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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. 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. ...

  4. 1,4-Cyclohexanedicarboxylic acid - Wikipedia

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

    1,4-Cyclohexanedicarboxylic acid describes a pair of organic compounds with the formula C 6 H 10 (CO 2 H) 2.The CO 2 H groups are attached to the opposite carbon centers of the cyclohexane ring.

  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. TV2 (Hungarian TV channel) - Wikipedia

    en.wikipedia.org/wiki/TV2_(Hungarian_TV_channel)

    TV2 (TV Kettő) is a Hungarian free-to-air television channel operating since 4 October 1997, providing a large variety of programming. It is a competitor with RTL for the first place in Hungarian television ratings.

  7. 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.

  8. Hydroxymethylpentylcyclohexenecarboxaldehyde - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethylpentylcyclo...

    Typical synthesis starts from myrcene [2] and involves a Diels–Alder reaction with acrolein to produce the cyclohexenecarbaldehyde group, this species is marketed as a fragrance in its own right, most commonly under the name 'myrac aldehyde'.

  9. 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.

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