| Weight | 113.038 g/mol |
|---|---|
| Formula | C2H2F3NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Trifluoroacetamide (354-38-1)
Score:
#2581 in Biochemistry
,
#6419 in Chemistry
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- Optimization of silylation using N-methyl-N-(trimethylsilyl)-trifluoroacetamide, N,O-bis-(trimethylsilyl)-trifluoroacetamide and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide for the determination of the estrogens estrone and 17-ethinylestradiol by gas chromatographymass spectrometry (Journal of Chromatography A, 2006)
- A new silylation reagent for amino acids bis (trimethylsilyl)trifluoroacetamide (BSTFA) (Biochemical and Biophysical Research Communications, 1968)
- N-Methyl-N-(tert-butyldimethylsilyl)trifluoroacetamide and related N-tert-butyldimethylsilyl amides as protective silyl donors (Journal of Organic Chemistry, 1982)
- Pitfalls and solution for simultaneous determination of estrone and 17-ethinylestradiol by gas chromatography-mass spectrometry after derivatization with N,O-bis (trimethylsilyl )trifluoroacetamide (Analytica Chimica Acta, 2005)
- Suitability of N, O-bis(trimethylsilyl)trifluoroacetamide and N-(tert-butyldimethylsilyl)-N-methyltrifluoroacetamide as derivatization reagents for the determination of the estrogens estrone and 17-ethinylestradiol by gas chromatography-mass spectrometry (Journal of Chromatography A, 2004)
- Copper-catalyzed synthesis of primary arylamines from aryl halides and 2,2,2-trifluoroacetamide (Tetrahedron Letters, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=O)(C(F)(F)F)N
-
InChIKeyNRKYWOKHZRQRJR-UHFFFAOYSA-N
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Similar Compounds
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Trifluoroacetamide
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