Weight | 130.065 g/mol |
---|---|
Formula | C3H5F3O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
Trifluoroacetaldehyde methyl hemiacetal (431-46-9)
2,2,2-trifluoro-1-methoxyethanol
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- Organocatalytic Asymmetric Direct Aldol Reactions of Trifluoroacetaldehyde Ethyl Hemiacetal with Aromatic Methyl Ketones (Journal of Organic Chemistry, 2011)
- One-pot preparation of trifluoromethylated homoallylic N-acylhydrazines or -methylene--lactams from acylhydrazines, trifluoroacetaldehyde methyl hemiacetal, allyl bromide and tin. (Organic and Biomolecular Chemistry, 2016)
- ChemInform Abstract: Reversal of Diastereoselectivity in Reactions of the Trifluoroacetaldehyde Ethyl Hemiacetal with Enamines and Imines: Metal-Free, Complementary anti- and syn-Selective Synthesis of 4,4,4-Trifluoro-1-aryl-3-hydroxy-2-methyl-1-butanones. (ChemInform, 2011)
- 2,2,2Trifluoro1methoxyethanol (2013)
- ChemInform Abstract: Organocatalytic Asymmetric Direct Aldol Reactions of Trifluoroacetaldehyde Ethyl Hemiacetal with Aromatic Methyl Ketones. (ChemInform, 2011)
- Environmentally benign, microwave-assisted regioselective N-hydroxyalkylation of indoles with trifluoroacetaldehyde methyl hemiacetal (Arkivoc, 2017)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,2,2-trifluoro-1-methoxyethanol
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SMILESCOC(C(F)(F)F)O
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InChIKeyGWTBCUWZAVMAQV-UHFFFAOYSA-N
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