| Weight | 176.093 g/mol |
|---|---|
| Formula | C7H3F3O2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,4,5-Trifluorobenzoic acid (446-17-3)
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- The continuous flow synthesis of 2,4,5-trifluorobenzoic acid via sequential Grignard exchange and carboxylation reactions using microreactors (Chemical Engineering Journal, 2015)
- Synthesis of mono- and di-substituted 2,4,5-trifluorobenzoic acid synthons, key precursors for biologically active 6-fluoroquinolones (Tetrahedron, 2005)
- An Expedient Route to the Quinolone Antibacterial Intermediate, 2,4,5-Trifluorobenzoic Acid (Synlett, 1990)
- Process Improvements in the Synthesis of 2,4,5-Trifluorobenzoic Acid. Selective Hydrodefluorination of Tetrafluorophthalimides (Organic Process Research & Development, 1998)
- The synthesis of 3-bromo-2,4,5-trifluorobenzoic acid and its conversion to 8-bromoquinolonecarboxylic acids (Journal of Heterocyclic Chemistry, 1996)
- Method of making 3-hydroxy-2,4,5-trifluorobenzoic acid (1982)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C(=CC(=C1F)F)F)C(=O)O
-
InChIKeyAKAMNXFLKYKFOJ-UHFFFAOYSA-N
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