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Hafnium trifluoromethanesulfonate, 98%, Thermo Scientific Chemicals
$192.52 - $600.21
Chemical Identifiers
| CAS | 161337-67-3 |
|---|---|
| Molecular Formula | C4H2F12HfO13S4 |
| Molecular Weight (g/mol) | 792.758 |
| MDL Number | MFCD01321255 |
| InChI Key | XQJOFTWVKHJLHA-UHFFFAOYSA-J |
| Synonym | hafnium iv trifluoromethanesulfonate hydrate, hafnium tetrakis trifluoromethanesulfonate , hydrate |
| PubChem CID | 71433309 |
| IUPAC Name | hafnium(4+);trifluoromethanesulfonate;hydrate |
| SMILES | C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].O.[Hf+4] |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAL1968806
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Thermo Scientific Chemicals
L1968806 |
5 g |
Each for $192.52
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AAL1968814
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Thermo Scientific Chemicals
L1968814 |
25 g |
Each for $600.21
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Description
Hafnium trifluoromethanesulfonate is a recyclable catalyst for the mononitration of o-nitrotoluene. It serves as a catalyst for homogeneous methoxycarbonylation and hydrocarboxylation reactions of phenylacetylene. It is also used as a reactant for direct Friedel-Crafts reactions of chromene hemiacetals, aminomethylation reactions under Lewis acidic conditions and prins-type cyclization reactions. It is also involved in the direct polycondensation of lactic acid. Further, it is used in cationic benzylation reactions, chemoselective thioacetalization and transthioacetalization of carbonyl compounds.
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.
ApplicationsHafnium trifluoromethanesulfonate is a recyclable catalyst for the mononitration of o-nitrotoluene. It serves as a catalyst for homogeneous methoxycarbonylation and hydrocarboxylation reactions of phenylacetylene. It is also used as a reactant for direct Friedel-Crafts reactions of chromene hemiacetals, aminomethylation reactions under Lewis acidic conditions and prins-type cyclization reactions. It is also involved in the direct polycondensation of lactic acid. Further, it is used in cationic benzylation reactions, chemoselective thioacetalization and transthioacetalization of carbonyl compounds.
Solubility
Soluble in methyl cyanide, dicholomethane, dichloroethane, nitromethane, dioxane, terahydrofuran and toluene.
Notes
Incompatible with strong oxidizing agents. Moisture sensitive.
Chemical Identifiers
| 161337-67-3 | |
| 792.758 | |
| XQJOFTWVKHJLHA-UHFFFAOYSA-J | |
| 71433309 | |
| C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].O.[Hf+4] |
| C4H2F12HfO13S4 | |
| MFCD01321255 | |
| hafnium iv trifluoromethanesulfonate hydrate, hafnium tetrakis trifluoromethanesulfonate , hydrate | |
| hafnium(4+);trifluoromethanesulfonate;hydrate |
Specifications
| 161337-67-3 | |
| C4H2F12HfO13S4 | |
| MFCD01321255 | |
| Hygroscopic | |
| Soluble in methyl cyanide,dicholomethane,dichloroethane,nitromethane,dioxane,terahydrofuran and toluene. | |
| C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].O.[Hf+4] | |
| 792.758 | |
| 774.75 | |
| Hafnium trifluoromethanesulfonate |
| >350°C | |
| (CF3SO3)4Hf | |
| 5 g | |
| hafnium iv trifluoromethanesulfonate hydrate, hafnium tetrakis trifluoromethanesulfonate , hydrate | |
| XQJOFTWVKHJLHA-UHFFFAOYSA-J | |
| hafnium(4+);trifluoromethanesulfonate;hydrate | |
| 71433309 | |
| 98% |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only