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  2. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a cycloalkane with the molecular formula C 6 H 12. 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).

  3. Cyclohexanehexone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanehexone

    According to X-ray diffraction analysis, the reagent traded under the name "cyclohexanehexone octahydrate" or equivalent names is actually dodecahydroxycyclohexane dihydrate—the geminal diol derivative of the six ketone groups with an additional two molecules of water—a solid that decomposes at 95 °C.

  4. Decalin - Wikipedia

    en.wikipedia.org/wiki/Decalin

    A six-membered ring does not offer sufficient space to start out on an axial position (upwards), and reach the axial position of the neighboring carbon atom, which then will be on the downwards side of the molecule (see the model of cyclohexane in figure 5). The structure is conformationally frozen.

  5. 1,2,4,5-Cyclohexanetetrol - Wikipedia

    en.wikipedia.org/wiki/1,2,4,5-cyclohexanetetrol

    1,2,4,5-Cyclohexanetetrol (also named cyclohexane-1,2,4,5-tetrol, 1,2,4,5-tetrahydroxycyclohexane, or para-cyclohexanetetrol) is an organic compound whose molecule can be described as a cyclohexane with four hydroxyl (OH) groups substituted for hydrogen atoms on two non-adjacent pairs of adjacent carbon atoms. Its formula can be written C 6 H ...

  6. Cyclohexanethiol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanethiol

    It was first prepared by the free-radical reaction of cyclohexane using carbon disulfide as a sulfur source. [1] It is produced industrially by the hydrogenation of cyclohexanone in the presence of hydrogen sulfide over a metal sulfide catalyst: C 6 H 10 O + H 2 S + H 2 → C 6 H 11 SH + H 2 O

  7. Cyclohexyl chloride - Wikipedia

    en.wikipedia.org/wiki/Cyclohexyl_chloride

    Names Preferred IUPAC name ... Cyclohexyl chloride, CyCl. Identifiers CAS Number. 542-18-7 3D model . Interactive image; ... Solubility in water. low Hazards Flash ...

  8. Cyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone

    Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.

  9. 1,2,3,4-Cyclohexanetetrol - Wikipedia

    en.wikipedia.org/wiki/1,2,3,4-Cyclohexanetetrol

    1,2,3,4-Cyclohexanetetrol (also named cyclohexane-1,2,3,4-tetrol, 1,2,3,4-tetrahydroxycyclohexane, or ortho-cyclohexanetetrol) is an organic compound whose molecule can be described as a cyclohexane with four hydroxyl (OH) groups substituted for hydrogen atoms on four consecutive carbon atoms. Its formula can be written C 6 H 12 O 4, C 6 H 8 (OH)