Chlorofluorodiiodomethane

Chlorofluorodiiodomethane
Names
	Preferred IUPAC name Сhloro-fluoro-diiodomethane
	Other names Chloro(fluoro)diiodomethane
Identifiers
CAS Number	1495-15-4 ;
3D model (JSmol)	Interactive image;
ChemSpider	24590927;
PubChem CID	85696063;
	InChI InChI=1S/CClFI2/c2-1(3,4)5 Key: KRMKVMPRGWVUNY-UHFFFAOYSA-N;
	SMILES C(F)(Cl)(I)I;
Properties
Chemical formula	CClFI2
Molar mass	320.27 g·mol−1
Density	3.2±0.1 g/cm³
Boiling point	148.1 °C (298.6 °F; 421.2 K)
Hazards
Flash point	43.4±18.4 °C
Related compounds
Related compounds	Bromofluoroiodomethane; Dibromofluoroiodomethane; Bromodifluoroiodomethane; Chlorofluoroiodomethane; Chlorodifluoroiodomethane;
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Chlorofluorodiiodomethane is a tetrahalomethane with the chemical formula CClFI₂.^[1] This is an organic compound containing two iodine atoms, one chlorine atom, and one fluorine atom attached to the methane backbone. Some sources claim that the compound still expects isolation.^[2]^[3]

References

^ Frenkel, Michael; Kabo, G. J.; Marsh, K. N.; Roganov, G. N.; Wilhoit, R. C. (15 June 1994). Thermodynamics of Organic Compounds in the Gas State. CRC Press. p. 738. ISBN 978-1-883400-04-0. Retrieved 9 November 2025.
^ Katritzky, Alan R.; Gilchrist, Thomas L.; Meth-Cohn, Otto; Rees, Charles Wayne (21 March 2003). Comprehensive Organic Functional Group Transformations. Elsevier. p. 228. ISBN 978-0-08-042704-1. Retrieved 9 November 2025.
^ Taylor, John B.; Triggle, David J. (2007). Comprehensive Medicinal Chemistry II. Elsevier. p. 2193. ISBN 978-0-08-044513-7. Retrieved 9 November 2025.

[1] Frenkel, Michael; Kabo, G. J.; Marsh, K. N.; Roganov, G. N.; Wilhoit, R. C. (15 June 1994). Thermodynamics of Organic Compounds in the Gas State. CRC Press. p. 738. ISBN 978-1-883400-04-0. Retrieved 9 November 2025.

[2] Katritzky, Alan R.; Gilchrist, Thomas L.; Meth-Cohn, Otto; Rees, Charles Wayne (21 March 2003). Comprehensive Organic Functional Group Transformations. Elsevier. p. 228. ISBN 978-0-08-042704-1. Retrieved 9 November 2025.

[3] Taylor, John B.; Triggle, David J. (2007). Comprehensive Medicinal Chemistry II. Elsevier. p. 2193. ISBN 978-0-08-044513-7. Retrieved 9 November 2025.

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