Trityl tetrakis(pentafluorophenyl)borate

CAS : 136040-19-2

Ref. 3D-FT102373

Informations sur le produit

• Nom: Trityl tetrakis(pentafluorophenyl)borate
• Synonymes: Benzene, pentafluoro-, boron complex, Borate(1-), tetrakis(pentafluorophenyl)-, triphenylmethylium, F 20, F 20 (catalyst), Methylium, triphenyl-, tetrakis(2,3,4,5,6-pentafluorophenyl)borate(1-) (1:1), Methylium, triphenyl-, tetrakis(pentafluorophenyl)borate(1-) (1:1), Ph3CB(C6F5)4, Phenylcarbenium tetrakis(pentafluorophenyl)borate, Substituted alkyl salt of halogenated organoborate, Tbf 20, Triphenylcarbenium tetra(perfluorophenyl)borate, Triphenylcarbenium tetrakis(pentafluorophenyl)borate, Triphenylcarbenium tetrakis(pentafluorophenyl)borate(1-), Triphenylcarbenium tetrakis(perfluorophenyl)borate, Triphenylcarbonium tetra(pentafluorophenyl)borate, Triphenylcarbonium tetrakis(pentafluorophenyl)borate, Triphenylcarbonium tetrakis(pentafluorophenyl)borate(1-), Triphenylcarbonium tetrakis(perfluorophenyl)borate, Triphenylmethyl tetrakis(pentafluorophenyl)borate, Triphenylmethylium tetrakis(2,3,4,5,6-pentafluorophenyl)borate, Triphenylmethylium tetrakis(pentafluorophenyl)borate, Triphenylmethylium tetrakis(pentafluorophenyl)borate(1-), Triphenylmethylium tetrakis(perfluorophenyl)borate, Trityl tetra(perfluorophenyl)borate, Trityl tetrakis(perfluorophenyl)borate, Tritylium tetrakis(pentafluorophenyl)borate, [CPh₃][B(C₆F₅)₄], [Ph3C][B(C6F5), TRITYL(TETRAPENTAFLUOROPHENYL)BORATE 98+%, Methylium, triphenyl-, tetrakis(pentafluorophenyl)borate(1-), TRITYL(TETRAPENTAFLUOROPHENYL)BORATE, METHYLIUM,TRIPHENYL-,TETRAKIS(PENTAFLUOROPHENYL)BORATE(1-), TRIPHENYLMETHYLCARBENIUM TETRAKIS(PENTAFLUOROPHENYL)BORATE, Trityltetra(pentafluorophenyl)borate, min. 98%, Trityltetrakis(pentafluorophenyl)borat, Trityltetra(pentafluorophenyl)borate,min.98%

Description

Trityl tetrakis(pentafluorophenyl)borate is a reactive metal-organic compound that is used as an efficient and stereoselective method for the synthesis of trifluoromethanesulfonic acid. The Friedel-Crafts reaction involves the reaction of a halogenated aromatic compound with an alkyl or aryl group, which can be activated by a cocatalyst such as zinc chloride. Trityl tetrakis(pentafluorophenyl)borate has been shown to produce trifluoromethanesulfonic acid in high yields when reacted with zirconium dichloride and a cocatalyst of triethylsilane. This method can be used to synthesize various disaccharides, including maltose, cellobiose, and sucrose.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 922.36 g/mol
• Formule: C₄₃H₁₅BF₂₀
• Degré de pureté: Min. 95%