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Fórmula lineal:
CF3SO2OCH3
Número CAS:
Peso molecular:
164.10
UNSPSC Code:
41116105
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-371-7
Beilstein/REAXYS Number:
774772
MDL number:
grade
derivatization grade (GC derivatization)
Quality Segment
assay
≥98.0% (GC), 98.0%
form
liquid
quality
LiChropur™
reaction suitability
reagent type: derivatization reagent
reaction type: Acylations
technique(s)
gas chromatography (GC): suitable
refractive index
n20/D 1.326 (lit.), n20/D 1.327
bp
94-99 °C (lit.)
density
1.45 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
COS(=O)(=O)C(F)(F)F
InChI
1S/C2H3F3O3S/c1-8-9(6,7)2(3,4)5/h1H3
InChI key
OIRDBPQYVWXNSJ-UHFFFAOYSA-N
General description
Shown to be the most effective monomethylating agent in reactions with potassium enolates.
Useful methylation reagent for the conversion of amines to methyl ammonium triflates.
Useful methylation reagent for the conversion of amines to methyl ammonium triflates.
Methyl trifluoromethanesulfonate (Methyl triflate) is a strong methylating agent. It is also a powerful alkylating agent and a strong irritant.
Application
Methyl trifluoromethanesulfonate was used in the synthesis of 2-Benzyloxy-1-methylpyridinium trifluoromethanesulfonate.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
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signalword
Danger
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 3
flash_point_f
100.4 °F - closed cup
flash_point_c
38 °C - closed cup
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W. L. F. Armarego, Christina Li Lin Chai
Purification of Laboratory Chemicals, 189-189 (2013)
Sylwia Ptasińska et al.
The Journal of chemical physics, 135(21), 214309-214309 (2011-12-14)
Gas phase studies of dissociative electron attachment to simple alkyl (CF(3)SO(3)CH(3)) and aryl (C(6)H(5)SO(3)CF(3) and CF(3)SO(3)C(6)H(4)CH(3)) triflates, model molecules of nonionic photoacid generators for modern lithographic applications, were performed. The fragmentation pathways under electron impact below 10 eV were identified
Synthesis, structure, and reactivity of a stabilized phosphiranylium salt.
Helen Jansen et al.
Angewandte Chemie (International ed. in English), 49(32), 5485-5488 (2010-07-06)
Número de artículo de comercio global
| SKU | GTIN |
|---|---|
| 18503-5G | 04061833328422 |
| 18503-1G | 04061826642566 |


