425664

Dysprosium(III) trifluoromethanesulfonate

98%

• Sinónimos: Dysprosium(III) triflate, Tris(triflato)dysprosium
• Fórmula lineal: (CF₃SO₃)₃Dy
• Número de CAS: 139177-62-1
• Peso molecular: 609.71
• MDL number: MFCD00209583
• UNSPSC Code: 12161600
• PubChem Substance ID: 24866655
• NACRES: NA.22

Propiedades

• assay: 98%
• 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
• 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

Descripción

General description

Dysprosium(III) trifluoromethanesulfonate (Dysprosium(III) triflate) is a lanthanide triflate.

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

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).

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H315,H319,H335
• pcodes: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves