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  2. 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 ...

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple ...

  4. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    An example of a common name is terpineol, the name of which can tell us only that it is an alcohol (because the suffix "-ol" is in the name) and it should then have a hydroxyl group (–OH) attached to it. The IUPAC naming system for organic compounds can be demonstrated using the example provided in the adjacent image.

  5. 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.

  6. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    Names Preferred IUPAC name. Cyclohexylmethanol. Other names ... It is a cyclohexane ring functionalized with an alcohol, specifically a hydroxymethyl group. The ...

  7. Cyclohexanecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanecarboxylic_acid

    Names Preferred IUPAC name. ... It is the carboxylic acid of cyclohexane. It is a colorless oil that crystallizes near room temperature. [2] Preparation and reactions

  8. Cyclohexanethiol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanethiol

    Names Preferred IUPAC name. Cyclohexanethiol. ... It was first prepared by the free-radical reaction of cyclohexane using carbon disulfide as a sulfur source. [1]

  9. Cyclohexane (data page) - Wikipedia

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

    The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source and follow its directions.