| Weight | 222.187 g/mol |
|---|---|
| Formula | C8H5F3O2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
2-Thenoyltrifluoroacetone (326-91-0)
Thenoyltrifluoroacetone · TTFA cpd · 4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedione
Score:
#1628 in Physics
,
#1824 in Biochemistry
,
#4990 in Chemistry
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- Enhanced luminescence of the europium/terbium/thenoyltrifluoroacetone/1,10-phenanthroline/surfactant system, and its analytical application (Analytica Chimica Acta, 1987)
- Solvent extraction of metal ions with mixed ligandsI: Adduct formation of Cu(II) and Zn(II) chelate complexes of thenoyltrifluoroacetone and -isopropyltropolone (Journal of Inorganic and Nuclear Chemistry, 1964)
- Spectrophotometric determination of zirconium, uranium, thorium and rare earths with arsenazo III after extractions with thenoyltrifluoroacetone and tri-n-octylamine (Talanta, 1972)
- Comparative study of the luminescent properties of europium and terbium coordinated with thenoyltrifluoroacetone or pyridine-2,6-dicarboxylic acid in aqueous solutions (Analyst, 1998)
- Hybrid materials of lanthanide centers/functionalized 2-thenoyltrifluoroacetone/silicon-oxygen network/polymeric chain: coordination bonded assembly, physical characterization, and photoluminescence. (Inorganic Chemistry, 2009)
- EXTRACTION OF URANYL ION FROM SOME AQUEOUS SALT SOLUTIONS WITH 2- THENOYLTRIFLUOROACETONE (Journal of the American Chemical Society, 1954)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Thenoyltrifluoroacetone
- TTFA cpd
- 4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedione
- Trifluorothienylacetone
-
SMILESC1=CSC(=C1)C(=O)CC(=O)C(F)(F)F
-
InChIKeyTXBBUSUXYMIVOS-UHFFFAOYSA-N
- Pubchem - 2-Thenoyltrifluoroacetone
- Wikipedia - thenoyltrifluoroacetone
Thenoyltrifluoroacetone, C8H5F3O2S, is a chemical compound used pharmacologically as a chelating agent. It is an inhibitor of cellular respiration by blocking the respiratory chain at complex II. Perhaps the first report of TTFA as an inhibitor of respiration was by A.
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Synthesis
THIOPHENE
+
Reactant
(Friedel-Crafts acylation)
Reactant
+
2-CHLOROTHIOPHENE
(Grignard carbonyl)
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