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  2. meso-Stilbene dibromide - Wikipedia

    en.wikipedia.org/wiki/Meso-stilbene_dibromide

    Print/export Download as PDF; Printable version; In other projects ... meso-1,2-dibromo-1,2-diphenyl ethane. Identifiers CAS Number. 13440-24-9; 3D model .

  3. (E)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(E)-Stilbene

    Bromination of trans-stilbene produces predominantly meso-1,2-dibromo-1,2-diphenylethane (sometimes called meso-stilbene dibromide), in line with a mechanism involving a cyclic bromonium ion intermediate of a typical electrophilic bromine addition reaction; [21] cis-stilbene yields a racemic mixture of the two enantiomers of 1,2-dibromo-1,2 ...

  4. 1,2-Dibromoethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Dibromoethane

    1,2-Dibromoethane has wider applications in the preparation of other organic compounds including those carrying modified diazocine rings [9] and vinyl bromide that is a precursor to some fire retardants. [4] In organic synthesis, 1,2-dibromoethane is used to brominate carbanions and to activate magnesium for certain Grignard reagents.

  5. Diphenylacetylene - Wikipedia

    en.wikipedia.org/wiki/Diphenylacetylene

    Reaction of diphenylacetylene with tetraphenylcyclopentadienone results in the formation of hexaphenylbenzene in a Diels–Alder reaction. [4]Dicobalt octacarbonyl catalyzes alkyne trimerisation of diphenylacetylene to form hexaphenylbenzene.

  6. Dibromophenol - Wikipedia

    en.wikipedia.org/wiki/Dibromophenol

    Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; ... 1,2-Dibromo-4-hydroxybenzene 3,5-Dibromophenol, 1,3-Dibromo-

  7. Naled - Wikipedia

    en.wikipedia.org/wiki/Naled

    [3] [4] Its chemical name is dimethyl 1,2-dibromo-2,2-dichloroethylphosphate. Naled is stable in anhydrous condition and must be stored away from light. It must also be stored under normal pressure and temperatures. It degrades in the presence of water and alkali, and produces toxic chloride fumes if exposed to acids or acidic fumes.

  8. Benzil - Wikipedia

    en.wikipedia.org/wiki/Benzil

    Benzil (i.e. Bz 2, systematically known as 1,2-diphenylethane-1,2-dione) is the organic compound with the formula (C 6 H 5 CO) 2, generally abbreviated (PhCO) 2. This yellow solid is one of the most common diketones. Its main use is as a photoinitiator in polymer chemistry. [4]

  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.