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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. 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. ...

  7. Heteroatom-promoted lateral lithiation - Wikipedia

    en.wikipedia.org/wiki/Heteroatom-promoted...

    The reaction mixture was cooled to 0°, treated with cyclohexanecarboxaldehyde (4.2 mL, 35 mmol), allowed to warm to ambient temperature again, and poured into saturated aqueous ammonium chloride solution. The mixture was extracted with ether and the ether extract was washed with water and brine and concentrated in vacuo.

  8. Hydroformylation - Wikipedia

    en.wikipedia.org/wiki/Hydroformylation

    Hydroformylation of an alkene (R 1 to R 3 organyl groups (i. e. alkyl-or aryl group) or hydrogen). In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes (R−CH=O) from alkenes (R 2 C=CR 2).

  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.