| Stereochemistry | ACHIRAL |
| Molecular Formula | 3C5H7O2.Fe |
| Molecular Weight | 353.169 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Fe+3].CC(=O)[CH-]C(C)=O.CC(=O)[CH-]C(C)=O.CC(=O)[CH-]C(C)=O
InChI
InChIKey=KAMWVXQBCBPBND-UHFFFAOYSA-N
InChI=1S/3C5H7O2.Fe/c3*1-4(6)3-5(2)7;/h3*3H,1-2H3;/q3*-1;+3
| Molecular Formula | Fe |
| Molecular Weight | 55.845 |
| Charge | 3 |
| Count |
MOL RATIO
1 MOL RATIO (average) |
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C5H8O2 |
| Molecular Weight | 100.1158 |
| Charge | 0 |
| Count |
MOL RATIO
3 MOL RATIO (average) |
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Ferric acetylacetonate, often abbreviated Fe(acac)3, is a ferric coordination complex featuring acetylacetonate (acac) ligands. Fe(acac)3 has been examined as a precatalyst and reagent in organic chemistry. Can be used as a catalyst in preparation, degradation, and calcification of biodegradable polyurethane foams for bone graft substitutes. Thermal decomposition of Fe(acac)(3) in triethylene glycol has being used in the synthesis of water-stable magnetite nanoparticles for clinical MRI and magnetic hyperthermia applications.
Approval Year
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
PubMed
Patents
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PARENT -> SALT/SOLVATE | |||
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PARENT -> SALT/SOLVATE |
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