| Weight | 189.136 g/mol |
|---|---|
| Formula | C8H6F3NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,2,2-Trifluoro-N-phenylacetamide (404-24-0)
trifluoroacetanilide · trifluoro-acetanilide
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- 6-Aryl-11H-indolo[3,2-c]quinolines through the Palladium-Catalyzed Carbonylative Cyclization of o-(o-Aminophenyl)trifluoroacetanilide with Aryl Iodides (Synlett, 1999)
- Trifluoroacetanilide. pKaand Alkaline Hydrolysis Kinetics (Journal of the American Chemical Society, 1965)
- Hydrolysis of Anilides. IV. Hydroxylaminolysis, Hydrazinolysis, and General Acid-Catalysed Alkaline Hydrolysis of Trifluoroacetanilide. (Acta Chemica Scandinavica, 1968)
- Water Catalyzed Hydrolysis of p-Nitrotrifluoroacetanilide and Trifluoroacetanilide. Carbonyl 18O-Exchange Does Not Accompany the Water Reaction (Journal of the American Chemical Society, 1997)
- Hydrolysis of Anilides. III. Aminolysis and General Acid-Catalysed Alkaline Hydrolysis of Trifluoroacetanilide. (Acta Chemica Scandinavica, 1967)
- Amine catalysis of the hydrolysis of trifluoroacetanilide (Journal of Organic Chemistry, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - trifluoroacetanilide
- trifluoro-acetanilide
-
SMILESC1=CC=C(C=C1)NC(=O)C(F)(F)F
-
InChIKeySAPQIENQEZURNZ-UHFFFAOYSA-N
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