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Dysprosium(III) trifluoromethanesulfonate

ALDRICH/425664 - 98%

Synonym: Dysprosium(III) triflate; Tris(triflato)dysprosium

CAS Number: 139177-62-1
Empirical Formula (Hill Notation): C3DyF9O9S3
Molecular Weight: 609.71
MDL Number: MFCD00209583
Linear Formula: (CF3SO3)3Dy
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-425664-5G 5 g
$201.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 425664-5G

 

assay 98%
InChI 1S/3CHF3O3S.Dy/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3
InChI key XSVCYDUEICANRJ-UHFFFAOYSA-K
reaction suitability core: dysprosium
  reagent type: catalyst
reaction type: Ring-Opening Polymerization
SMILES string [Dy+3].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F
Application: Catalyst for:
• Aza-Piancatelli rearrangement
• Friedel-Crafts alkylation
• Ring-opening polymerization reactions
• Microwave-assisted Kabachnik-Fields condensation
• Cycloaddition reactions (Lewis-acid catalyst)
• Fries rearrangement
• Enantioselective glyoxalate-ene reactions
Application: Dysprosium(III) trifluoromethanesulfonate, a water-tolerant Lewis acid, has been used in the following studies:
• Aldol reaction of silyl enol ethers with aldehydes.
• As an effective catalyst for electrophilic substitution reactions of indoles with imines.
• As catalyst for the synthesis of 4-aminocyclopentenones and functionalized azaspirocycles, via intramolecular aza-Piancatelli rearrangement.
• As new curing initiator to study the curing of diglycidyl ether of bisphenol-A (DGEBA).
General description: Dysprosium(III) trifluoromethanesulfonate (Dysprosium(III) triflate) is a lanthanide triflate.
Packaging: 5, 25 g in glass bottle
Purity 98%
UNSPSC 12161600

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