| Weight | 112.05 g/mol |
|---|---|
| Formula | C3H3F3O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,1,1-Trifluoro-2,3-epoxypropane (359-41-1)
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LabBot
- The Ring-cleavage Reactions of 1,1,1-Trifluoro-2,3-epoxypropane (Journal of the American Chemical Society, 1956)
- The Ethanolysis of 1,1,1-Trifluoro-2,3-epoxybutane and 2-Methyl-1,1,1-trifluoro-2,3-epoxypropane (Journal of the American Chemical Society, 1956)
- Highly Stereocontrolled Access to 1,1,1-Trifluoro-2,3-epoxypropane via Lipase-Mediated Kinetic Resolution of 1,1,1-Trifluoro-3-(phenylthio)propan-2-ol and Its Application (Bulletin of the Chemical Society of Japan, 1996)
- Copolymerization of 3,3,3-trifluoro-1,2-epoxypropane with N-phenylmaleimide using organozinc initiators (Macromolecular Rapid Communications, 1996)
- Copolymerization of 3,3,3-trifluoro-1,2-epoxypropane with 1,2-epoxypropane using organozinc compounds (Macromolecules, 1995)
- Structural study of polymeric 3,3,3-trifluoro-1,2-epoxypropane (Polymer Science U.s.s.r., 1970)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(O1)C(F)(F)F
-
InChIKeyAQZRARFZZMGLHL-UHFFFAOYSA-N
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