Anodic Oxidation and Organocatalysis: Direct Regio- and Stereoselective Access to meta-Substituted Anilines by α-Arylation of Aldehydes was written by Jensen, Kim L.;Franke, Patrick T.;Nielsen, Lasse T.;Daasbjerg, Kim;Joergensen, Karl Anker. And the article was included in Angewandte Chemie, International Edition in 2010.SDS of cas: 1146-43-6 This article mentions the following:
An anodic oxidation/organocatalytic protocol for α-arylation of aldehydes using substituted electron-rich aromatic compounds provided meta-substituted anilines, e.g. I, in good yields with excellent enantioselectivities. In the experiment, the researchers used many compounds, for example, N-(4-Hydroxyphenyl)-4-methylbenzenesulfonamide (cas: 1146-43-6SDS of cas: 1146-43-6).
N-(4-Hydroxyphenyl)-4-methylbenzenesulfonamide (cas: 1146-43-6) belongs to amides. Amides include many other important biological compounds, as well as many drugs like paracetamol, penicillin and LSD. Low-molecular-weight amides, such as dimethylformamide, are common solvents. Amides are stable compounds. The lower-melting members (such as acetamide) can be readily purified by fractional distillation. Most amides are solids which have low solubilities in water.SDS of cas: 1146-43-6
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics