Liu, Yin-Li’s team published research in Tetrahedron in 2018 | CAS: 85366-66-1

3-Bromo-4-(trifluoromethoxy)benzaldehyde(cas: 85366-66-1) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides.Quality Control of 3-Bromo-4-(trifluoromethoxy)benzaldehyde

Quality Control of 3-Bromo-4-(trifluoromethoxy)benzaldehydeOn October 4, 2018 ,《Synthesis of vinyl and electron-deficient aryl trifluoromethyl sulfides via Csp2-OH bond activation with AgSCF3 and n-Bu4NI/KI》 was published in Tetrahedron. The article was written by Liu, Yin-Li; Xu, Xiu-Hua; Qing, Feng-Ling. The article contains the following contents:

Direct dehydroxytrifluoromethylthiolation of enols and electron-deficient phenols with AgSCF3 in the presence of Bu4NI and KI is reported, affording a series of vinyl and aryl trifluoromethyl sulfides in moderate to excellent yields. This work represents a rare example of direct functionalization of Csp2-OH bonds.3-Bromo-4-(trifluoromethoxy)benzaldehyde(cas: 85366-66-1Quality Control of 3-Bromo-4-(trifluoromethoxy)benzaldehyde) was used in this study.

3-Bromo-4-(trifluoromethoxy)benzaldehyde(cas: 85366-66-1) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides.Quality Control of 3-Bromo-4-(trifluoromethoxy)benzaldehyde

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary