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  2. Cyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone

    Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.

  3. File:2-Methylcyclohexanone to 2,2- and 2,6 ...

    en.wikipedia.org/wiki/File:2-Methylcyclohexanone...

    Date: 26 October 2020: Source: Own work based on en:2-Methylcyclohexanone to 2,2- and 2,6-dimethylcyclohexanone.jpg created and asserted as {{PD-chem}} by en:User:EdChem, which they based on "Enoxytriethylborates and Enoxydiethylboranes" in Crich, David , ed. (2008) Reagents for Radical and Radical Ion Chemistry, Handbook of Reagents for Organic Synthesis, 11, John Wiley & Sons ISBN ...

  4. American Metal Market - Wikipedia

    en.wikipedia.org/wiki/American_Metal_Market

    American Metal Market (AMM) is an online provider of industry news and metal pricing information for the U.S. steel, nonferrous and scrap markets. Products include a daily publication available electronically, live news on the publication's website, a hard-copy magazine and a series of weekly newsletters covering niche markets.

  5. Cyclohexenone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexenone

    Cyclohexenone is an organic compound which is a versatile intermediate used in the synthesis of a variety of chemical products such as pharmaceuticals and fragrances. [2] It is colorless liquid, but commercial samples are often yellow. Industrially, cyclohexenone is prepared from phenol by Birch reduction. [3]

  6. Methylcyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexanone

    Methylcyclohexanones are a group of three isomers: 2-methylcyclohexanone, 3-methylcyclohexanone, and 4-methylcyclohexanone. [1] They can be viewed as derivative of cyclohexanone. They can be prepared by oxidation of methylcyclohexane as well as partial hydrogenation of the corresponding cresols. All are colorless liquids. The 2- and 3-isomers ...

  7. 2,5-Dimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2,5-Dimethoxybenzaldehyde

    2,5-Dimethoxybenzaldehyde is an organic compound and a benzaldehyde derivative. One of its uses is the production of 2,5-dimethoxyphenethylamine, also known as 2C-H . 2C-H is used to produce many other substituted phenethylamines such as 2C-B , 2C-I and 2C-C .

  8. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    Most methylcyclohexane is extracted from petroleum but it can be also produced by catalytic hydrogenation of toluene: CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. The hydrocarbon is a minor component of automobile fuel, with its share in US gasoline varying between 0.3 and 1.7% in early 1990s [10] and 0.1 to 1% in 2011. [11]

  9. 2,5-Dimethylhexane - Wikipedia

    en.wikipedia.org/wiki/2,5-Dimethylhexane

    2,5-Dimethylhexane is a branched alkane used in the aviation industry in low revolutions per minute helicopters. [2] As an isomer of octane , the boiling point is very close to that of octane, but can in pure form be slightly lower. 2,5-Dimethylhexane is moderately toxic.

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