A Practically Unified Electrochemical Strategy for Ni-Catalyzed Decarboxylative Cross-Coupling of Aryl Trimethylammonium Salts was written by Kong, Xianqiang;Chen, Yiyi;Chen, Xiaohui;Lu, Zheng-Xuan;Wang, Wei;Ni, Shao-Fei;Cao, Zhong-Yan. And the article was included in Organic Letters in 2022.SDS of cas: 698-01-1 This article mentions the following:
By merging electrocatalysis and nickel catalysis, a unified strategy was successfully applied for preparing aryl ketones ArC(O)Ph [Ar = Ph, 4-ClC6H4, 4-MeC6H4, etc.], amides ArC(O)NR1R2 [Ar = Ph, 4-ClC6H4, 4-MeC6H4, etc.; R1 = R2 = Me, Et; R1R2 = CH2(CH2)2CH2, CH2CH2OCH2CH2], esters ArC(O)OR [Ar = Ph, 2-MeC6H4, 4-FC6H4, etc.; R = Me, Et] or aldehydes ArCHO [Ar = Ph, 4-MeC6H4, 4-PhC6H4, etc.] via decarboxylative cross-coupling of four types of α-oxocarboxylic acids and their derivatives with aryl trimethylammonium salts under mild conditions. In the experiment, the researchers used many compounds, for example, 2-Chloro-N,N-dimethylaniline (cas: 698-01-1SDS of cas: 698-01-1).
2-Chloro-N,N-dimethylaniline (cas: 698-01-1) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.SDS of cas: 698-01-1
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics