An article Trifluoromethyl Sulfoxides: Reagents for Metal-Free C-H Trifluoromethylthiolation WOS:000548332600001 published article about NUCLEOPHILIC ORTHO-ALLYLATION; ELECTROPHILIC TRIFLUOROMETHYLTHIOLATION; SODIUM TRIFLUOROMETHANESULFINATE; SELECTIVE TRIFLUOROMETHYLTHIOLATION; INTERRUPTED PUMMERER; ARYL SULFOXIDES; ACID; FUNCTIONALIZATION; DERIVATIVES; 2ND-GENERATION in [Wang, Dong; Carlton, C. Grace; Tayu, Masanori; McDouall, Joseph J. W.; Perry, Gregory J. P.; Procter, David J.] Univ Manchester, Dept Chem, Oxford Rd, Manchester M13 9PL, Lancs, England; [Tayu, Masanori] Meiji Pharmaceut Univ, Dept Chem, 2-522-1 Noshio, Tokyo 2048588, Japan in 2020, Cited 99. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0. HPLC of Formula: C8H10O2
Trifluoromethyl sulfoxides are a new class of trifluoromethylthiolating reagent. The sulfoxides engage in metal-free C-H trifluoromethylthiolation with a range of (hetero)arenes. The method is also applicable to the functionalization of important compound classes, such as ligand derivatives and polyaromatics, and in the late-stage trifluoromethylthiolation of medicines and agrochemicals. The isolation and characterization of a sulfonium salt intermediate supports an interrupted Pummerer reaction mechanism.
HPLC of Formula: C8H10O2. About 1,3-Dimethoxybenzene, If you have any questions, you can contact Wang, D; Carlton, CG; Tayu, M; McDouall, JJW; Perry, GJP; Procter, DJ or concate me.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com