Home Categories Organic Chemistry Scandium(III) triflate
A7287612

Scandium(III) triflate , 98% , 144026-79-9

Synonym(s):
Sc(OTf)3;Sc(OTf)3;Scandium tris(trifluoromethanesulfonate);Scandium(III) trifluoromethanesulfonate;Trifluoromethanesulfonic acid scandium(III) salt

CAS NO.:144026-79-9

Empirical Formula: C3F9O9S3Sc

Molecular Weight: 492.16

MDL number: MFCD00192433

Pack Size Price Stock Quantity
250MG RMB25.60 In Stock
1G RMB45.60 In Stock
5G RMB148.80 In Stock
10g RMB311.20 In Stock
25G RMB515.20 In Stock
100g RMB1808.80 In Stock
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Update time: 2022-07-08

PRODUCT Properties

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.
Sensitive  Hygroscopic
Hydrolytic Sensitivity 6: forms irreversible hydrate
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]

Description and Uses

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.

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.

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338-P280a-P304+P340-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
3-10
Hazard Note  Irritant
TSCA  No
HS Code  28469099

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