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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Potassium benzofuran-2-yltrifluoroborate

F[B-](c1cc2c(o1)cccc2)(F)F.[K+] Request for Quotation
Chemical Name: Potassium benzofuran-2-yltrifluoroborate
CAS Number: 929626-27-7
Product Number: AG00GUWO(AGN-PC-0WAEWD)
Synonyms:
MDL No:
Molecular Formula: C8H5BF3KO
Molecular Weight: 224.0292

Identification/Properties

Computed Properties
Molecular Weight:
224.031g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
224.002g/mol
Monoisotopic Mass:
224.002g/mol
Topological Polar Surface Area:
13.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
200
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Potassium benzofuran-2-yltrifluoroborate is a versatile reagent used in organic synthesis for the cross-coupling reactions. This compound plays a crucial role in Suzuki-Miyaura coupling reactions, which is a powerful method for forming carbon-carbon bonds. By combining Potassium benzofuran-2-yltrifluoroborate with aryl halides or pseudohalides in the presence of a palladium catalyst, chemists can efficiently create complex molecular structures. This reaction is widely utilized in the pharmaceutical, agrochemical, and material science industries for the synthesis of various biologically active compounds and functional materials. Furthermore, Potassium benzofuran-2-yltrifluoroborate offers excellent reactivity and compatibility with a wide range of functional groups, making it a valuable tool for the construction of molecular scaffolds with precise control over regio- and stereochemistry.