| Weight | 147.908 g/mol |
|---|---|
| Formula | C3H9BF4O |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Trimethyloxonium tetrafluoroborate (420-37-1)
trimethyloxonium tetrafluoroborate(1-) · TMOTFB
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- A direct and mild conversion of tertiary aryl amides to methyl esters using trimethyloxonium tetrafluoroborate: A very useful complement to directed metalation reactions (Tetrahedron, 2000)
- Determination of organic acids in urine by solidphase microextraction and gas chromatographyion trap tandem mass spectrometry previous in sample derivatization with trimethyloxonium tetrafluoroborate (Biomedical Chromatography, 2008)
- Profiling of organic acids by capillary gas chromatographymass spectrometry after direct methylation in urine using trimethyloxonium tetrafluoroborate (Journal of Chromatography A, 1999)
- Reactions of trimethyloxonium tetrafluoroborate and dihalo-bis-ligandplatinum(II) complexes (Inorganica Chimica Acta, 1972)
- Chemistry of low-valent metal isocyanide complexes. Part 2. Oxidative reactions of pentakis(t-butyl isocyanide)iron with alkyl, allyl, benzyl, fluoroalkyl, and pentafluorophenyl halides, and with trimethyloxonium tetrafluoroborate and diphenylacetylene. Evidence for isocyanide insertion reactions, and the molecular structure of [Fe(CNBut)3{14--C(NBut)C(Ph)C(Ph)C(NBut)}] (Journal of The Chemical Society-dalton Transactions, 1980)
- Esterification of Hemins with Trimethyloxonium Tetrafluoroborate (Analytical Biochemistry, 1976)
- trimethyloxonium tetrafluoroborate(1-)
- TMOTFB
-
SMILES[B-](F)(F)(F)F.C[O+](C)C
-
InChIKeyCZVZBKHWOFJNCR-UHFFFAOYSA-N
- Pubchem - Trimethyloxonium tetrafluoroborate
- Wikipedia - Trimethyloxonium tetrafluoroborate
Trimethyloxonium tetrafluoroborate is the organic compound with the formula Me3OBF4. It is sometimes called the "Meerwein salt" after Hans Meerwein.) This salt is a strong methylating agent, being a source of CH3+. It is a white solid.
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Trimethyloxonium tetrafluoroborate
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