Tri-t-butylphosphonium tetrafluoroborate, 99%|15-6000|131274-22-1

Tri-t-butylphosphonium tetrafluoroborate, 99%

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Sku SC15-6000_25_G
US-Strem
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Product Information

Product Name
Tri-t-butylphosphonium tetrafluoroborate, 99%
Brand Name
US-Strem
Product Number
15-6000
CAS
131274-22-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2734635
IUPAC Name
tritert-butylphosphanium tetrafluoroborate
InChI Key
YTJUCJAUJCXFTN-UHFFFAOYSA-O
SMILES
B-(F)(F)(F)F.CC(C)(C)PH+(C(C)(C)C)C(C)(C)C

Application

Technical Notes:
1. Air-stable, non-pyrophoric precursor of the Tri-t-butylphos phine ligand which is used in a variety of catalytic processes.
2.L igand for Suzuki cross-couplings .
3.L igand for Heck Re actions.
4.L igand for Stille Cross-couplings.
5.L igand for a-Arylation and vinylation of arylmandelic acid de rivatives .
6.L igand for direct arylation of hetercycles
7.Synthesis of be nzocyclobutenes by C-H activation.
8.Cross-coupling of Grignard reagents and aryl bromides.
9.Palladium catalyzed annulation of haloanilines.
10Palladium-Catalyzed Acylation.
11. Palladium Catalyzed Carbonylative Heck Reaction.
12. Palladium-catalyzed aminosulfonylation.
13.Palladium-catalyzed intramolecular c -O bond formation .
14. Ruthenium-catalyzed cross-coupling of aldehydes with arylboronic acid.

References Data Source From Pubchem

Development of smartphone-based AIE fluorescence-quenching immunochromatographic sensors for the detection of illicit drugs in various complex sample matrices
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DOI: 10.1007/s00216-025-06106-5

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Publication Date: 2025-04-03
DOI: 10.1038/s41563-025-02199-6

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