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  2. 1,9-Dibromononane - Wikipedia

    en.wikipedia.org/wiki/1,9-Dibromononane

    1,9-Dibromononane is a chemical compound used in the synthesis of the carbamate nerve agent EA-4056. [1] References This page was last edited on 10 October ...

  3. Bromine pentafluoride (data page) - Wikipedia

    en.wikipedia.org/wiki/Bromine_pentafluoride...

    1 Material Safety Data Sheet. 2 Structure and properties. ... This page provides supplementary chemical data on bromine pentafluoride. Material Safety Data Sheet

  4. Bromine trifluoride (data page) - Wikipedia

    en.wikipedia.org/wiki/Bromine_trifluoride_(data...

    1 Material Safety Data Sheet. 2 Structure and properties. ... This page provides supplementary chemical data on bromine trifluoride. Material Safety Data Sheet

  5. Dibromomethane - Wikipedia

    en.wikipedia.org/wiki/Dibromomethane

    6 CH 2 BrCl + 3 Br 2 + 2 Al → 6 CH 2 Br 2 + 2 AlCl 3 CH 2 BrCl + HBr → CH 2 Br 2 + HCl. In the laboratory, it is prepared from bromoform using sodium arsenite and sodium hydroxide: [4] CHBr 3 + Na 3 AsO 3 + NaOH → CH 2 Br 2 + Na 3 AsO 4 + NaBr. Another way is to prepare it from diiodomethane and bromine.

  6. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    EuBr 3 + ⁠ 1 / 2 ⁠ H 2 → EuBr 2 + HBr 2 TaBr 4 TaBr 3 + TaBr 5. Most of the bromides of the pre-transition metals (groups 1, 2, and 3, along with the lanthanides and actinides in the +2 and +3 oxidation states) are mostly ionic, while nonmetals tend to form covalent molecular bromides, as do metals in high oxidation states from +3 and above.

  7. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    This can be seen from the standard electrode potentials of the X 2 /X − couples (F, +2.866 V; Cl, +1.395 V; Br, +1.087 V; I, +0.615 V; At, approximately +0.3 V). Bromination often leads to higher oxidation states than iodination but lower or equal oxidation states to chlorination.

  8. Cyanogen bromide - Wikipedia

    en.wikipedia.org/wiki/Cyanogen_bromide

    2 NaCN + Br 2 → (CN) 2 + 2 NaBr (CN) 2 + Br 22 (CN)Br. When refrigerated the material has an extended shelflife. Like some other cyanogen compounds, cyanogen bromide undergoes an exothermic trimerisation to cyanuric bromide ((BrCN) 3). This reaction is catalyzed by traces of bromine, metal salts, acids and bases.

  9. DBDMH - Wikipedia

    en.wikipedia.org/wiki/DBDMH

    DBDMH (also known as 1,3-Dibromo-5,5-Dimethylhydantoin) is an organic compound derived from the heterocycle called dimethylhydantoin.This white crystalline compound with a slight bromine odor is widely used as a disinfectant used for drinking water purification, recreational water treatment, as a bleaching agent in pulp and paper mills, and for treating industrial/commercial water cooling systems.