Unexpected C=N bond formation via NaI-catalyzed oxidative de-tetra-hydrogenative cross-couplings between N,N-dimethyl aniline and sulfamides was written by Zheng, Yang;Mao, Jincheng;Chen, Jie;Rong, Guangwei;Liu, Defu;Yan, Hong;Chi, Yongjian;Xu, Xinfang. And the article was included in RSC Advances in 2015.Related Products of 698-01-1 This article mentions the following:
A direct and convenient C=N bond formation reaction was reported, which was a de-tetra-hydrogenative cross-coupling (DTCC) reaction between N,N-di-Me aniline and sulfamide under transition-metal-free conditions to give sulfonyl amidine derivatives in moderate to high yields. In the experiment, the researchers used many compounds, for example, 2-Chloro-N,N-dimethylaniline (cas: 698-01-1Related Products of 698-01-1).
2-Chloro-N,N-dimethylaniline (cas: 698-01-1) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Related Products of 698-01-1
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics