Weight | 126.077 g/mol |
---|---|
Formula | C4H5F3O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
FLUROXENE (406-90-6)
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- Equipotent Alveolar Concentrations of Methoxyflurane, Halothane, Diethyl Ether, Fluroxene, Cyclopropane, Xenon and Nitrous Oxide in the Dog (Anesthesiology, 1965)
- Minimum alveolar concentrations in man on awakening from methoxyflurane, halothane, ether and fluroxene anesthesia: MAC awake. (Anesthesiology, 1970)
- Comparison of the Arrhythmic Doses of Epinephrine during Forane, Halothane, and Fluroxene Anesthesia in Dogs (Anesthesiology, 1971)
- Destruction of cytochrome P-450 by vinyl fluoride, fluroxene, and acetylene. Evidence for a radical intermediate in olefin oxidation (Biochemistry, 1982)
- The effects of halothane, fluroxene and cyclopropane on ventilation: a comparative study in man. (Anesthesiology, 1966)
- ELECTROENCEPHALOGRAPHIC SEIZURE ACTIVITY IN DOGS DURING ANAESTHESIA Studies with Ethrane, fluroxene, halothane, chloroform, divinyl ether, diethyl ether, methoxyflurane, cyclopropane and Forane (BJA: British Journal of Anaesthesia, 1971)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=COCC(F)(F)F
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InChIKeyDLEGDLSLRSOURQ-UHFFFAOYSA-N
- Pubchem - FLUROXENE
- Wikipedia - fluroxene
Fluroxene (INN, USAN; brand name Fluoromar), or 2,2,2-trifluoroethyl vinyl ether, is a volatile, inhalational anesthetic, and was the first halogenated hydrocarbon anesthetic to be introduced. It was synthesized in 1951, and was introduced for clinical use in 1954, but was voluntarily withdrawn from the market in 1974 due to its potential flammability and accumulating evidence that it could cause organ toxicity. In any case, prior to being discontinued, it had largely been superseded by halothane.
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