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Cyclohexane-1,2-diol is a chemical compound found in castoreum. [1] It can exist in either cis - or trans -isomers . The enzyme cyclohexane-1,2-diol dehydrogenase uses trans -cyclohexane-1,2-diol and NAD + to produce 2-hydroxycyclohexan-1-one , NADH and H + .
1,4-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. This white solid is one of the three isomeric cyclohexanediones . This particular diketone is used as a building block in the synthesis of more complex molecules.
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.
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 ...
1,2-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 is soluble in a variety of organic solvents. It can be prepared by oxidation of cyclohexanone by selenium dioxide. [1] The enol is about 1 kcal/mol more stable than the diketo form. [2]
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An example in the synthesis of trans-cyclohexanediol [6] or by microreactor: [7] A route to synthesizing trans-1,2-diols For academic research and pharmaceutical areas, vicinal diols are often produced from the oxidation of alkenes , usually with dilute acidic potassium permanganate or Osmium tetroxide. [ 8 ]
For eight months, the man had been following the carnivore diet — a high-protein, no-carb plan that focuses on eating only animal products, especially meat, eggs and some dairy; and excludes ...