Martins, Nayara Silva published the artcileDibromination of alkenes with LiBr and H2O2 under mild conditions, Formula: C6H12Br2, the publication is New Journal of Chemistry (2018), 42(1), 161-167, database is CAplus.
Electron-rich and electron-poor alkenes, and alkenes bearing protecting groups can be efficiently and stereoselectively converted to trans-dibromides using LiBr/H2O2 and AcOH as a proton source in 1,4-dioxane. For most substrates addition of 0.1 mol% of PhTeTePh enhances the reaction rate and the yield of the products. Exptl. data suggest that the brominating agent prepared in situ is mol. bromine and that LiBr assists the activation of H2O2 allowing bromination to occur using AcOH as a mild proton source in uncatalyzed experiments Scale-up is feasible: 10.0 mmol of 1-octene was quant. converted to 1,2-dibromooctene in one hour of reaction at room temperature
New Journal of Chemistry published new progress about 594-81-0. 594-81-0 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 2,3-Dibromo-2,3-dimethylbutane, and the molecular formula is C6H12Br2, Formula: C6H12Br2.
Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary