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2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULPHONATE

2,2,2-Trifluoroethyl Trifluoromethanesulfonate

CAS: 6226-25-1

Molecular Formula: C3H2F6O3S

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2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULPHONATE - Names and Identifiers

Name 2,2,2-Trifluoroethyl Trifluoromethanesulfonate
Synonyms TFOL-TF
2,2,2-TRIFLUOROETHYL TRIFLATE
2,2,2-Trifluoroethyl Trifluoromethanesulfonate
2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULFONATE
2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULPHONATE
2,2,2-trifluoroethyltrifluorometanesulfonicacid
2,2,2-Trifluoroethyl trifluoromethanesulphonate
TRIFLUOROMETHANESULFONIC ACID 2,2,2-TRIFLUOROETHYL ESTER
methanesulfonicacid,trifluoro-,2,2,2-trifluoroethylester
Methanesulfonic acid, 1,1,1-trifluoro-, 2,2,2-trifluoroethyl ester
CAS 6226-25-1
EINECS 458-390-7
InChI InChI=1/C3H2F6O3S/c4-2(5,6)1-12-13(10,11)3(7,8)9/h1H2
InChIKey RTMMSCJWQYWMNK-UHFFFAOYSA-N

2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULPHONATE - Physico-chemical Properties

Molecular FormulaC3H2F6O3S
Molar Mass232.1
Density1,61 g/cm3
Boling Point89-91°C
Flash Point>110°(230°F)
Water SolubilitySlightly soluble in water.
Solubility Chloroform, Methanol (Slightly)
Vapor Presure38.3mmHg at 25°C
AppearanceLiquid
ColorColorless to yellow
Storage Condition2-8°C
SensitiveMoisture Sensitive
Refractive Index1.3037
UseIntermediates in organic synthesis

2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULPHONATE - Risk and Safety

Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R34 - Causes burns
R23/25 - Toxic by inhalation and if swallowed.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDs3265
WGK Germany3
RTECSPB2775000
HS Code29055900
Hazard NoteIrritant
Hazard ClassTOXIC, CORROSIVE
Packing GroupⅡ

2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULPHONATE - Reference Information

EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Application 2,2, 2-trifluoroethyl trifluoromethanesulfonate is a colorless liquid, it can be prepared from trifluoroethanol by an acylation reaction with trifluoroacetic anhydride or trifluoromethanesulfonyl chloride.
preparation in a mL reaction flask, add triethylamine (5.54mL,39.7mmol) and dichloromethane (40mL), the reaction solution was cooled to -25 °c, and then trifluoroacetic anhydride (12.5g,44.3mmol) was added dropwise. After addition, the reaction was continued at -25 °c for 2H, and then trifluoroethanol (2.71g,27.1mmol), and the reaction was stirred at room temperature overnight after the addition was completed. The reaction solution was concentrated under reduced pressure to give crude 2,2, 2-trifluoroethyl triflate as a yellow oily product (6.7g, yield 100%).
Last Update:2024-04-09 20:52:54
2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULPHONATE
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View History
2,2,2-TRIFLUOROETHYL TRIFLUOROMETHANESULPHONATE
2090-05-3
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