| Weight | 70.091 g/mol |
|---|---|
| Formula | C4H6O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Vinyl ether (109-93-3, 9003-19-4)
divinyl ether · divinyl oxide
Score:
#218 in Materials science
,
#1461 in Physics
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#4300 in Chemistry
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- Phospholipids in tissues of the eye I. Isolation, characterization and quantitative analysis by two-dimensional thin-layer chromatography of diacyl and vinyl-ether phospholipids (Biochimica et Biophysica Acta, 1968)
- Living polymerization of isobutyl vinyl ether with hydrogen iodide/iodine initiating system (Macromolecules, 1984)
- Fluorocarbon vinyl ether polymers (1964)
- Time-resolved light scattering studies on kinetics of phase separation and phase dissolution of polymer blends. 1. Kinetics of phase separation of a binary mixture of polystyrene and poly(vinyl methyl ether) (Macromolecules, 1983)
- Preferential surface adsorption in miscible blends of polystyrene and poly(vinyl methyl ether) (Macromolecules, 1988)
- Divinyl Ether Fatty Acid Synthesis in Late BlightDiseased Potato Leaves (The Plant Cell, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - divinyl ether
- divinyl oxide
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SMILESC=COC=C
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- Pubchem - Vinyl ether
- Wikipedia - vinyl ether
Vinyl ether, also known as divinyl ether, divinyl oxide, Vinethene (pharmaceutical trade name) and ethenoxyethene (IUPAC), is a clear, nearly colorless, volatile liquid which was briefly used as an inhalation anesthetic. It can be cyclopolymerized by itself and serves as a cross-linker in copolymerizations. Much to the dismay of some pharmacologists, the synthesis and isolation of pure vinyl ether proved to be a difficult challenge for chemists; vinyl ether was suspected to be a nearly ideal anesthetic as its structure was the combination of an alkene and an ether.
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