Thermo Scientific Chemicals

Hafnium trifluoromethanesulfonate, 98%, Thermo Scientific Chemicals

Catalog number: L19688.14
25 g, Each
Thermo Scientific Chemicals

Hafnium trifluoromethanesulfonate, 98%, Thermo Scientific Chemicals

Catalog number: L19688.14
25 g, Each
Quantity
Catalog number: L19688.14
also known as L19688-14
Price (USD)
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Chemical Identifiers

CAS
161337-67-3
IUPAC Name
hafnium(4+) hydrate tetratrifluoromethanesulfonate
Molecular Formula
C4H2F12HfO13S4
InChI Key
XQJOFTWVKHJLHA-UHFFFAOYSA-J
SMILES
O.[Hf+4].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F
Assay (unspecified)
>97.5%
Elemental Analysis
Fluorine: 28.85-29.44%
Appearance (Color)
White to yellow
Form
Powder

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.

Applications
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.

Solubility
Soluble in methyl cyanide, dicholomethane, dichloroethane, nitromethane, dioxane, terahydrofuran and toluene.

Notes
Incompatible with strong oxidizing agents. Moisture sensitive.
RUO – Research Use Only

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