91741
Trimethylsilyl trifluoromethanesulfonate
purum, ≥98.0% (T)
Synonym(s):
TMS triflate, TMSOTf, Trifluoromethanesulfonic acid trimethylsilylester
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
grade
purum
Quality Level
Assay
≥98.0% (T)
form
liquid
refractive index
n20/D 1.36 (lit.)
bp
77 °C/80 mmHg (lit.)
density
1.228 g/mL at 25 °C (lit.)
SMILES string
C[Si](C)(C)OS(=O)(=O)C(F)(F)F
InChI
1S/C4H9F3O3SSi/c1-12(2,3)10-11(8,9)4(5,6)7/h1-3H3
InChI key
FTVLMFQEYACZNP-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
Trimethylsilyl trifluoromethanesulfonate may be used to catalyze:
- Allylation of acetals to form homoallyl ethers.
- Synthesis of 1,2-trans-glycosides.
- Conversion of alcohols to esters.
- Aminomethylation of silyl enol ethers with aminomethyl alkyl ethers.
- Glycosidation of (+)-4-demethoxyanthracyclinones.
Other Notes
Efficient silylating agent and strong Lewis acid catalyst ; Review
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 3 - Skin Corr. 1B
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
77.0 °F - closed cup
Flash Point(C)
25 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Synthesis of homoallyl ethers via allylation of acetals in ionic liquids catalyzed by trimethylsilyl trifluoromethanesulfonate.
Organic Letters, 5(1), 55-57 (2003)
An extremely fast and efficient acylation reaction of alcohols with acid anhydrides in the presence of trimethylsilyl trifluoromethanesulfonate as catalyst.
Chemical Communications (Cambridge, England), (23), 2625-2626 (1996)
Trimethylsilyl trifluoromethanesulfonate (trimethylsilyl triflate) as an excellent glycosidation reagent for anthracycline synthesis. Simple and efficient synthesis of optically pure 4-demethoxydaunorubicin.
Chemistry Letters (Jpn), 13(4), 501-504 (1984)
J. Prakt. Chem., 341, 410-410 (1999)
Silylating Agents, 2nd ed. (1995)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service