1. Home
  2. [6-(2-fluorophenoxy)pyridin-3-yl]boronic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

[6-(2-fluorophenoxy)pyridin-3-yl]boronic acid

Fc1ccccc1Oc1ccc(cn1)B(O)O Request for Quotation
Chemical Name: [6-(2-fluorophenoxy)pyridin-3-yl]boronic acid
CAS Number: 1105663-76-0
Product Number: AG007USW(AGN-PC-0J0YEA)
Synonyms:
MDL No:
Molecular Formula: C11H9BFNO3
Molecular Weight: 233.0035

Identification/Properties

Computed Properties
Molecular Weight:
233.005g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
233.066g/mol
Monoisotopic Mass:
233.066g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
245
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The (6-(2-Fluorophenoxy)pyridin-3-yl)boronic acid is a versatile compound widely utilized in chemical synthesis as a key building block. Its unique structure and properties make it an essential component in the development of various pharmaceuticals, agrochemicals, and materials. In organic synthesis, this compound serves as a valuable reagent for Suzuki-Miyaura cross-coupling reactions, enabling the efficient formation of carbon-carbon bonds. Additionally, its boronic acid functionality allows for the selective functionalization of aromatic compounds, further expanding its utility in the creation of complex molecules. Furthermore, (6-(2-Fluorophenoxy)pyridin-3-yl)boronic acid has been employed in the synthesis of novel heterocyclic structures and advanced materials, highlighting its importance in the field of chemical research and development.