Ad
related to: cyclohexene oxide msds sheet price
Search results
Results from the WOW.Com Content Network
Cyclohexene oxide is produced in epoxidation reaction from cyclohexene. The epoxidation can take place either in a homogeneous reaction by peracids [2] or heterogeneous catalysis (e.g. silver and molecular oxygen). [3] [4] [5]
4-Vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4-position of the cyclohexene ring. It is a colorless liquid. Although chiral, it is used mainly as the racemate. It is a precursor to vinylcyclohexene dioxide. [4]
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.
1-Methylcyclohexene an organic compound consisting of cyclohexene with a methyl group substituent attached to the alkene group. Two other structural isomers are known: 3-methylcyclohexene and 4-methylcyclohexene. All are colorless volatile liquids. They are specialized reagents.
1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. 4 Vapor pressure of liquid. 5 Distillation data. 6 Spectral data. 7 References.
Most methylcyclohexane is extracted from petroleum but it can be also produced by catalytic hydrogenation of toluene: CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. The hydrocarbon is a minor component of automobile fuel, with its share in US gasoline varying between 0.3 and 1.7% in early 1990s [10] and 0.1 to 1% in 2011. [11]
4-Vinylcyclohexene dioxide, like other volatile epoxides, is classified as an alkylating agent. [5] VCD has toxic effects on fertility. It is a killer of oocytes, eggs in a female's ovaries, in immature ovarian follicles in mice and rats.
This page was last edited on 18 November 2024, at 14:45 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Ad
related to: cyclohexene oxide msds sheet price