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Oxidation of 1-methylcyclohexene catalyzed by cytochrome P450 yields a 2:1 mixture of hydroxylation to epoxidation products. [4] The stereochemistry of hydroformylation has been examined using 1-methylcyclohexene. The main product has the formyl group on the less substituted alkene-carbon, trans with respect to the methyl substituent.
Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44
Methylcyclohexene can refer to any of three compounds: 1-Methylcyclohexene; 3-Methylcyclohexene; 4-Methylcyclohexene This page was last edited on 18 November ...
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]
1-10 minutes, or up to 18 hours Visual disturbance, eye pain, pinpointing of the pupils, runny nose, chest tightness, breathing difficulty, cough, severe nasal congestion, nausea, diarrhea, vomiting, and twitching, VX Gas: colorless Odor: none 1-10 minutes, or up to 42 hours Constricted pupils, visual disturbance, eye pain, runny nose,
This is a list of the various reported boiling points for the elements, with recommended values to be used elsewhere on Wikipedia. ... 13 Al aluminium; use: 2743 K ...
Boiling point: 102 to 103 °C (216 to 217 °F; 375 to 376 K) ... [1] [2] [3] It can also be synthesized as a side product of the dehydration of 2-methylcyclohexanol ...
Benzene is converted to cyclohexylbenzene by acid-catalyzed alkylation with cyclohexene. [6] Cyclohexylbenzene is a precursor to both phenol and cyclohexanone. [7]Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam.