Weight | 216.158 g/mol |
---|---|
Formula | C10H7F3O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
326-06-7 (326-06-7)
4,4,4-TFBP · 4,4,4-trifluoro-1-phenyl-1,3-butanedione
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- Synthesis, luminescence and quantum yields of Eu(III) mixed complexes with 4,4,4-trifluoro-1-phenyl-1,3-butanedione and 1,10-phenanthroline-N-oxide (Journal of Alloys and Compounds, 1997)
- Syntheses, crystal structures, visible and near-IR luminescent properties of ternary lanthanide (Dy3+, Tm3+) complexes containing 4,4,4-trifluoro-1-phenyl-1,3-butanedione and 1,10-phenanthroline (Journal of Luminescence, 2008)
- ENHANCED EXTRACTION AND SEPARATION OF TRIVALENT LANTHANOIDS WITH 4,4,4-TRIFLUORO-1-PHENYL-1,3-BUTANEDIONE AND CROWN ETHER (Radiochimica Acta, 1998)
- Mixed-ligand chelate extraction of trivalent lanthanides with 4,4,4-trifluoro-1-phenyl-1,3-butanedione and neutral oxo-donors (Talanta, 1997)
- Thermal decomposition of lanthanide(III) complexes with 4,4,4 -trifluoro -1 -phenyl -1,3 -butanedione : Photoluminescent properties and kinetic study (Journal of Thermal Analysis and Calorimetry, 2007)
- The temperature dependence of the solubilities of 1-phenyl-1,3-butanedione and 4,4,4-trifluoro-1-phenyl-1,3-butanedione in water and aqueous electrolyte solutions. (Bulletin of the Chemical Society of Japan, 1978)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4,4,4-TFBP
- 4,4,4-trifluoro-1-phenyl-1,3-butanedione
-
SMILESC1=CC=C(C=C1)C(=O)CC(=O)C(F)(F)F
-
InChIKeyVVXLFFIFNVKFBD-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
benzene
+
Reactant
(Friedel-Crafts acylation)
Reactant
+
CHLOROBENZENE
(Grignard carbonyl)
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