| Weight | 209.936 g/mol |
|---|---|
| Formula | C2H2F3I |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,1,1-Trifluoro-2-iodoethane (353-83-3)
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- Palladium-catalyzed trifluoroethylation of terminal alkynes with 1,1,1-trifluoro-2-iodoethane. (Organic Letters, 2013)
- A simple preparation of iodoarenes, iodoalkenes and iodoalkynes by reaction of organolithiums with 2,2,2-trifluoro-1-iodoethane (Tetrahedron Letters, 1999)
- Copper-promoted reductive coupling of aryl iodides with 1,1,1-trifluoro-2-iodoethane. (Organic Letters, 2014)
- Visible-Light-Induced Photocatalysis of 1,1,1-Trifluoro-2-iodoethane with Alkylalkenes and Silyl Enol Ethers (Synthesis, 2015)
- Femtosecond photodissociation dynamics of 1,1,1-trifluoro-2-iodoethane in the Franck-Condon region (Molecular Physics, 1997)
- Vibrational studies and ab initio calculations of the conformers of 1,2-dichloro-1,1,2-trifluoro-2-iodoethane (Journal of Fluorine Chemistry, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C(F)(F)F)I
-
InChIKeyRKOUFQLNMRAACI-UHFFFAOYSA-N
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Similar Compounds
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1,1,1-Trifluoro-2-iodoethane
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