Substituted phenylene- and biphenylenemercurials was written by Al-Jabar, N. A. A.;Massey, A. G.. And the article was included in Journal of Organometallic Chemistry in 1984.Safety of 3-Bromo-4-fluorotoluene This article mentions the following:
Treating 1,2-Br2C6H4, its Me derivative, or 1,2-Br2C6H2(OMe)2-4,5 with Na amalgam gave trimeric phenylenemercury derivatives Also, heating 1,2-diiodotetrachlorobenzene with Hg gave trimeric tetrachlorophenylenemercury. Biphenylenemercury (HgC12H8)n, prepared by 2 routes, was also trimeric. In the case of perfluorobiphenylenemercury, trace quantities of the tetramer exist in bulk samples of the trimer. In the experiment, the researchers used many compounds, for example, 3-Bromo-4-fluorotoluene (cas: 452-62-0Safety of 3-Bromo-4-fluorotoluene).
3-Bromo-4-fluorotoluene (cas: 452-62-0) belongs to organobromine compounds. A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. Organobromine compounds have fallen under increased scrutiny for their environmental impact. One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine.Safety of 3-Bromo-4-fluorotoluene
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary