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2. 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.

3. Cyclohexene - Wikipedia

   en.wikipedia.org/wiki/Cyclohexene

   Cyclohexene is a hydrocarbon with the formula (CH 2) 4 C 2 H 2. It is a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon. [3]

4. Hagemann's ester - Wikipedia

   en.wikipedia.org/wiki/Hagemann's_ester

   Hagemann's ester, ethyl 2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist Carl Hagemann. The compound is used in organic chemistry as a reagent in the synthesis of many natural products including sterols , trisporic acids , and terpenoids .

5. Cyclohexanol - Wikipedia

   en.wikipedia.org/wiki/Cyclohexanol

   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. The oxidation involves radicals and the intermediacy of the hydroperoxide C 6 H 11 O 2 H. Alternatively, cyclohexanol can be produced by the hydrogenation of phenol ...

6. 2-(2-(4-Methyl-3-cyclohexen-1-yl)propyl)cyclopentanone ...

   en.wikipedia.org/wiki/2-(2-(4-Methyl-3...

   2-[2-(4-Methyl-3-cyclohexen-1-yl)propyl]cyclopentanone (trade name by Givaudan: Nectaryl) is an organic compound belonging to the group of ketones and cycloalkanes. The compound is used as a fragrance .

7. 1,3-Cyclohexanedione - Wikipedia

   en.wikipedia.org/wiki/1,3-Cyclohexanedione

   1,3-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. It is one of three isomeric cyclohexanediones. It is a colorless compound that occurs naturally. It is the substrate for cyclohexanedione hydrolase. The compound exists mainly as the enol tautomer. [2]