| Weight | 164.966 g/mol |
|---|---|
| Formula | C3H4Cl2F2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Methoxyflurane (76-38-0)
Penthrane · Anecotan · Pentrane
Score:
#1173 in Biology
,
#1338 in Chemistry
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- Identification of Cytochrome P450 2E1 as the Predominant Enzyme Catalyzing Human Liver Microsomal Defluorination of Sevoflurane, Isoflurane, and Methoxyflurane (Anesthesiology, 1993)
- Methoxyflurane nephrotoxicity. A study of dose response in man. (JAMA, 1973)
- Human Kidney Methoxyflurane and Sevoflurane Metabolism Intrarenal Fluoride Production as a Possible Mechanism of Methoxyflurane Nephrotoxicity (Anesthesiology, 1994)
- Methoxyflurane metabolism and renal dysfunction: clinical correlation in man. (Anesthesiology, 1971)
- Nephrotoxicity associated with methoxyflurane anesthesia. (Anesthesiology, 1966)
- Minimum Alveolar Concentrations of Methoxyflurane, Halothane, Ether and Cyclopropane in Man: Correlation with Theories of Anesthesia (Anesthesiology, 1967)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Penthrane
- Anecotan
- Pentrane
- Methofluranum
-
SMILESCOC(C(Cl)Cl)(F)F
-
InChIKeyRFKMCNOHBTXSMU-UHFFFAOYSA-N
- Pubchem - Methoxyflurane
- Wikipedia - methoxyflurane
Methoxyflurane (INN), formerly marketed as Penthrane by Abbott Laboratories, is a halogenated ether that was in clinical use as a volatile inhalational anesthetic from its introduction by Joseph F. Artusio et al in 1960 until the late 1970s. It was first synthesized in the late 1940s by William T.
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(383-61-9)
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(354-15-4)
5 alternate names
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44925-09-9
(44925-09-9)
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(354-19-8)
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1,1,2,2-Tetrachloro-1,2-difluoroethane
(76-12-0)
5 alternate names
1 safety hazard
3 suppliers
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(1514-87-0)
5 alternate names
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(90454-18-5, 354-23-4)
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3 suppliers
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(96-34-4)
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7 safety hazards
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(354-25-6)
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(2268-46-4)
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methyl 2,2,2-trifluoroethanimidate
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Methoxyflurane
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