Fluoroiodomethane: Difference between revisions

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Revision as of 07:22, 3 August 2011

Fluoroiodomethane
Names

IUPAC name Fluoroiodomethane
Other names Fluoro-iodo-methane, Fluoromethyl iodide
Identifiers
CAS Number	373-53-5
3D model (JSmol)	Interactive image
ChemSpider	10329326
ECHA InfoCard	100.201.539
CompTox Dashboard (EPA)	DTXSID00553763
InChI InChI=1S/CH2FI/c2-1-3/h1H2Key: XGVXNTVBGYLJIR-UHFFFAOYSA-N InChI=1/CH2FI/c2-1-3/h1H2
SMILES FCI
Properties
Chemical formula	CH₂FI
Molar mass	159.93 g/mol
Boiling point	53.4 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references

Chemical compound

Fluoroiodomethane is a mixed halomethane, more exactly fluoroiodocarbon (FIC).

Fluoroiodomethane can be prepared from iodoacetic acid.

Its isotopomer 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.

Zheng L.; Berridge M. S. (January 2000). "Synthesis of [F]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. Retrieved 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. Retrieved 2007-06-29.{{cite journal}}: CS1 maint: multiple names: authors list (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)

v t e Halomethanes
Unsubstituted	CH₄
Monosubstituted	CH₃F CH₃Cl CH₃Br CH₃I CH₃At
Disubstituted	CH₂F₂ CH₂ClF CH₂BrF CH₂FI CH₂Cl₂ CH₂BrCl CH₂ClI CH₂Br₂ CH₂BrI CH₂I₂
Trisubstituted	CHF₃ CHClF₂ CHBrF₂ CHF₂I CHCl₂F CHBrClF CHClFI CHBr₂F CHBrFI CHFI₂ CHCl₃ CHBrCl₂ CHCl₂I CHBr₂Cl CHBrClI CHClI₂ CHBr₃ CHBr₂I CHBrI₂ CHI₃
Tetrasubstituted	CF₄ CClF₃ CBrF₃ CF₃I CCl₂F₂ CBrClF₂ CClF₂I CBr₂F₂ CBrF₂I CF₂I₂ CCl₃F CBrCl₂F CCl₂FI CBr₂ClF C*BrClFI CClFI₂ CBr₃F CBr₂FI CBrFI₂ CFI₃ CCl₄ CBrCl₃ CCl₃I CBr₂Cl₂ CBrCl₂I CCl₂I₂ CBr₃Cl CBr₂ClI CBrClI₂ CClI₃ CBr₄ CBr₃I CBr₂I₂ CBrI₃ CI₄
* Chiral compound.

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