Weight | 184.491 g/mol |
---|---|
Formula | C3H2ClF5O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
Enflurane (13838-16-9)
Ethrane · Enfran · Alyrane
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- Biotransformation of halothane, enflurane, isoflurane, and desflurane to trifluoroacetylated liver proteins: association between protein acylation and hepatic injury. (Anesthesia & Analgesia, 1997)
- A comparative interaction of epinephrine with enflurane, isoflurane, and halothane in man. (Anesthesia & Analgesia, 1976)
- Airway irritation produced by volatile anaesthetics during brief inhalation: comparison of halothane, enflurane, isoflurane and sevoflurane (Canadian Journal of Anaesthesia-journal Canadien D Anesthesie, 1993)
- The Effects of Sevoflurane, Halothane, Enflurane, and Isoflurane on Hepatic Blood Flow and Oxygenation in Chronically Instrumented Greyhound Dogs (Anesthesiology, 1992)
- Carbon Monoxide Production from Degradation of Desflurane, Enflurane, Isoflurane, Halothane, and Sevoflurane by Soda Lime and Baralyme@ (Anesthesia & Analgesia, 1995)
- The Anesthetic Potency of Fentanyl in Terms of Its Reduction of Enflurane MAC (Anesthesiology, 1982)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - H361: Suspected of damaging fertility or the unborn child
Warning Reproductive toxicity - Category 2 - Ethrane
- Enfran
- Alyrane
- Enlirane
- Etran
-
SMILESC(C(OC(F)F)(F)F)(F)Cl
-
InChIKeyJPGQOUSTVILISH-UHFFFAOYSA-N
- Pubchem - Enflurane
- Wikipedia - enflurane
Enflurane (2-chloro-1,1,2,-trifluoroethyl-difluoromethyl ether) is a halogenated ether. Developed by Ross Terrell in 1963, it was first used clinically in 1966. It was increasingly used for inhalational anesthesia during the 1970s and 1980s but is no longer in common use.
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Similar Compounds
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14620-81-6
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(76-15-3)
6 alternate names
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3 suppliers
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