| Weight | 116.81 g/mol |
|---|---|
| Formula | BF4NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Nitrosonium tetrafluoroborate (14635-75-7)
BF4NO
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LabBot
- Ion radicals. 37. Preparation and isolation of cation radical tetrafluoroborates by the use of nitrosonium tetrafluoroborate (Journal of Organic Chemistry, 1977)
- Desulfurative fluorination using nitrosonium tetrafluoroborate and pyridinium poly(hydrogen fluoride) (Tetrahedron, 1996)
- Aromatic Substitution. XXIII.1 Nitration and Nitrosation of Pyridine with Nitronium and Nitrosonium Tetrafluoroborate. Isolation of N-Nitro- and N-Nitrosopyridinium Tetrafluoroborates (Journal of Organic Chemistry, 1965)
- Electrospray mass spectrometric study of the nature and lability of cationic complexes generated by the reaction of solutions of neutral iron(III), cobalt(III), nickel(II) and copper(II) dithiocarbamates with nitrosonium tetrafluoroborate (Inorganic Chemistry, 1993)
- NITROSATION OF ARYL AND HETEROARYLTRIFLUOROBORATES WITH NITROSONIUM TETRAFLUOROBORATE (Journal of Organic Chemistry, 2012)
- Fluoroaromatics from Arylamines, a Convenient One-Pot Conversion Using Nitrosonium Tetrafluoroborate (Synthetic Communications, 1992)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - BF4NO
-
SMILES[B-](F)(F)(F)F.N#[O+]
-
InChIKeyKGCNVGDHOSFKFT-UHFFFAOYSA-N
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Nitrosonium tetrafluoroborate
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