Weight | 114.066 g/mol |
---|---|
Formula | C3H5F3O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
1,1,1-Trifluoropropan-2-ol (374-01-6)
1,1,1-trifluoro-2-propanol
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- (N-Isocyanimino)triphenylphosphorane-Mediated, One-Pot, Efficient Synthesis of Sterically Congested 1,1,1-Trifluoro-2-(5-aryl-1,3,4-oxadiazol-2-yl)-2-propanol Derivatives via Intramolecular Aza-Wittig Reaction (Phosphorus Sulfur and Silicon and The Related Elements, 2010)
- FluoroalcoholsXXI. Infrared, matrix infrared and Raman spectra of 1,1,1-trifluoro-2-propanol and its three deuterated analogues (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1975)
- Synthesis of 3-trifluoromethylpyrazoles and 3-trifluoromethylpyridazines from 2-amino-1,1,1-trifluoro-3-phenylsulfonyl-2-propanol (Heterocycles, 1993)
- Tin oxide surfaces. Part 21.Infrared study of the chemisorption of 2,2,2-trifluoroethanol, 1,1,1,3,3,3-hexafluoropropan-2-ol, 1,1,1-trifluoropropan-2-one, 1,1,1,3,3,3-hexafluoropropan-2-one and trifluoroacetic acid on tin(IV) oxide gel (Journal of the Chemical Society, Faraday Transactions, 1991)
- Far-infrared and Raman spectra of gaseous 1,1,1-trifluoro-2-propanol: conformational stability and barriers to internal rotation (The Journal of Physical Chemistry, 1987)
- The influence of trifluoromethyl groups on the miscibility of fluorinated alcohols with water: A molecular dynamics simulation study of 1,1,1-trifluoropropan-2-ol in aqueous solution (Journal of Physical Chemistry B, 2003)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,1,1-trifluoro-2-propanol
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SMILESCC(C(F)(F)F)O
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InChIKeyGILIYJDBJZWGBG-UHFFFAOYSA-N
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