| Weight | 72.107 g/mol |
|---|---|
| Formula | C4H8O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
2-Methoxypropene (116-11-0)
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- Catalytic, Enantioselective Acetone Aldol Additions with 2-Methoxypropene (Journal of the American Chemical Society, 1995)
- Improved synthesis of 2-methoxypropene (Journal of Organic Chemistry, 1973)
- The acetonation of lactose and benzyl -lactoside with 2-methoxypropene (Tetrahedron, 1987)
- Synthesis of 2-methoxyallyl chloride, bromide, and iodide by two independent routes. Reaction of N-halosuccinimides with 2-methoxypropene and the pyrolysis of 1-halo-2,2-dimethoxypropanes (Journal of Organic Chemistry, 1972)
- Reaction sof d-lyxose and d-xylose with 2-methoxypropene under kinetic conditions (Carbohydrate Research, 1991)
- INTRAMOLECULAR HOMOLYTIC DISPLACEMENTS. 25. EFFICIENT ACCESS TO EXPOSIDES VIA INDUCED DECOMPOSITION OF UNSATURATED PEROXYKETALS PREPARED BY ADDITION O F A HYDROPEROXIDE TO 2-METHOXYPROPENE (Journal of Organic Chemistry, 1996)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=C)OC
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InChIKeyYOWQWFMSQCOSBA-UHFFFAOYSA-N
- Pubchem - 2-Methoxypropene
- Wikipedia - 2-methoxypropene
2-Methoxypropene is an ether with the chemical formula C4H8O. It is a reagent used in organic synthesis as a protecting group for alcohols, and the converstion diols to the acetonide group. 2-Methoxypropene can be prepared by the elimination of methanol from dimethoxypropane, or by the addition of methanol to propyne or allene.
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