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  2. 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 .

  3. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    1-Bromopropane (n-propylbromide or nPB) is a bromoalkane with the chemical formula CH 3 CH 2 CH 2 Br. It is a colorless liquid that is used as a solvent. It has a characteristic hydrocarbon odor.

  4. Propyl group - Wikipedia

    en.wikipedia.org/wiki/Propyl_group

    An isomeric form of propyl is obtained by moving the point of attachment from a terminal carbon atom to the central carbon atom, named isopropyl or 1-methylethyl. To maintain four substituents on each carbon atom, one hydrogen atom has to be moved from the middle carbon atom to the carbon atom which served as attachment point in the n -propyl ...

  5. Isopropyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_alcohol

    Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol) is a colorless, flammable, organic compound with a pungent alcoholic odor. [9]Isopropyl alcohol, an organic polar molecule, is miscible in water, ethanol, and chloroform, demonstrating its ability to dissolve a wide range of substances including ethyl cellulose, polyvinyl butyral, oils, alkaloids, and natural ...

  6. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    Monobromotoluene isomers [1] [2] [3]; Common name Structure Systematic name: 1-bromo-2-methylbenzene 1-bromo-3-methylbenzene 1-bromo-4-methylbenzene Molecular formula

  7. Bromine number - Wikipedia

    en.wikipedia.org/wiki/Bromine_number

    The bromine number is similar to the iodine number, which is a similar technique used in evaluating the unsaturation of fats and fatty acids. Iodine is less reactive toward the tri- and tetra-substituted double bonds, [2] found in petroleum-derived samples. The C=C double bonds in fats and fatty acids are exclusively disubstituted.

  8. 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.

  9. 1-Bromo-2,2-dimethylpropane - Wikipedia

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

    CAS Number. 630-17-1; 3D model . Interactive image; Beilstein Reference. ... also known as neopentyl bromide, is an isomer of bromopentane. It is a colorless liquid. [2]