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Tetramethylethylene is an pharmaceutical intermediate. Ozonolysys in neat tetramethyleneethylene gives tetramethyleneethylene epoxide as product.
H. Niki.; P. D. Maker.; C. M. Savage.; L. P. Breitenbach.; M. D. Hurley. FTIR spectroscopic study of the mechanism for the gas-phase reaction between ozone and tetramethylethylene. J. Phys. Chem. 1987, 91 (4),941-946 .
Linus Pauling.; L. O. Brockway. CarbonCarbon Bond Distances. The Electron Diffraction Investigation of Ethane, Propane, Isobutane, Neopentane, Cyclopropane, Cyclopentane, Cyclohexane, Allene, Ethylene, Isobutene, Tetramethylethylene, Mesitylene, and Hexamethylbenzene. Revised Values of Covalent Radii. J. Am. Chem. Soc. 1937, 59 (7),1223-1236 .
Precursor of the sterically hindered hydroborating reagent, "thexylborane", introduced by Brown: J. Am. Chem. Soc., 94, 3561 (1972). For review of its chemistry, see: Synthesis, 77 (1974). This reagent should be freshly prepared since it rearranges on standing to 2,3-dimethyl-1-butylborane.
Gefahrenhinweise (EU): H225-H304
Highly flammable liquid and vapour. May be fatal if swallowed and enters airways.
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves and eye/face protection. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.