Functionalization of Quinolines through Copper-Catalyzed Regioselective Halogenation Reaction was written by Sahoo, Harekrishna;Ramakrishna, Isai;Baidya, Mahiuddin. And the article was included in ChemistrySelect in 2016.Safety of 3-(Trifluoromethyl)benzene-1-sulfonyl chloride This article mentions the following:
A copper-catalyzed chelation-controlled remote C-H halogenation of quinolines is developed. The reaction is scalable and proceeded with excellent C5-regioselectivity offering halogen-substituted 8-aminoquinolines such as I (R = 2-naphthyl, 4-MeOC6H4, PhCH2, t-Bu, etc.; R1 = Br, I) in very high yields (up to 97%). The products were further utilized for various cross-coupling reactions en route to highly C5-functionalized quinolines. As an application, synthesis of a bioactive compound having tumor-suppressor activity was accomplished. In the experiment, the researchers used many compounds, for example, 3-(Trifluoromethyl)benzene-1-sulfonyl chloride (cas: 777-44-6Safety of 3-(Trifluoromethyl)benzene-1-sulfonyl chloride).
3-(Trifluoromethyl)benzene-1-sulfonyl chloride (cas: 777-44-6) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Safety of 3-(Trifluoromethyl)benzene-1-sulfonyl chloride
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics