COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX

COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX
  • CAS No.:42152-46-5
Other grades of this product :
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
COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX Chemical Properties
Melting point 160 °C (dec.) (lit.)
Fp 45 °F
storage temp. Inert atmosphere,2-8°C
form Powder
color Gray-greenish
InChIKeyOGHGYDFTMBZZJU-UHFFFAOYSA-M
CAS DataBase Reference42152-46-5
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 Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
COPPER(I) TRIFLUOROMETHANESULFONATE BENZENE COMPLEX Usage And Synthesis
Chemical PropertiesGrey-greenish powder
UsesCopper(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 COMPLEX Preparation Products And Raw materials

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