| Weight | 190.12 g/mol |
|---|---|
| Formula | C8H5F3O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Phenyl trifluoroacetate (500-73-2)
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- Synthesis of Trifluoromethyl Ketones by Palladium-Catalyzed Cross-Coupling Reaction of Phenyl Trifluoroacetate with Organoboron Compounds (Bulletin of the Chemical Society of Japan, 2001)
- A Novel and Direct Alkyl Azidation of p-Alkylanisoles Using Phenyl Iodine(III) Bis(trifluoroacetate) (PIFA) and Trimethylsilyl Azide (Synlett, 1994)
- Pummerer-type reaction of -acylsulfides using phenyl iodosyl bis(trifluoroacetate) (Chemical & Pharmaceutical Bulletin, 1986)
- Phenyliodine Bis(trifluoroacetate) Mediated Intramolecular Oxidative Coupling of Electron-Rich N-Phenyl Benzamides (Synlett, 2012)
- A Novel and Direct Sulfenylation of Phenol Ethers Using Phenyl Iodine(III) Bis(trifluoroacetate) (PIFA) and Various Thiophenols (Synlett, 1995)
- A new carbon-carbon bond forming reaction in indole chemistry. C3-Arylation and alkylation with phenyl (-indolyl) iodonium trifluoroacetate (Tetrahedron Letters, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)OC(=O)C(F)(F)F
-
InChIKeyDVCMYAIUSOSIQP-UHFFFAOYSA-N
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Phenyl trifluoroacetate
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