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  2. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    The resulting cyclohexanecarboxaldehyde is then hydrogenated to give the alcohol. [5] [6] References

  3. List of compounds with carbon number 7 - Wikipedia

    en.wikipedia.org/wiki/List_of_compounds_with...

    cyclohexanecarboxaldehyde: 2043-61-0 C 7 H 12 O: dicyclopropyl carbinol: 14300-33-5 C 7 H 12 O: methycyclohexanone: 1331-22-2 C 7 H 12 O 2: cyclohexanecarboxylic acid: 98-89-5 C 7 H 12 O 2: cyclopentaneacetic acid: 1123-00-8 C 7 H 12 O 2: ethyl cyclobutanecarboxylate: 14924-53-9 C 7 H 12 O 2: ethyl tiglate: 5837-78-5 C 7 H 12 O 2 ...

  4. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.

  5. Alkyl cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Alkyl_cycloalkane

    The naming of polycyclic alkanes is more complex, with the base name indicating the number of carbons in the ring system, a prefix indicating the number of rings (e.g., "bicyclo"), and a numeric prefix before that indicating the number of carbons in each part of each ring, exclusive of vertices.

  6. Hydroxyisohexyl 3-cyclohexene carboxaldehyde - Wikipedia

    en.wikipedia.org/?title=Hydroxyisohexyl_3...

    This page was last edited on 23 February 2012, at 18:26 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  7. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 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.

  8. Cyclohexanecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanecarboxylic_acid

    It is prepared by hydrogenation of benzoic acid.. Cyclohexanecarboxylic acid is a precursor to the nylon-6 precursor caprolactam via its reaction with nitrosylsulfuric acid. ...

  9. 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).