Markgraf, J. Hodge et al. published their research in Chemistry & Industry (London, United Kingdom) in 1987 | CAS: 615-55-4

3,4-Dibromoaniline (cas: 615-55-4) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Name: 3,4-Dibromoaniline

Bromination of 3-haloanilines with 2,4,4,6-tetrabromo-2,5-cyclohexadien-1-one was written by Markgraf, J. Hodge;Marshall, G. Thomas;Greeley, Michael A.. And the article was included in Chemistry & Industry (London, United Kingdom) in 1987.Name: 3,4-Dibromoaniline This article mentions the following:

Mixtures of dihaloanilines I, II, and III (R1 = F, Cl, Br, iodo) were obtained from the resp. 3-R1C6H4NH2. In the experiment, the researchers used many compounds, for example, 3,4-Dibromoaniline (cas: 615-55-4Name: 3,4-Dibromoaniline).

3,4-Dibromoaniline (cas: 615-55-4) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Name: 3,4-Dibromoaniline

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary