Potassium 4-methylphenyltrifluoroborate, 98%, Thermo Scientific Chemicals
Element SearchElement SearchStructure SearchStructure Search
Potassium 4-methylphenyltrifluoroborate, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Potassium 4-methylphenyltrifluoroborate, 98%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
1 g
5 g
ChemDexTry the chem dexTM web app
Catalog number L17604.03
also known as L17604-03
Price (USD)/ Each
40.20
-
Add to cart
Quantity:
1 g
Request bulk or custom format
Price (USD)/ Each
40.20
Add to cart
Potassium 4-methylphenyltrifluoroborate, 98%, Thermo Scientific Chemicals
Catalog numberL17604.03
Price (USD)/ Each
40.20
-
Add to cart
Chemical Identifiers
CAS216434-82-1
IUPAC Namepotassium trifluoro(4-methylphenyl)boranuide
Molecular FormulaC7H7BF3K
InChI KeyKRWDYXJWQBTBAH-UHFFFAOYSA-N
SMILES[K+].CC1=CC=C(C=C1)[B-](F)(F)F
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
Assay (HPLC)≥97.5%
FormPowder or crystalline powder or crystals
In Suzuki Cross-Coupling organotrifluoroborates is used as potent boronic acid surrogates.

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
In Suzuki Cross-Coupling organotrifluoroborates is used as potent boronic acid surrogates.

Solubility
Soluble in water.

Notes
Store in cool dry conditions in well sealed containers. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Liang Zhang.; Tianhao Meng.; Jie Wu. Palladium-Catalyzed Suzuki-Miyaura Cross-Couplings of Aryl Tosylates with Potassium Aryltrifluoroborates.J. Org. Chem. 2007, 72 (24), 9346-9349 .
  2. Ana Bellomoa.; David Gonzalez.; Hèlio A. Stefani. Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach.J. Organomet. Chem. 2008, 693 (6),1136-1142 .