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Scandium(III) trifluoromethanesulfonate

Base Information Edit
  • Chemical Name:Scandium(III) trifluoromethanesulfonate
  • CAS No.:144026-79-9
  • Molecular Formula:C3F9O9S3Sc
  • Molecular Weight:492.16
  • Hs Code.:28469099
  • European Community (EC) Number:629-306-8
  • DSSTox Substance ID:DTXSID70370368
  • Nikkaji Number:J742.234B
  • Wikipedia:Scandium(III)_trifluoromethanesulfonate,Scandium(III) triflate
  • Wikidata:Q6364879
  • Mol file:144026-79-9.mol
Scandium(III) trifluoromethanesulfonate

Synonyms:Sc(OTf)3;scandium triflate;scandium(III) trifluoromethanesulfonate

Suppliers and Price of Scandium(III) trifluoromethanesulfonate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • ScandiumTriflate
  • 25g
  • $ 425.00
  • TCI Chemical
  • Scandium(III) Trifluoromethanesulfonate >98.0%(T)
  • 1g
  • $ 50.00
  • TCI Chemical
  • Scandium(III) Trifluoromethanesulfonate >98.0%(T)
  • 5g
  • $ 169.00
  • SynQuest Laboratories
  • Scandium(III) trifluoromethanesulfonate 99%
  • 25 g
  • $ 450.00
  • SynQuest Laboratories
  • Scandium(III) trifluoromethanesulfonate 99%
  • 5 g
  • $ 125.00
  • SynQuest Laboratories
  • Scandium(III) trifluoromethanesulfonate 99%
  • 1 g
  • $ 45.00
  • Strem Chemicals
  • Scandium(III) trifluoromethanesulfonate, min. 98% (Scandium triflate)
  • 250mg
  • $ 24.00
  • Strem Chemicals
  • Scandium(III) trifluoromethanesulfonate, min. 98% (Scandium triflate)
  • 1g
  • $ 54.00
  • Strem Chemicals
  • Scandium(III) trifluoromethanesulfonate, min. 98% (Scandium triflate)
  • 5g
  • $ 187.00
  • Sigma-Aldrich
  • Scandium(III) triflate 97%
  • 5g
  • $ 167.00
Total 91 raw suppliers
Chemical Property of Scandium(III) trifluoromethanesulfonate Edit
Chemical Property:
  • Appearance/Colour:white powder 
  • Melting Point:>300 °C 
  • Boiling Point:162ºC at 760 mmHg 
  • PSA:196.74000 
  • LogP:3.39660 
  • Storage Temp.:Inert atmosphere,Room Temperature 
  • Sensitive.:Hygroscopic 
  • Solubility.:Water (Slightly) 
  • Water Solubility.:Soluble in water, alcohol and acetonitrile. 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:18
  • Rotatable Bond Count:0
  • Exact Mass:491.811981
  • Heavy Atom Count:25
  • Complexity:145
Purity/Quality:

98.0% *data from raw suppliers

ScandiumTriflate *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[Sc+3]
  • Description Scandium trifluoromethanesulfonate, commonly called Scandium(III) triflate, is a chemical compound with formula Sc(SO3CF3)3, a salt consisting of scandium cations Sc3+ and triflate SO3CF3? anions.Scandium(III) triflate 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) triflate complex of (4′S,5′S)-2,6-bis[4′-(triisopropylsilyl)oxymethyl-5′-phenyl-1′,3′-oxazolin-2′-yl]pyridine has been employed as catalyst for the asymmetric Friedel-Crafts reaction between substituted indoles and methyl (E)-2-oxo-4-aryl-3-butenoates.
  • Uses 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. Scandium Triflate is an important catalyst used in Friedel-Crafts acylation, Baylis-Hillman reaction and other carbon-carbon bond forming reactions.
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