Copper(II) Trifluoromethanesulfonate CAS 34946-82-2 Purity >98.0% (Titration) Factory

Short Description:

Name: Copper(II) Trifluoromethanesulfonate

Synonyms: Copper(II) Triflate; Cu(OTf)2

CAS: 34946-82-2

Purity: >98.0% (Titration) 

Appearance: Off-White to Light Blue Solid

E-Mail: alvin@ruifuchem.com


Product Detail

Related Products

Product Tags

Description:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Copper(II) Trifluoromethanesulfonate (CAS: 34946-82-2) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Chemical Properties:

Chemical Name Copper(II) Trifluoromethanesulfonate
Synonyms Copper Trifluoromethanesulfonate; Copper(II) Triflate; Trifluoromethanesulfonic Acid Copper(II) Salt; Cu(OTf)2
CAS Number 34946-82-2
CAT Number RF-PI2078
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C2CuF6O6S2
Molecular Weight 361.67  
Water Solubility Soluble in Water
Sensitivity Hygroscopic
Melting Point ≥300℃
Storage Temp. Inert Atmosphere, Room Temperature
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance Off-White to Light Blue Solid
Purity / Analysis Method >98.0% (Titration) 
Moisture <0.20%
Carbon by Elemental Analysis 6.0~7.1%
Oxygen by Elemental Analysis 25.5~26.9%
ICP Confirms Cu Components Confirmed
Infrared Spectrum Conforms to Structure
Test Standard Enterprise Standard

Package & Storage:

Package25kg/Drum, or according to customer's requirement

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture

Advantages:

1

FAQ:

Application:

Copper(II) Trifluoromethanesulfonate (CAS: 34946-82-2) is usually used as catalyst for Mannich condensation, Annulative amination, Friedel-Crafts reaction, Henry reaction, Hypervalent iodine reagent-mediated preparation of carbazoles, Intramolecular oxidative C-N bond formation for the synthesis of carbazoles, the efficient addition of trimethylsilyl cyanide to carbonyl compounds. Ring-Opening of epoxides and aziridines. Asymmetric conjugate addition of organozinc reagents to α,β-unsaturated ketones. Electrophilic addition of olefins. Asymmetric aziridination of olefins. Asymmetric cycloadditions and aldol condensations. Asymmetric Kharasch oxidation. Asymmetric Michael addition of enamides. Asymmetric O-H or O-R insertion reactions. Enantioselective intramolecular aminooxygenation of alkenes. Enantioselective addition of dialkylzinc reagents to N-acylpyridinium salts. Pd-catalyzed C-H functionalizations of oximes with arylboronic acids. Used as a Lewis acid in the Nazarov cyclization. Catalyst in the diacetoxylation olefins. Catalyst in the meta-selective direct arylation of α-aryl carbonyl compounds. Catalyst in the three-component coupling of amines, aldehydes, and alkynes.  

  • Write your message here and send it to us