Fluoroiodomethane
Names | |
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Preferred IUPAC name
Fluoro(iodo)methane | |
Other names
Fluoroiodomethane
Fluoro-iodo-methane Fluoromethyl iodide | |
Identifiers | |
3D model (
JSmol ) |
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ChemSpider | |
ECHA InfoCard
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100.201.539 |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
CH2FI | |
Molar mass | 159.93 g/mol |
Boiling point | 53.4 °C (128.1 °F; 326.5 K) |
Hazards | |
GHS labelling: | |
Danger | |
H301, H311, H330 | |
P260, P264, P270, P271, P280, P284, P301+P310, P302+P352, P304+P340, P310, P312, P320, P321, P322, P330, P361, P363, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Fluoroiodomethane is the halomethane with the formula FCH2I. Also classified as a fluoroiodocarbon (FIC), it is a colorless liquid. It is a reagent for the introduction of the fluoromethyl (FCH2) group.
Synthesis and uses
It is prepared by fluorination of
methylene iodide.[1]
Its
radiopharmaceuticals
.
Additional reading
- 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). 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). ]
- 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.
References
- ISBN 978-0471936237.