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flurothyl

Structure via PubChem · Public domain (PubChem)

EntityQ5462894· pop 9· linked from 736 articles

Also known as Indoklon, SK&F-6539, Flurotyl, HFE-356mff2

Flurothyl (formerly under the trade name Indoklon) (IUPAC names: 1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane or bis(2,2,2-trifluoroethyl) ether) is a volatile liquid drug from the halogenated ether family, related to inhaled anaesthetic agents such as diethyl ether and sevoflurane, but having the opposite effects, acting as a stimulant and convulsant. A clear and stable liquid, it has a mild ethereal odor whose vapors are non-flammable. It is excreted from the body by the lungs in an unchanged state.

Chemical data

Formula
C4H4F6O
Molecular weight
182.06 g/mol
IUPAC name
1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane
SMILES
C(C(F)(F)F)OCC(F)(F)F
InChIKey
KGPPDNUWZNWPSI-UHFFFAOYSA-N
XLogP
2.3
Polar surface area
9.2 Ų
H-bond donors
0
H-bond acceptors
7
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
182.017
Has use
medication
Show 4 more facts
chemical formula
C₄H₄F₆O
canonical SMILES
C(C(F)(F)F)OCC(F)(F)F
Commons category
Flurothyl
global warming potential
20
Sources (2)

via Wikidata · CC0

~5 min read

Encyclopedic overview

4 sections
Contents
  • Research into psychiatric treatment
  • Mechanism of action
  • See also
  • References

Flurothyl (formerly under the trade name Indoklon) (IUPAC names: 1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane or bis(2,2,2-trifluoroethyl) ether) is a volatile liquid drug from the halogenated ether family, related to inhaled anaesthetic agents such as diethyl ether and sevoflurane, but having the opposite effects, acting as a stimulant and convulsant. A clear and stable liquid, it has a mild ethereal odor whose vapors are non-flammable. It is excreted from the body by the lungs in an unchanged state.

Several compounds related to the halogenated ether anesthetics have similar convulsant effects rather than producing sedation, and this has been helpful in studying the mechanism of action of these drugs.

Excerpted from Wikipedia’s “flurothyl” article, available under the CC BY-SA 4.0 licence.

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