Weight | 195.909 g/mol |
---|---|
Formula | CF3I |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Trifluoromethyl iodide (2314-97-8)
trifluoroiodomethane · C-F3-I · iodotrifluoromethane
Score:
#2084 in Physics
,
#6482 in Chemistry
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- Preparation of trifluoromethyl aryl sulfides using Silver(I) trifluoromethanethiolate and an inorganic iodide (Journal of Organic Chemistry, 2000)
- THE MICROWAVE SPECTRA AND MOLECULAR STRUCTURES OF TRIFLUOROMETHYL BROMIDE, IODIDE, AND CYANIDE (Journal of Chemical Physics, 1952)
- Nucleophilic trifluoromethylation using trifluoromethyl iodide. A new and simple alternative for the trifluoromethylation of aldehydes and ketones. (Organic Letters, 2001)
- Tetrakis(dimethylamino)ethylene/trifluoroiodomethane. a specific novel trifluoromethylating agent (Journal of Fluorine Chemistry, 1989)
- Absolute integrated infrared absorption intensities of trichlorofluoromethane and trifluoroiodomethane fundamentals in the gas phase. Intensity sum rule (The Journal of Physical Chemistry, 1975)
- Nucleophilic trifluoromethylation of acyl chlorides using the trifluoromethyl iodide/TDAE reagent (Tetrahedron Letters, 2002)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H341: Suspected of causing genetic defects
Warning Germ cell mutagenicity - Category 2 - trifluoroiodomethane
- C-F3-I
- iodotrifluoromethane
-
SMILESC(F)(F)(F)I
-
InChIKeyVPAYJEUHKVESSD-UHFFFAOYSA-N
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Similar Compounds
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