Yang, Yu-Ming et al. published their research in Organic Letters in 2019 | CAS: 96558-78-0

3-Bromo-5-chlorophenylamine (cas: 96558-78-0) belongs to organobromine compounds. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Formula: C6H5BrClN

Silver-Mediated Trifluoromethoxylation of (Hetero)aryldiazonium Tetrafluoroborates was written by Yang, Yu-Ming;Yao, Jian-Fei;Yan, Wei;Luo, Zhuangzhu;Tang, Zhen-Yu. And the article was included in Organic Letters in 2019.Formula: C6H5BrClN This article mentions the following:

Here we report a silver-mediated trifluoromethoxylation of (hetero)aryldiazonium tetrafluoroborates by converting an aromatic amino group into an OCF3 group. This method, which can be considered to be a trifluoromethoxylation variation of the classic Sandmeyer-type reaction, uses readily available aryl and heteroaromatic amines as starting materials and AgOCF3 as trifluoromethoxylating reagents. The broad substrate scope and simple, mild reaction condition made this transformation a valuable method in constructing aryl-OCF3 bonds. In the experiment, the researchers used many compounds, for example, 3-Bromo-5-chlorophenylamine (cas: 96558-78-0Formula: C6H5BrClN).

3-Bromo-5-chlorophenylamine (cas: 96558-78-0) belongs to organobromine compounds. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Formula: C6H5BrClN

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary