Product Name:Potassium benzofuran-2-yltrifluoroborate

IUPAC Name:potassium (1-benzofuran-2-yl)trifluoroboranuide

CAS:929626-27-7
Molecular Formula:C8H5BF3KO
Purity:95%
Catalog Number:CM219092
Molecular Weight:224.03

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Product Details

CAS NO:929626-27-7
Molecular Formula:C8H5BF3KO
Melting Point:-
Smiles Code:F[B-](F)(C1=CC2=CC=CC=C2O1)F.[K+]
Density:
Catalog Number:CM219092
Molecular Weight:224.03
Boiling Point:
MDL No:MFCD11052671
Storage:Store at 2-8°C.

Category Infos

Borates
Borates are classified as critical materials, they are the main source of boron and have a variety of industrial applications. Organic trifluoroborate is stable to heat, air and humidity, and is a very convenient crystalline boric acid compound. Since it has a tetra-coordinated boronic acid structure after the substitution of fluorine, it does not exhibit Lewis acidity and is stable to oxidation conditions. In addition, it can be regarded as the protector of boronic acid and boronic acid ester, which can be converted into each other. The compound can generally exist stably in organic solvents, but will decompose in protic solvents to liberate trivalent boron, so it can be directly used as a substrate for Suzuki coupling. The difference between trifluoroborate and boric acid is that it must exist in a monomeric form, so the equivalent weight can be closely controlled.
Benzofurans
Benzofuran is an aromatic heterocyclic organic compound with the chemical formula C8H6O. It is a colorless oily liquid at room temperature with an aromatic odor. Benzofuran can be volatilized with water vapor and can be decomposed by potassium permanganate and other oxidants. It is an intermediate for the preparation of amiodarone and indene resin. Benzofuran derivatives are important pharmaceutical intermediates.
Benzofuran | C8H6O | CID 9223 -Chemenu
Benzofuran | C8H6O | CID 9223 |Where to Buy Benzofurans
Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings. This colourless liquid is a component of coal tar.Benzofuran is extracted from coal tar. It is also obtained by dehydrogenation of 2-ethylphenol.

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