HPLC of Formula: 882-33-7In 2019 ,《Sulfonyl Fluoride Synthesis through Electrochemical Oxidative Coupling of Thiols and Potassium Fluoride》 was published in Journal of the American Chemical Society. The article was written by Laudadio, Gabriele; Bartolomeu, Aloisio de A.; Verwijlen, Lucas M. H. M.; Cao, Yiran; de Oliveira, Kleber T.; Noel, Timothy. The article contains the following contents:
Sulfonyl fluorides are valuable synthetic motifs for a variety of applications, among which sulfur(VI) fluoride exchange-based “”click chem.”” is currently the most prominent. Consequently, the development of novel and efficient synthetic methods to access these functional groups is of great interest. Herein, the authors report a mild and environmentally benign electrochem. approach to prepare sulfonyl fluorides using thiols or disulfides, as widely available starting materials, in combination with KF, as an inexpensive, abundant and safe fluoride source. No addnl. oxidants nor addnl. catalysts are required and, due to mild reaction conditions, the reaction displays a broad substrate scope, including a variety of alkyl, benzyl, aryl and heteroaryl thiols or disulfides. The experimental part of the paper was very detailed, including the reaction process of 1,2-Diphenyldisulfane(cas: 882-33-7HPLC of Formula: 882-33-7)
1,2-Diphenyldisulfane(cas: 882-33-7) belongs to ethers.Although ethers resist hydrolysis, they are cleaved by hydrobromic acid and hydroiodic acid. Hydrogen chloride cleaves ethers only slowly. HPLC of Formula: 882-33-7
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem