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Copper(II) trifluoromethanesulfonate, 98%, Thermo Scientific Chemicals
82.01 - 819.08
Chemische identificatiekenmerken
CAS | 34946-82-2 |
---|---|
Moleculaire formule | CHCuF3O3S |
Molecular Weight (g/mol) | 213.617 |
MDL-nummer | MFCD00077492 |
InChI Key | GZWXEFRPSWBAGC-UHFFFAOYSA-N |
Synoniem | copper; trifluoromethanesulfonic acid |
PubChem CID | 45051791 |
IUPAC Name | copper;trifluoromethanesulfonic acid |
SMILES | C(F)(F)(F)S(=O)(=O)O.[Cu] |
Produktcode | Merk | Aantal | Prijs | Hoeveelheid en beschikbaarheid | |||||
---|---|---|---|---|---|---|---|---|---|
Produktcode | Merk | Aantal | Prijs | Hoeveelheid en beschikbaarheid | |||||
11439736
|
Thermo Scientific Alfa Aesar
B20253.06 |
5 g |
82.01
5 gram |
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11449736
|
Thermo Scientific Alfa Aesar
B20253.14 |
25 g |
262.31
25 gram |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
11459736
|
Thermo Scientific Alfa Aesar
B20253.22 |
100 g |
819.08
100 gram |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
Beschrijving
Copper(II) trifluoromethanesulfonate acts as a catalyst in Diels-Alder reaction and cyclopropanation reactions. It is also used as a reagent for oligosaccharide synthesis. It acts as a Lewis acid. It is also employed in the dimerization of ketone enolates and tetramethylsilane enol ethers. It is used to prepare cis vinylic sulfones and oxazoles from alkynyl sulfones and ketones respectively. Further, it plays an important role for cyclization of dienolates. In addition to this, it is useful for dehydration of alcohols.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsCopper(II) trifluoromethanesulfonate acts as a catalyst in Diels-Alder reaction and cyclopropanation reactions. It is also used as a reagent for oligosaccharide synthesis. It acts as a Lewis acid. It is also employed in the dimerization of ketone enolates and tetramethylsilane enol ethers. It is used to prepare cis vinylic sulfones and oxazoles from alkynyl sulfones and ketones respectively. Further, it plays an important role for cyclization of dienolates. In addition to this, it is useful for dehydration of alcohols.
Solubility
Soluble in water.
Notes
Hygroscopic. Incompatible with strong oxidizing agents.
Chemische identificatiekenmerken
34946-82-2 | |
213.617 | |
GZWXEFRPSWBAGC-UHFFFAOYSA-N | |
45051791 | |
C(F)(F)(F)S(=O)(=O)O.[Cu] |
CHCuF3O3S | |
MFCD00077492 | |
copper; trifluoromethanesulfonic acid | |
copper;trifluoromethanesulfonic acid |
Specificatie
Copper(II) trifluoromethanesulfonate | |
(decomposition) | |
MFCD00077492 | |
4028198 | |
copper; trifluoromethanesulfonic acid | |
GZWXEFRPSWBAGC-UHFFFAOYSA-N | |
copper;trifluoromethanesulfonic acid | |
45051791 | |
98% |
34946-82-2 | |
CHCuF3O3S | |
UN3261 | |
Hygroscopic | |
Soluble in water. | |
C(F)(F)(F)S(=O)(=O)O.[Cu] | |
213.617 | |
361.68 |
Veiligheid en behandeling
GHS H Statement
H314-H318
Causes severe skin burns and eye damage.
Causes serious eye damage.
P260-P264b-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c
H314
missing translation for 'dotInformation' : Transport Hazard Class: 8; Packing Group: III; Proper Shipping Name: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S.
missing translation for 'einecsNumber' : 252-300-8
missing translation for 'tsca' : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only
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