Fluoroiodomethane
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| Fluoroiodomethane | |
|---|---|
| IUPAC name | Fluoroiodomethane |
| Other names | Fluoro-iodo-methane, Fluoromethyl iodide |
| Identifiers | |
| CAS number | [373-53-5] |
| SMILES | C(F)I |
| InChI | 1/CH2FI/c2-1-3/h1H2 |
| Properties | |
| Molecular formula | CH2FI |
| Molar mass | 159.93 g/mol |
| Boiling point |
53.4 °C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
|
Fluoroiodomethane is a mixed halomethane, more exactly fluoroiodocarbon (FIC).
Fluoroiodomethane can be prepared from iodoacetic acid.[1]
Its isotopomer [18F]fluoroiodomethane (PubChem 451313) is a synthetic precursor for fluoromethylation of radiopharmaceuticals.
Also proposal of its use as a safe high-performance foam blowing agent exists.[2]
[edit] See also
[edit] References
- Zheng L.; Berridge M. S. (January 2000). "Synthesis of [18F]fluoromethyl iodide, a synthetic precursor for fluoromethylation of radiopharmaceuticals". Applied Radiation and Isotopes 52 (1): 55–61(7). doi:. PMID 10670923.
- Chin F. T., Morse Ch. L., Shetty H. U., Pike V. W. (December 2005). "Automated radiosynthesis of [18F]SPA-RQ for imaging human brain NK1 receptors with PET". Journal of Labelled Compounds and Radiopharmaceuticals 49 (1): 17–31(15). doi:.
- Tedder, J. M.; Sloan, J. P.; Walton, J. C. (1975). "Free Radical Addition to Olefins, Part XVII. Addition of Fluoroiodomethane to Fluoroethylenes". Journal of the Chemical Society: 1846–1850.

