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  2. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.

  3. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    In the European Union, 1-bromopropane has been classified as reproductive toxicant per Registration, Evaluation, Authorisation and Restriction of Chemicals, which makes it a "substance of very high concern". [12] As of January 5, 2022, 1-bromopropane has been added to the United States Clean Air Act list of Hazardous Air Pollutants (HAP). [13]

  4. Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Butyl_bromide

    2-Bromo-2-methylpropane (tert-butyl bromide) This page was last edited on 5 February 2022, at 12:14 (UTC). Text is available under the Creative Commons Attribution ...

  5. C4H9Br - Wikipedia

    en.wikipedia.org/wiki/C4H9Br

    1-bromo-2-methylpropane This page was last edited on 16 August 2021, at 07:47 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...

  6. 2-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopropane

    2-Bromopropane, also known as isopropyl bromide and 2-propyl bromide, is the halogenated hydrocarbon with the formula CH 3 CHBrCH 3. It is a colorless liquid. It is a colorless liquid. It is used for introducing the isopropyl functional group in organic synthesis . 2-Bromopropane is prepared by heating isopropanol with hydrobromic acid .

  7. 1-Bromo-2,2-dimethylpropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromo-2,2-dimethylpropane

    Hazards GHS labelling: Pictograms. ... 1-Bromo-2,2-dimethylpropane, also known as neopentyl bromide, is an isomer of bromopentane. It is a colorless liquid. [2]

  8. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    2 Li + C 4 H 9 X → C 4 H 9 Li + LiX where X = Cl, Br. The lithium for this reaction contains 1-3% sodium. When bromobutane is the precursor, the product is a homogeneous solution, consisting of a mixed cluster containing both LiBr and LiBu. 1-Fluorobutane can be obtained by reacting 1-bromobutane with potassium fluoride in ethylene glycol. [5]

  9. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    H 2 C=CH 2 + HBr → H 3 C-CH 2 Br. Bromoethane is inexpensive and would rarely be prepared in the laboratory. A laboratory synthesis includes reacting ethanol with a mixture of hydrobromic and sulfuric acids. An alternate route involves refluxing ethanol with phosphorus and bromine; phosphorus tribromide is generated in situ. [4]