enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Cyclohexane-1,2,3,4,5,6-hexol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane-1,2,3,4,5,6-hexol

    Cyclohexane-1,2,3,4,5,6-hexol is a family of chemical compounds with formula C 6 H 12 O 6, whose molecule consists of a ring of six carbon atoms, each bound to one hydrogen atom and one hydroxyl group (–OH). There are nine stereoisomers, that differ by the position of the hydroxyl groups relative to the mean plane of the ring.

  3. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    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] Cyclohexyl (C 6 H 11) is the alkyl substituent of cyclohexane and is ...

  4. 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.

  5. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    A monosubstituted cyclohexane is one in which there is one non-hydrogen substituent in the cyclohexane ring. The most energetically favorable conformation for a monosubstituted cyclohexane is the chair conformation with the non-hydrogen substituent in the equatorial position because it prevents high steric strain from 1,3 diaxial interactions. [10]

  6. 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.

  7. 1,4-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,4-Cyclohexanedione

    Names Preferred IUPAC name. Cyclohexane-1,4-dione. Identifiers CAS Number. 637-88-7 3D model . Interactive image; 3DMet B01109; Beilstein Reference. 774152 ChEBI:

  8. 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 ...

  9. Nitrocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Nitrocyclohexane

    Names IUPAC name. Nitrocyclohexane ... CAS Number. 1122-60-7 3D model . Interactive image; ChemSpider: 13647; ECHA InfoCard ... Cyclohexane is a convenient substrate ...