Ad
related to: 2 cyclohexen 1 one sds solutionuline.com has been visited by 1M+ users in the past month
Search results
Results From The WOW.Com Content Network
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.
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]
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 ...
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 .
2-Hydroxy-3-methyl-2-cyclopenten-1-one is an organic compound related to 1,2-cyclopentanedione. It is the enol tautomer of the diketone 3-methylcyclopentane-1,2-dione. Being an enol, the compound is often called methylcyclopentenolone. It is a colorless solid.
In the presence of a Cinchona alkaloid, bromination of an alkene can leads to optically active dibromides. [2] For 4-methylcyclohexene, the ( S )-configuration leads to two different products: the bromines can add at the axial positions, giving the orientation (1 S ,3 R ,4 R ), or at the equatorial positions, giving the orientation (1 S ,3 S ,4 ...
Cyclohexylmethanol is an organic compound with the formula C 6 H 11 −CH 2 −OH. It is a cyclohexane ring functionalized with an alcohol , specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow.
In contrast to that, the other stereo isomers show an unspecific fruity odor, the odor detection threshold are 11.2 ng·l −1 and 14.9 ng·l −1 which is much higher. [ 2 ] [ 3 ] The tenacity on blotter , the time during which the compound is smellable with unchanged characteristics, [ 4 ] : 51 is reported to be three weeks.