| Weight | 86.134 g/mol |
|---|---|
| Formula | C5H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
ALLYL ETHYL ETHER (557-31-3)
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- The very low-pressure pyrolysis of phenyl ethyl ether, phenyl allyl ether, and benzyl methyl ether and the enthalpy of formation of the phenoxy radical (International Journal of Chemical Kinetics, 1977)
- Syntheses with perfluoroalkyl iodides. Part II. Addition to non-conjugated alkadienes; cyclization of 1,6-heptadiene, and of 4-substituted 1,6-heptadienoic compounds: bis-allyl ether, ethyl diallylmalonate, N,N-diallylamine and N-substituted diallylamines; and additions to homologous exo- and endocyclic alkenes, and to bicyclic alkenes (Journal of Fluorine Chemistry, 1999)
- Photolysis of organopolysilanes. The reaction of silylenes with allyl ethyl ether (Journal of Organometallic Chemistry, 1983)
- Photolysis of organopolysilanes. Reactions of trimethylsilylphenylsilylene with allylic halides and allyl ethyl ether (Journal of Organometallic Chemistry, 1981)
- A shape memory copolymer based on 2-(dimethylamino)ethyl methacrylate and methyl allyl polyethenoxy ether for potential biological applications (RSC Advances, 2015)
- Reactions of the ethyl radical. Part 9.Addition, dismutation and metathesis with allyl ethyl ether and diallyl ether (Transactions of The Faraday Society, 1969)
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SMILESCCOCC=C
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InChIKeyOJPSFJLSZZTSDF-UHFFFAOYSA-N
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Synthesis
Reactant
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1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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ALLYL ETHYL ETHER
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