Weight | 208.057 g/mol |
---|---|
Formula | C5H2F6O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
Hexafluoroacetylacetone (1522-22-1)
Score:
#372 in Materials science
,
#2338 in Physics
,
#7178 in Chemistry
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- Nature of Copper(II)Lanthanide(III) Magnetic Interactions and Generation of a Large Magnetic Moment with Magnetic Anisotropy of 3d4f Cyclic Cylindrical Tetranuclear Complexes [CuIILLnIII(hfac)2]2, (H3L = 1-(2-Hydroxybenzamido)-2-(2-hydroxy-3-methoxybenzylideneamino)ethane and Hhfac = Hexafluoroacetylacetone, LnIII = Eu, Gd, Tb, Dy) (Inorganic Chemistry, 2003)
- NormalCoordinate Analyses of HydrogenBonded Compounds. V. The Enol Forms of Acetylacetone and Hexafluoroacetylacetone (Journal of Chemical Physics, 1966)
- Hexafluoroacetylacetone and hexafluoroacetic anhydride (Journal of the American Chemical Society, 1971)
- Gas Phase Chromatography of Metal Chelates of Acetylacetone, Trifluoroacetylacetone, and Hexafluoroacetylacetone (Inorganic Chemistry, 1963)
- INFRARED SPECTRA OF METAL CHELATE COMPOUNDS OF HEXAFLUOROACETYLACETONE (Inorganic Chemistry, 1963)
- Syntheses, Structures, and Properties of Trinuclear Complexes [M(bpca)2{M(hfac)2}2], Constructed with the Complexed Bridging Ligand [M(bpca)2] [M, M = Ni(II), Mn(II); Cu(II), Mn(II); Fe(II), Mn(II); Ni(II), Fe(II); and Fe(II), Fe(II); Hbpca = Bis(2-pyridylcarbonyl)amine, Hhfac = Hexafluoroacetylacetone] (Inorganic Chemistry, 2002)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C(=O)C(F)(F)F)C(=O)C(F)(F)F
-
InChIKeyQAMFBRUWYYMMGJ-UHFFFAOYSA-N
- Pubchem - Hexafluoroacetylacetone
- Wikipedia - Hexafluoroacetylacetone
Hexafluoroacetylacetone is the chemical compound with the nominal formula CF3C(O)CH2C(O)CF3 (often abbreviated as hfacH). This colourless liquid is a ligand precursor and a reagent used in MOCVD. The compound exists exclusively as the enol CF3C(OH)=CHC(O)CF3.
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Synthesis
Reactant
+
Trifluoromethyl chloride
(Grignard carbonyl)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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