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Triphenylcarbenium tetrafluoroborate, 97%, Thermo Scientific Chemicals

Catalog Number p-7020855
Click to view available options
Quantity:
10 g
50 g
250 g
341-02-6
C19H15BF4
330.133
MFCD00013120
VQXBOEYKSVVPSP-UHFFFAOYSA-N
triphenylcarbenium tetrafluoroborate, trityl tetrafluoroborate, tritylium tetrafluoroborate, triphenylmethylium tetrafluoroborate, diphenylmethylbenzene tetrafluoroborate, trityl fluoroborate, triphenylmethyl fluoroborate, triphenylcarbonium tetrafluoroborate, methylium, triphenyl-, tetrafluoroborate 1-, methylium, triphenyl-, tetrafluoroborate 1-1:1
2723955
diphenylmethylbenzene;tetrafluoroborate
[B-](F)(F)(F)F.C1=CC=C(C=C1)[C+](C2=CC=CC=C2)C3=CC=CC=C3
341-02-6
C19H15BF4
330.133
MFCD00013120
VQXBOEYKSVVPSP-UHFFFAOYSA-N
triphenylcarbenium tetrafluoroborate, trityl tetrafluoroborate, tritylium tetrafluoroborate, triphenylmethylium tetrafluoroborate, diphenylmethylbenzene tetrafluoroborate, trityl fluoroborate, triphenylmethyl fluoroborate, triphenylcarbonium tetrafluoroborate, methylium, triphenyl-, tetrafluoroborate 1-, methylium, triphenyl-, tetrafluoroborate 1-1:1
2723955
diphenylmethylbenzene;tetrafluoroborate
[B-](F)(F)(F)F.C1=CC=C(C=C1)[C+](C2=CC=CC=C2)C3=CC=CC=C3

It is applied in the abstraction of the-H atom of alcohols and their O-substituted derivatives results in oxidation to the ketones and in the oxidation of TMS ethers to ketones, secondary alcohols to ketones, and secondary diols to ?-hydroxy ketones. It is applied as a reactant involved in the synthesis of substituted dihydroazulene photo switches, carbene-based Lewis pairs for hydrogen activation, 1,3-Dipolar cycloaddition reactions for preparation of α-amino-β-hydroxy esters, oxidation of allenic compounds, Mukaiyama aldol addition reactions and ionic hydrogenation as a counteranion and ligand source.

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
It is applied in the abstraction of the ɑ-H atom of alcohols and their O-substituted derivatives results in oxidation to the ketones and in the oxidation of TMS ethers to ketones, secondary alcohols to ketones, and secondary diols to ɑ-hydroxy ketones. It is applied as a reactant involved in the synthesis of substituted dihydroazulene photo switches, carbene-based Lewis pairs for hydrogen activation, 1,3-Dipolar cycloaddition reactions for preparation of α-amino-β-hydroxy esters, oxidation of allenic compounds, Mukaiyama aldol addition reactions and ionic hydrogenation as a counteranion and ligand source.

Solubility
Insoluble in water. Soluble in methanol.

Notes
Moisture sensitive. Store away from bases, water/moisture, heat and oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition. Store under inert gas. Keep it refrigerated.
TRUSTED_SUSTAINABILITY
Melting Point ∼207°C (decomposition)
Odor Odorless
Linear Formula (C6H5)3CBF4
Quantity 10 g
UN Number UN3261
Beilstein 5085649
Sensitivity Moisture sensitive
Solubility Information Insoluble in water. Soluble in methanol.
Formula Weight 330.13
Percent Purity 98%
Chemical Name or Material Triphenylcarbenium tetrafluoroborate
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