| Weight | 161.211 g/mol |
|---|---|
| Formula | C6H18F3N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Triethylamine trihydrofluoride (73602-61-6)
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- Removal of f-butyldimethylsilyl protection in RNA-synthesis. Triethylamine trihydrofluoride (TEA, 3HF) is a more reliable alternative to tetrabutylammonium fluoride (TBAF) (Nucleic Acids Research, 1994)
- Microwave-assisted aliphatic fluorinechlorine exchange using triethylamine trihydrofluoride (TREAT-HF) (Tetrahedron Letters, 2009)
- A convenient procedure for the deprotection of silylated nucleosides and nucleotides using triethylamine trihydrofluoride (Bioorganic & Medicinal Chemistry Letters, 1994)
- Improved synthesis of 9-(2,3-dideoxy-2-fluoro--d-threo-pentofuranosyl)adenine (FddA) using triethylamine trihydrofluoride (Tetrahedron Letters, 2001)
- Voltammetric behavior of triethylamine trihydrofluoride and anisole in acetonitrile as a first approach of studies for electro-fluorination of some adducts (Electrochimica Acta, 2012)
- ChemInform Abstract: Improved Synthesis of 9-(2,3-Dideoxy-2-fluoro--D-threo-pentofuranosyl)adenine (FddA) Using Triethylamine Trihydrofluoride. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCN(CC)CC.F.F.F
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InChIKeyIKGLACJFEHSFNN-UHFFFAOYSA-N
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