Tris(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedionato)ytterbium

Base Information

• Chemical Name: Tris(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedionato)ytterbium
• CAS No.: 18323-96-1
• Molecular Formula: C30H30F21O6Yb
• Molecular Weight: 1058.56
• Hs Code.: 28469000
• European Community (EC) Number: 242-211-2
• Mol file: 18323-96-1.mol

Synonyms:18323-96-1;C30H30F21O6Yb;Yb[fod]3;Tris(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedionato)ytterbium;C30-H30-F21-O6-Yb;YTTERBIUM-FOD;Ytterbium, tris(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedionato-.beta.O3,.beta.O5)-

Chemical Property of Tris(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedionato)ytterbium

Chemical Property:

• Appearance/Colour: off-white to yellow crystalline powder
• Vapor Pressure: 0.0812mmHg at 25°C
• Melting Point: 108-111 °C(lit.)
• Boiling Point: 200.3 °C at 760 mmHg
• Flash Point: 74.9 °C
• PSA: 78.90000
• LogP: 11.39790
• Sensitive.: Hygroscopic
• Water Solubility.: Slowly degrades in water and soluble in hydrocarbons, alcohols, ketones, esters.
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 27
• Rotatable Bond Count: 12
• Exact Mass: 1059.1095726
• Heavy Atom Count: 58
• Complexity: 388

Purity/Quality:

98%,99%, ^*data from raw suppliers

Tris(6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedionate)ytterbium(III), 99% (99.9%-Yb) (REO) [Yb(FOD)3] ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC(C)(C)C(=CC(=O)C(C(C(F)(F)F)(F)F)(F)F)[O-].CC(C)(C)C(=CC(=O)C(C(C(F)(F)F)(F)F)(F)F)[O-].CC(C)(C)C(=CC(=O)C(C(C(F)(F)F)(F)F)(F)F)[O-].[Yb+3]
• Isomeric SMILES: CC(/C(=C/C(=O)C(F)(F)C(F)(F)C(F)(F)F)/[O-])(C)C.CC(/C(=C/C(=O)C(F)(F)C(F)(F)C(F)(F)F)/[O-])(C)C.CC(/C(=C/C(=O)C(F)(F)C(F)(F)C(F)(F)F)/[O-])(C)C.[Yb+3]
• Uses: It is a reactant involved in the synthesis of rare earth metal complexes for separation of lanthanide metals, conformational mobility of substituted 2-methoxychalcones under the action of lanthanide shift reagents, NMR titration on cation-π complexes of bowl-shaped polycyclic aromatic hydrocarbons, specific recognition of chiral amino alcohols. It finds its application as catalysis and synthesis, optics & glasses, healthcare & biochemical.