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  2. Dimethylbutadiene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutadiene

    Dimethylbutadiene, formally referred to as 2,3-dimethyl-1,3-butadiene, is an organic compound with the formula (CH 3) 2 C 4 H 4. It is colorless liquid which served an important role in the early history of synthetic rubber .

  3. Dimethylbutene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutene

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... 2,3-Dimethyl-1-butene; 3,3-Dimethyl-1-butene;

  4. 2,3-Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylbutane

    Download as PDF; Printable version; ... 2,3-Dimethylbutane Skeletal formula of 2,3-dimethylbutane with some implicit hydrogens shown ... data are given for materials ...

  5. 2,3-Dimethyl-1-butene - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethyl-1-butene

    2,3-Dimethyl-1-butene is an organic compound with the formula CH 2 =C(CH 3)CH(CH 3) 2. Like the other isomers of dimethylbutene, it is a colorless liquid. Together with 2,3-dimethyl-2-butene it can be produced by dimerization of propylene. It is a precursor to the commercial fragrance tonalide. [1]

  6. Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutane

    Download as PDF; Printable version; In other projects Wikidata item; ... Dimethylbutane (DMB) may refer to: 2,2-Dimethylbutane; 2,3-Dimethylbutane; See also

  7. 3,3-Dimethyl-1-butanol - Wikipedia

    en.wikipedia.org/wiki/3,3-Dimethyl-1-butanol

    Download as PDF; Printable version; In other projects Wikimedia Commons; ... data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

  8. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  9. DMDNB - Wikipedia

    en.wikipedia.org/wiki/DMDNB

    DMDNB, or also DMNB, chemically 2,3-dimethyl-2,3-dinitrobutane, is a volatile organic compound used as a detection taggant for explosives, mostly in the United States where it is virtually the only such taggant in use.