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POTASSIUM BENZYLTRIFLUOROBORATE

Base Information
  • Chemical Name:POTASSIUM BENZYLTRIFLUOROBORATE
  • CAS No.:329976-73-0
  • Molecular Formula:C7H7BF3K
  • Molecular Weight:198.03
  • Hs Code.:29319090
  • Mol file:329976-73-0.mol
POTASSIUM BENZYLTRIFLUOROBORATE

Synonyms:Borate(1-),trifluoro(phenylmethyl)-, potassium, (T-4)- (9CI);

Suppliers and Price of POTASSIUM BENZYLTRIFLUOROBORATE
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Potassium benzyltrifluoroborate
  • 1g
  • $ 90.00
  • SynQuest Laboratories
  • Potassium benzyltrifluoroborate 97%
  • 5 g
  • $ 196.00
  • Sigma-Aldrich
  • Potassium benzyltrifluoroborate 95%
  • 1g
  • $ 146.00
  • Sigma-Aldrich
  • Potassium benzyltrifluoroborate 95%
  • 5g
  • $ 572.00
  • Matrix Scientific
  • Potassium benzyltrifluoroborate 95+%
  • 5g
  • $ 622.00
  • Matrix Scientific
  • Potassium benzyltrifluoroborate 95+%
  • 1g
  • $ 227.00
  • Crysdot
  • Potassium benzyltrifluoroborate 97%
  • 5g
  • $ 127.00
  • Chemenu
  • Potassium benzyltrifluoroborate 95+%
  • 25g
  • $ 426.00
  • Chemenu
  • Potassium benzyltrifluoroborate 95+%
  • 10g
  • $ 204.00
  • Chemenu
  • Potassium benzyltrifluoroborate 95+%
  • 5g
  • $ 116.00
Total 33 raw suppliers
Chemical Property of POTASSIUM BENZYLTRIFLUOROBORATE
Chemical Property:
  • Melting Point:>300 ºC 
  • PSA:0.00000 
  • LogP:2.88210 
  • Storage Temp.:Inert atmosphere,Room Temperature 
Purity/Quality:

99%, *data from raw suppliers

Potassium benzyltrifluoroborate *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Organotrifluoroborate involved in:OxidationRitter-type amidation with nitrilesPhoto-allylation / photo-benzylation of carbonyl compoundsStereoselective nucleophilic additionSuzuki cross-couplingOrganotrifluoroborates as versatile and stable boronic acid surrogates Organotrifluoroborate involved in:? ;Oxidation1,2? ;Ritter-type amidation with nitriles3? ;Photo-allylation / photo-benzylation of carbonyl compounds4? ;Stereoselective nucleophilic addition5? ;Suzuki cross-coupling6Organotrifluoroborates as versatile and stable boronic acid surrogates
Refernces

Metal-organic layers as multifunctional two-dimensional nanomaterials for enhanced photoredox catalysis

10.1021/jacs.9b08956

The research focuses on the development of multifunctional metal-organic layers (MOLs) for enhanced photoredox catalysis. The experiments involved the synthesis and characterization of a specific MOL, Hf12-Ir-Ni, which integrates photosensitizing DBB-Ir-F bridging ligands and catalytically active MBA-Ni capping agents. The reactants used in the synthesis include Hf12-Ir-F, MBA capping agents, and NiCl2 for metalation. Various analytical techniques were employed to characterize the MOLs, such as dynamic light scattering (DLS), powder X-ray diffraction (PXRD), high-resolution TEM (HRTEM), 1H NMR spectroscopy, thermogravimetric analysis (TGA), UV-Vis and luminescence spectroscopy, X-ray absorption spectroscopy, and inductively coupled plasma-mass spectrometry (ICP-MS). The photocatalytic performance of Hf12-Ir-Ni was evaluated in three significant single-electron transfer (SET) reactions: C-S cross coupling between aryl iodides and thiols, C-O cross coupling between alcohols and aryl bromides, and C-C cross-coupling between potassium benzyltrifluoroborates and aryl bromides. The MOL demonstrated high efficiency in these reactions, with high turnover numbers and low catalyst loadings, outperforming homogeneous catalysts. The study also investigated electron transfer rates and photocatalytic reaction rates, showing significant enhancements in intra-MOL electron transfer and reactivity compared to homogeneous systems.

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