ChemicalBook > Product Catalog > Chemical Reagents > Organic reagents > Sulfonates / Sulfinates salts > COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX
COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX
COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX Basic information
- Product Name:
- COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX
- Synonyms:
-
- TRIFLUOROMETHANESULFONIC ACID COPPER(I) SALT BENZENE COMPLEX
- BIS[COPPER (I) TRIFLUOROMETHANESULFONATE], BENZENE COMPLEX
- COPPER(I) TRIFLATE BENZENE COMPLEX
- COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX
- Trifluoromethanesulfonic acid, copper(I) salt
- copper trifluoromethanesulphonate, compound with benzene (2:1)
- COPPER(I) TRIFLUOROMETHANESULFONATE BENZ ENE COMPLEX, TECH., 90%
- Trifluoromethanesulfonicacidcopper(1)saltbenzenecomplex
- CAS:
- 42152-46-5
- MF:
- C8H6Cu2F6O6S2
- MW:
- 503.34
- EINECS:
- 255-686-6
- Product Categories:
-
- Catalysts for Organic Synthesis
- Classes of Metal Compounds
- Cu (Copper) Compounds
- Homogeneous Catalysts
- Metal Triflates
- Synthetic Organic Chemistry
- Transition Metal Compounds
- Mol File:
- 42152-46-5.mol
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COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX Chemical Properties
- Melting point:
- 160 °C (dec.) (lit.)
- Flash point:
- 45 °F
- storage temp.
- Inert atmosphere,2-8°C
- form
- Powder
- color
- Gray-greenish
- InChIKey
- OGHGYDFTMBZZJU-UHFFFAOYSA-M
- CAS DataBase Reference
- 42152-46-5
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Safety Information
- Hazard Codes
- F
- Risk Statements
- 11-36/37/38
- Safety Statements
- 16-26-36
- RIDADR
- UN 3175 4.1/PG 2
- WGK Germany
- 3
- HazardClass
- 4.1
- PackingGroup
- II
- HS Code
- 29049090
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX Usage And Synthesis
Chemical Properties
Grey-greenish powder
Uses
Copper(I) trifluoromethanesulfonate benzene complex can be used as a catalyst:
- To synthesize enol-esters via copper(I) carboxylate intermediate formation.
- In the enantioselective allylic oxidation of cyclic alkenes.
- To prepare 2,5-disubstituted pyrrolidine derivatives from N-alkenyl, alkynyl and alkyl N-benzoyloxysulfonamides via the sulfonamidyl radical formation.
It can also be used in combination with amino acid-based chiral phosphine ligands to catalyze asymmetric conjugate additions of alkylzincs to acyclic α,β-unsaturated ketones, affording β-alkylcarbonyls in high yield and with excellent enantioselectivity.
COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEXSupplier
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