Scandium(III) Trifluoromethanesulfonate CAS 144026-79-9 Purity >98.0% (Chelometric Titration) Scandium >9.0%

Short Description:

Name: Scandium(III) Trifluoromethanesulfonate

Synonyms: Scandium(III) Triflate

CAS: 144026-79-9

Purity: >98.0% (Chelometric Titration)

Scandium: >9.0% (Complexometric EDTA)

Appearance: White Powder

E-Mail: alvin@ruifuchem.com

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Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Scandium(III) Trifluoromethanesulfonate (CAS: 144026-79-9) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Chemical Properties:

Chemical Name	Scandium(III) Trifluoromethanesulfonate
Synonyms	Scandium(III) Triflate; Scandium Trifluoromethanesulfonate; Trifluoromethanesulfonic Acid Scandium(III) Salt; Sc(OTf)3 ; Sc(SO3CF3)3
CAS Number	144026-79-9
CAT Number	RF-PI2108
Stock Status	In Stock, Production Scale Up to Tons
Molecular Formula	Sc(SO3CF3)3
Molecular Weight	492.16
Sensitivity	Hygroscopic
Melting Point	>300℃
Solubility	Soluble in Water, Alcohol and Acetonitrile
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Appearance	White Powder
Purity / Analysis Method	>98.0% (Chelometric Titration)
Scandium	>9.0% (Complexometric EDTA)
Infrared Spectrum	Conforms to Structure
X-Ray Diffraction	Conforms to Structure
Test Standard	Enterprise Standard

Package & Storage:

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

Advantages:

FAQ:

Application:

Scandium(III) Trifluoromethanesulfonate, also known as Scandium(III) Triflate, (CAS: 144026-79-9) is an extremely active, efficient, recoverable and reusable acylation catalyst. Its an important catalyst for the Friedel-Crafts acylation, Diels-Alder reactions and other carbon-carbon bond-forming reactions. It also stereochemically catalyzes the radical polymerization of acrylates. Scandium(III) Trifluoromethanesulfonate is widely used as a catalyst in hydrothiolation, selective two-electron reduction of oxygen by ferrocene derivatives and vinylogous Fridel-crafts alkylation of indoles and pyrrole in water. It is involved in the Mukaiyama aldol addition and stereochemically catalyzes the radical polymerization of acrylates. It acts as a Lewis acid catalyst and used in the synthesis of bullvalone via a stabilized sulfur ylide. Reactions: Water tolerant Lewis acid. Commonly used in a range of Lewis acid catalyzed reactions. Efficient metal source for Lewis acid catalyzed asymmetric reactions. Catalyzes Friedel-Crafts alkylation, acylation and related reactions. Catalyzes various domino- and multi-component processes. Catalyzes electrophilic additions of alpha-diazoesters with ketones. Catalyzes carbon insertion reactions.