enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 1,2-Diaminocyclohexane - Wikipedia

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

    1,2-Diaminocyclohexane (DACH) is an organic compound with the formula (CH 2) 4 (CHNH 2) 2. It is a mixture of three stereoisomers: cis -1,2-diaminocyclohexane and both enantiomers of trans -1,2-diaminocyclohexane. The mixture is a colorless, corrosive liquid, although older samples can appear yellow. It is often called DCH-99 and also DACH.

  3. trans-1,2-Diaminocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Trans-1,2-Diaminocyclohexane

    trans-1,2-Diaminocyclohexane is an organic compound with the formula C 6 H 10 (NH 2) 2. This diamine is a building block for C2 -symmetric ligands that are useful in asymmetric catalysis. [1] A mixture of all three stereoisomers of 1,2-diaminocyclohexane is produced by the hydrogenation of o -phenylenediamine.

  4. Dimedone - Wikipedia

    en.wikipedia.org/wiki/Dimedone

    Dimedone is an organic compound with the formula (CH 3) 2 C(CH 2) 2 (CO) 2 (CH 2). Classified as a cyclic diketone, it is a derivative of 1,3-cyclohexanedione. It is a white solid that is soluble in water, as well as ethanol and methanol. It once was used as a reagent to test for the aldehyde functional group.

  5. Cyclohexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_(data_page)

    Critical point. 554 K (281 °C), 4070 kPa. Std enthalpy change of fusion, Δ fusH o. 2.68 kJ/mol crystal I → liquid. Std entropy change of fusion, Δ fusS o. 9.57 J/ (mol·K) crystal I → liquid. Std enthalpy change of vaporization, Δ vapH o. 32 kJ/mol. Std entropy change of vaporization, Δ vapS o.

  6. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. Methylcyclohexane, as a component of a mixture, is usually dehydrogenated to toluene, which increases the octane rating of gasoline. [4] The conversion of methylcyclohexane to toluene is a classic aromatization reaction. This platinum (Pt)-catalyzed process is practiced on scale in the production of ...

  7. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    2 C 6 H 12 + O 22 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid. The oxidation involves radicals and the intermediacy of the hydroperoxide C 6 H 11 O 2 H. Alternatively, cyclohexanol can be produced by the hydrogenation of phenol ...

  8. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is non-polar. Cyclohexane is a colourless, flammable liquid with a distinctive detergent -like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5]

  9. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    2 H 6 means that there is just one structural isomer of ethanol C 2 H 5 OH, not 6. The eight hydrogens of propane C 3 H 8 are partitioned into two structural equivalence classes (the six on the methyl groups, and the two on the central carbon); therefore there are only two positional isomers of propanol (1-propanol and 2-propanol).