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1-Methylcyclohexene. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 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.
Methylcyclohexene. Methylcyclohexene can refer to any of three compounds: 1-Methylcyclohexene. 3-Methylcyclohexene. 4-Methylcyclohexene. set index article chemical compounds. Categories: Set index articles on chemistry. Cyclohexenes.
Cyclohexene is a hydrocarbon with the formula (CH2)4C2H2. It is an example of a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commerical synthesis of nylon.
Methylcyclohexane (cyclohexylmethane) is an organic compound with the molecular formula is CH 3 C 6 H 11. Classified as saturated hydrocarbon, it is a colourless liquid with a faint odor. Methylcyclohexane is used as a solvent. It is mainly converted in naphtha reformers to toluene. [4]
4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 3-methylcyclohexene. All are colorless volatile liquids classified as a cyclic olefins.
Cyclohexanol is the organic compound with the formula HOCH (CH 2) 5. The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group. [4] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature. Millions of tonnes are produced annually ...
C=C1CCCCC1. Properties. Chemical formula. C 7 H 12. Molar mass. 96.170 g/mol. Boiling point. 102 to 103 °C (216 to 217 °F; 375 to 376 K) Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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.