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The resulting cyclohexanecarboxaldehyde is then hydrogenated to give the alcohol. [5] [6] References
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 ...
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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.
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.
Ferrocenecarboxaldehyde behaves like other aldehydes in terms of its reactivity, the main difference is that it is electroactive. Its basicity is indicated by the solubility of the compound in hydrochloric acid.
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'.
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.