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Methyl trifluoromethanesulfonate

Catalog Number
ACM333277
CAS Number
333-27-7
Product Name
Methyl trifluoromethanesulfonate
Structure
Category
Other Electronic Materials
Synonyms
methyl-triflate; EINECS 206-371-7; Trifluoromethanesulfonic Acid Methyl Ester; Methyltrifluoromethanesulfonate; Methyl Trifluoromethanesulfonate; trifluoromethanesulphonic acid methyl ester; Methyl triflate; Methanesulfonic acid,trifluoro-,methyl ester; Methyl trifluoromethane sulfonate; Methyl trifluoromethanesulphonate;
IUPAC Name
methyltrifluoromethanesulfonate
Molecular Weight
164.1
Molecular Formula
C2H3F3O3S
Canonical SMILES
COS(=O)(=O)C(F)(F)F
InChI Key
OIRDBPQYVWXNSJ-UHFFFAOYSA-N
Boiling Point
95ºC
Flash Point
38ºC
Purity
97%
Density
1.45
Appearance
Colourless Liquid
Application
Methyl trifluoromethanesulfonate, appearing as a clear colorless to yellow liquid, serves as a powerful and versatile reagent in chemical synthesis. Its primary purpose lies in its role as a methylating agent, efficiently facilitating the conversion of amines to methyl ammonium triflates. In addition to its methylation capabilities, this compound is employed in acylation reactions as a derivatization reagent. It is key in the pre-methylation of polysaccharides under mild basic conditions, contributing to methods for determining polysulfide species such as zerovalent sulfur and polysulfides in environments like sulfide-rich water wells and lithium-sulfur battery electrolytes using chromatography-based techniques. Furthermore, methyl trifluoromethanesulfonate is also utilized in reactions with potassium enolates and the synthesis of 2-Benzyloxy-1-methylpyridinium trifluoromethanesulfonate, as well as in the Suzuki reaction, highlighting its broad applicability in chemical research and industry.
EC Number
206-371-7
Exact Mass
163.97500
Hazard Statements
C:Corrosive;
Safety Description
S16-S26-S36/37/39-S45
Stability
Stable under normal temperatures and pressures.
UN Number
2924
WGK Germany
3
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