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  2. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    Bromoethane, also known as ethyl bromide, is a chemical compound of the haloalkanes group. It is abbreviated by chemists as EtBr (which is also used as an abbreviation for ethidium bromide ). This volatile compound has an ether-like odor.

  3. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.

  4. 2-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopropane

    Download as PDF; Printable version; ... Bromoethane; 1-Bromopropane ... It is used for introducing the isopropyl functional group in organic synthesis. 2-Bromopropane ...

  5. File:Bromoethane SN2 reaction.svg - Wikipedia

    en.wikipedia.org/wiki/File:Bromoethane_SN2...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  6. Bromomethane - Wikipedia

    en.wikipedia.org/wiki/Bromomethane

    Bromomethane, commonly known as methyl bromide, is an organobromine compound with formula C H 3 Br.This colorless, odorless, nonflammable gas is produced both industrially and biologically.

  7. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide used to study the massive deadenylation of adenine based-nucleosides induced by halogenated alkanes (alkyl halides) under physiological conditions. 2-Bromo-2-methylpropane causes the massive deguanylation of guanine based-nucleosides and massive deadenylation of adenine based-nucleosides.

  8. 1-Bromo-4-iodobenzene - Wikipedia

    en.wikipedia.org/wiki/1-bromo-4-iodobenzene

    Since aryl iodides are more reactive than aryl bromides in the Sonogashira coupling, [4] the iodine end of 1-bromo-4-iodobenzene can be selectively coupled to a terminal acetylene while leaving the bromine end unreacted, by running the reaction at room temperature.

  9. Tetraethylammonium bromide - Wikipedia

    en.wikipedia.org/wiki/Tetraethylammonium_bromide

    Download as PDF; Printable version; ... Interactive image; ChEMBL: ChEMBL324254 ... but is also used in organic chemical synthesis. Chemistry