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144026-79-9

144026-79-9 Structure

144026-79-9 Structure
IdentificationMore
[Name]

Scandium trifluoromethanesulfonate
[CAS]

144026-79-9
[Synonyms]

PS-SC(OTF)2
SCANDIUM(III) TRIFLATE
SCANDIUM(III) TRIFLUOROMETHANESULFONATE
SCANDIUM(III) TRIFLUOROMETHANESULPHONATE
SCANDIUM TRIFLATE
SCANDIUM TRIFLATE RESIN
SCANDIUM TRIFLUOROMETHANESULFONATE
SCANDIUM TRIFLUOROMETHANESULFONATE, POLYMER-BOUND
SC(O3SCF3)3
TRIFLUOROMETHANESULFONIC ACID SCANDIUM(3) SALT
TRIFLUOROMETHANESULFONIC ACID SCANDIUM(III) SALT
TRIFLUOROMETHANESULFONIC ACID SCANDIUM SALT
Scandium (lll) trifluoromethanesulfonate
Scandium(III) triflate, 99.995% metals basis
SCANDIUM (III) TRIFLUOROMETHANESULFONATE, 97+% (SCANDIUM TRIFLATE)
ScandiumTrifluoromethanesulfonate,Microencapsulated
Scandium(III)trifluoromethanesulfonate,min.97%(Scandiumtriflate)
Methanesulfonic acid, trifluoro-, scandium(3+) salt
Scandium(III) trifluoromethanesulphonate 99%
Scandium(III)trifluoromethanesulphonate99%
[Molecular Formula]

C3F9O9S3Sc
[MDL Number]

MFCD00192433
[Molecular Weight]

492.16
[MOL File]

144026-79-9.mol
Chemical PropertiesBack Directory
[Appearance]

White powder
[Melting point ]

>300 °C
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Water (Slightly)
[form ]

Powder
[color ]

White
[Water Solubility ]

Soluble in water, alcohol and acetonitrile.
[Hydrolytic Sensitivity]

6: forms irreversible hydrate
[Sensitive ]

Hygroscopic
[BRN ]

8510151
[Stability:]

hygroscopic
[InChI]

InChI=1S/3CHF3O3S.Sc/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3
[InChIKey]

HZXJVDYQRYYYOR-UHFFFAOYSA-K
[SMILES]

C(F)(S([O-])(=O)=O)(F)F.C(F)(F)(F)S([O-])(=O)=O.C(F)(F)(F)S([O-])(=O)=O.[Sc+3]
[CAS DataBase Reference]

144026-79-9(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[F ]

3-10
[Hazard Note ]

Irritant
[TSCA ]

No
[HS Code ]

28469099
Hazard InformationBack Directory
[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.
[Chemical Properties]

White powder
[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.?
[Application]

Scandium(III) triflate was used as a catalyst in:
Hydrothiolation reaction of aromatic and aliphatic thiols.
Selective two-electron reduction of O2 by ferrocene derivatives.
Vinylogous Friedel-Crafts alkylation of indoles and pyrroles in water.
Synthesis of β-cyanoketones.
Combination with triethylsilane to reductively open functionalized pyranoside rings.
The key steps of synthesis of bullvalone via a stabilized sulfur ylide.
[Reactions]

  1. Water tolerant Lewis acid.
  2. Commonly used in a range of Lewis acid catalyzed reactions.
  3. Efficient metal source for Lewis acid catalyzed asymmetric reactions.
  4. Catalyzes Friedel-Crafts alkylation, acylation and related reactions.
  5. Catalyzes various domino- and multi-component processes.
  6. Catalyzes electrophilic additions of alpha-diazoesters with ketones.
  7. Catalyzes carbon insertion reactions.


[General Description]

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.
Spectrum DetailBack Directory
[Spectrum Detail]

Scandium trifluoromethanesulfonate(144026-79-9)FT-IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Scandium(III) trifluoromethanesulfonate, 95%(144026-79-9)
[Alfa Aesar]

Scandium(III) trifluoromethanesulfonate, 98%(144026-79-9)
[Sigma Aldrich]

144026-79-9(sigmaaldrich)
[TCI AMERICA]

Scandium(III) Trifluoromethanesulfonate,>98.0%(T)(144026-79-9)
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