| Weight | 283.324 g/mol |
|---|---|
| Formula | C13H14FNO3S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
58086-67-2 (58086-67-2)
2-fluoro-1-methylpyridinium tosylate · 2-fluoro-1-methylpyridinium iodide · 2-fluoro-1-methylpyridinium
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- Hydrolyses of 2- and 4-fluoro N-heterocycles. II: Nucleophilic catalysis by buffer bases in the hydrolysis of 2-fluoro-1-methylpyridinium iodide (Journal of Organic Chemistry, 1987)
- OXIDATION OF ALCOHOLS WITH 2-FLUORO-1-METHYLPYRIDINIUM TOSYLATE AND DIMETHYL SULFOXIDE OR HEXAMETHYLENETETRAMINE (Chemistry Letters, 1978)
- Hydrolyses of 2- and 4-fluoro N-heterocycles. 4. Proton inventories of the hydrolyses of 2-fluoro-1-methylpyridinium iodide, 4-fluoroquinaldine, and 2-chloro-1-methylpyrimidinium triflate (Journal of Organic Chemistry, 1992)
- ChemInform Abstract: OXIDATION OF ALCOHOLS WITH 2-FLUORO-1-METHYLPYRIDINIUM TOSYLATE AND DIMETHYL SULFOXIDE OR HEXAMETHYLENETETRAMINE (ChemInform, 1978)
- ChemInform Abstract: Cyclopropane-Ring Formation from Trialkylstannyl Alcohols by Using 2-Fluoro-1-methylpyridinium Tosylate. (ChemInform, 1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-fluoro-1-methylpyridinium tosylate
- 2-fluoro-1-methylpyridinium iodide
- 2-fluoro-1-methylpyridinium
-
SMILESCC1=CC=C(C=C1)S(=O)(=O)[O-].C[N+]1=CC=CC=C1F
-
InChIKeyHQWDKLAIDBOLFE-UHFFFAOYSA-M
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