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2 and triethylborane generates the less substituted (and less stable) enolate. After reaction with methyl iodide the former mixture gives 2,2-dimethylcyclohexanone in 90% yield while the latter produces 2,6-dimethylcyclohexanone in 93% yield. [7] [8] The Et stands for ethyl group CH 3 CH 2 −.
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.
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 ...
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 .
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.
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]
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2,5-Hexanedione (Acetonylacetone) is an aliphatic diketone. It is a colorless liquid. [1] In humans, it is a toxic metabolite of hexane and of 2-hexanone.