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  2. 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.

  3. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    Cyclohexylmethanol is an organic compound with the formula C 6 H 11 −CH 2 −OH. It is a cyclohexane ring functionalized with an alcohol , specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow.

  4. 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'. Acid-catalyzed hydration of this completes the synthesis by forming the tertiary alcohol.

  5. 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).

  6. Alkyl cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Alkyl_cycloalkane

    For instance, a bicyclooctane which consists of a six-member ring and a four-member ring, which share two adjacent carbon atoms which form a shared edge, is [4.2.0]-bicyclooctane. That part of the six-member ring, exclusive of the shared edge has 4 carbons. That part of the four-member ring, exclusive of the shared edge, has 2 carbons.

  7. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Benzene is converted to cyclohexylbenzene by acid-catalyzed alkylation with cyclohexene. [6] Cyclohexylbenzene is a precursor to both phenol and cyclohexanone. [7]Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam.

  8. Cyclohexanehexone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanehexone

    Cyclohexanehexone, also known as hexaketocyclohexane and triquinoyl, is an organic compound with formula C 6 O 6, the sixfold ketone of cyclohexane.It is an oxide of carbon (an oxocarbon), a hexamer of carbon monoxide.

  9. Cyclohexanecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanecarboxylic_acid

    Cyclohexanecarboxylic acid is the organic compound with the formula C 6 H 11 CO 2 H. It is the carboxylic acid of cyclohexane . It is a colorless oil that crystallizes near room temperature.