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Ytterbium(III) Trifluoromethanesulfonate Hydrate CAS 54761-04-5 Purity >98.0% (Chelometric Titration)

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Ytterbium(III) Trifluoromethanesulfonate Hydrate (CAS: 54761-04-5) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com
Chemical Name Ytterbium(III) Trifluoromethanesulfonate Hydrate
Synonyms Trifluoromethanesulfonic Acid Ytterbium(III) Salt Hydrate; Ytterbium(III) Triflate Hydrate
CAS Number 54761-04-5
CAT Number RF-PI2097
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C3F9O9S3Yb·xH2O
Molecular Weight 620.24
Sensitive Hygroscopic
Brand Ruifu Chemical
Item Specifications
Appearance Off-White or Light Gray Powder
Purity / Analysis Method >98.0% (Chelometric Titration) (Calcd. on Anhydrous Substance)
Water (by Karl Fischer) ≤4.00%
Infrared Spectrum Conforms to Structure
X-Ray Diffraction Conforms to Structure
Test Standard Enterprise Standard
Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture Ytterbium(III) Trifluoromethanesulfonate Hydrate (CAS: 54761-04-5) functions as a catalyst in the organic synthesis of heterocycles. Also functions as a Lewis acid in variety of organic reactions. Versatile rare earth metal catalyst in organic synthesis. A water-tolerant Lewis acid catalyst recently used in one-pot syntheses of β-lactams, and in stereocontrolled radical and nucleophilic addition reactions. Catalyzes the synthesis of deoxypenostatin A in a novel, stereoselective, intramolecular Diels-Alder reaction. Lewis acid catalyst used with a silylated chinchona alkaloid in an asymmetric synthesis of substituted β-lactams from an acid chloride and aryl imine. Also used to catalyze an aldehyde-ene reaction in a synthesis of the guaiane skeleton. An important Lewis acid catalyst for a variety of synthetic reactions, including allylborations.