Electrochemical Sulfoxidation of Thiols and Alkyl Halides was written by Yu, Yi;Wu, Shao-Fen;Zhu, Xiao-Bin;Yuan, Yaofeng;Li, Zhen;Ye, Ke-Yin. And the article was included in Journal of Organic Chemistry in 2022.Synthetic Route of C8H9Cl This article mentions the following:
A green and efficient electrochem. sulfoxidation via the use of readily available materials, i.e., thiols and alkyl halides was reported. The simple operation, mild conditions and broad substrate scope render this protocol potentially applicable for the preparation of diverse synthetically significant sulfoxides RSOCH2R1 [R = i-Pr, 4-FC6H4, 4-ClC6H4, etc.; R1 = (CH2)2CH3, Ph, 3-MeOC6H4, etc.]. In the experiment, the researchers used many compounds, for example, 1-(Chloromethyl)-3-methylbenzene (cas: 620-19-9Synthetic Route of C8H9Cl).
1-(Chloromethyl)-3-methylbenzene (cas: 620-19-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. 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).Synthetic Route of C8H9Cl
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics