Fluoroiodomethane
Itsura
| Mga pangalan | |
|---|---|
| Pangalang IUPAC
Fluoroiodomethane | |
| Mga ibang pangalan
Fluoro-iodo-methane, Fluoromethyl iodide | |
| Mga pangkilala | |
Modelong 3D (JSmol) |
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| ChemSpider | |
| Infocard ng ECHA | 100.201.539 |
Dashboard ng CompTox (EPA) |
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| Mga pag-aaring katangian | |
| CH2FI | |
| Bigat ng molar | 159.93 g/mol |
| Puntong kumukulo | 53.4 °C |
Maliban kung saan nabanggit, binigay ang datos para sa mga materyales sa kanilang estadong pamantayan (sa 25 °C [77 °F], 100 kPa).
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Ang Fluoroiodomethane ay pinaghalong halomethane, pinakasakto bilang fluoroiodocarbon (FIC).
Ang Fluoroiodomethane ay maaaring ihanda mula sa iodoacetic acid.[1]
Ang kanyang isotopomer [18F]fluoroiodomethane (PubChem 451313) ay isang sintetikong pinanggalingan mula sa fluoromethylation ng radiopharmaceuticals.
Talababa
[baguhin | baguhin ang wikitext]Mga Sanggunian
[baguhin | baguhin ang wikitext]- 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:10.1016/S0969-8043(99)00061-5. PMID 10670923. Nakuha noong 2007-06-29.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - 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:10.1002/jlcr.1016. Nakuha noong 2007-06-29.
{{cite journal}}: CS1 maint: multiple names: authors list (link)[patay na link] - 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.
{{cite journal}}: CS1 maint: multiple names: authors list (link)