2,2,2-Trifluoroethyl vinyl ether

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2,2,2-Trifluoroethyl vinyl ether Basic information
Product Name:2,2,2-Trifluoroethyl vinyl ether
Synonyms:fluoroxene;fluorxene;trifluoroethylvinylether;2,2,2-TRIFLUOROETHYL VINYL ETHER, 97%, STAB. WITH 0.1% TRIET;2,2,2-Trifluoroethyl vinyl ether, 97%, stab.;Fluroxen;(2,2,2-Trifluoroethoxy)ethene, Fluoroxene;fluoromar
CAS:406-90-6
MF:C4H5F3O
MW:126.08
EINECS:206-977-1
Product Categories:CARDIZEM
Mol File:406-90-6.mol
2,2,2-Trifluoroethyl vinyl ether Structure
2,2,2-Trifluoroethyl vinyl ether Chemical Properties
Boiling point 42-43°C
density 1,135 g/cm3
refractive index 1.3192
Fp -30°C
storage temp. 2-8°C
form A liquid
Water Solubility 4mg/L(temperature not stated)
Merck 14,4202
BRN 1745876
Henry's Law Constant5.4×10-4 mol/(m3Pa) at 25℃, Fogg and Sangster (2003)
Exposure limitsNIOSH: Ceiling 2 ppm(10.3 mg/m3)
InChIInChI=1S/C4H5F3O/c1-2-8-3-4(5,6)7/h2H,1,3H2
InChIKeyDLEGDLSLRSOURQ-UHFFFAOYSA-N
SMILESC=COCC(F)(F)F
CAS DataBase Reference406-90-6(CAS DataBase Reference)
EPA Substance Registry SystemEthene, (2,2,2-trifluoroethoxy)- (406-90-6)
Safety Information
Hazard Codes F,Xi
Risk Statements 11-41-10
Safety Statements 16-36-39-26
RIDADR 1993
OELCeiling: 2 ppm (10.3 mg/m3) [60-minute] [*Note: REL for exposure to waste anesthetic gas.]
RTECS KO4250000
Hazard Note Flammable
TSCA TSCA listed
HazardClass 3
PackingGroup II
HS Code 2909199090
Toxicitymmo-sat 3 pph/2H MUREAV 58,183,78
MSDS Information
ProviderLanguage
ALFA English
2,2,2-Trifluoroethyl vinyl ether Usage And Synthesis
DescriptionFluroxene , 2,2,2-trifluoro-1- vinyloxyethane, is a colorless liquid with a pungent odor. It is inflammable and, at concentrations above 4 %, explosive in air. Fluroxene (MAC3.4) generally is used in a mixture with oxygen and nitrous oxide. Several cases of liver damage have been observed.
OriginatorFluoromar, Ohio Medical, US ,1961
UsesCa channel blocker, coronary vasodilator
DefinitionChEBI: Fluroxene is an organofluorine compound.
Manufacturing ProcessThe following process description is taken from US Patent 2,830,007.
270 grams 2,2,2-trifluoroethanol was added slowly to 15 grams of a cooled suspension of potassium metal in 250 ml of ethyl ether with stirring. When all the potassium metal had reacted, the resulting solution was fractionally distilled in order to remove the ethyl ether. The residue was placed in a bomb and the air was removed from the bomb by flushing with acetylene. The bomb was sealed and heated to 150°C. Acetylene was then introduced at 245 to 260 psi and the gas pressure was maintained for a period of 5 hours under mechanical agitation throughout the reaction. At the end of this time, heating was discontinued, the flow of acetylene was shut off and the bomb was allowed to cool to room temperature. The excess pressure in the bomb was reduced to atmospheric pressure by venting any gases through a dry ice cooled trap.
The reaction mixture comprising 2,2,2-trifluoroethyl vinyl ether, 2.2.2trifluoroethanol and potassium 2,2,2-trifluoroethylate was fractionally distilled, whereupon crude 2,2,2-trifluoroethyl vinyl ether was obtained which boiled at 42° to 45°C at 760 mm. More 2,2,2-trifluoroethyl vinyl ether was obtained when the distillation residue was returned to the bomb and reacted with acetylene in the same manner as hereinabove described.
The alkali metal hydroxides, instead of the alkali metals per se, can be employed to produce the alkali metal 2,2,2-trifluoroethanolate. However, this introduces water in the reaction mixture which requires removal prior to vinylation with acetylene. The crude products, on further distillation, yielded 2,2,2-trifluoroethyl vinyl ether having a boiling point of 43.1°C at 759 mm.
Therapeutic FunctionInhalation anesthetic
General DescriptionVolatile Liquid. Bp: 43°C. Density: 1.14 g cm-3 . Formerly used as an inhalation anesthetic.
Reactivity Profile2,2,2-TRIFLUOROETHYL VINYL ETHER is non-flammable but combustible. Can form explosive mixtures with air. Reacts with strong oxidizing agents.
Safety ProfilePoison by inhalation. Moderately toxic by intraperitoneal route. An experimental teratogen. Human systemic effects by inhalation: jaundice and liver function tests impaired. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of F-. Used as an anesthetic. See also FLUORIDES and ETHERS.
SynthesisThe compound is prepared by catalytic vinylation of 2,2,2-trifluoroethanol in the presence of alkali-metal trifluoroethoxide :
Synthesis_406-90-6
2,2,2-Trifluoroethyl vinyl ether Preparation Products And Raw materials
Raw materialsPotassium-->Acetylene
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