, including the reaction process of 1-Chloro-3-iodobenzene(cas: 625-99-0HPLC of Formula: 625-99-0)

1-Chloro-3-iodobenzene(cas: 625-99-0) 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.HPLC of Formula: 625-99-0

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