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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)-

(2-fluoro-3-iodophenyl)boronic acid

OB(c1cccc(c1F)I)O Request for Quotation
Chemical Name: (2-fluoro-3-iodophenyl)boronic acid
CAS Number: 1016231-39-2
Product Number: AG000503(AGN-PC-00UQFV)
Synonyms:
MDL No:
Molecular Formula: C6H5BFIO2
Molecular Weight: 265.8166

Identification/Properties

Properties
MP:
238-243 °C(lit.)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
265.817g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
265.941g/mol
Monoisotopic Mass:
265.941g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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

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Chemical Structure


(2-Fluoro-3-iodophenyl)boronic acid is a versatile compound widely used in chemical synthesis as a key building block in the formation of various organic molecules. This compound plays a crucial role in cross-coupling reactions, particularly in palladium-catalyzed processes such as Suzuki-Miyaura coupling, which allows for the selective formation of carbon-carbon bonds.In chemical synthesis, (2-Fluoro-3-iodophenyl)boronic acid serves as a valuable reagent for the preparation of pharmaceuticals, agrochemicals, and materials with important properties. Its unique structure containing both fluorine and iodine atoms enables the selective introduction of these functional groups into target molecules, making it an essential tool for the creation of diverse chemical structures.Furthermore, the presence of the boronic acid moiety in this compound allows for further functionalization through various transformations, leading to the synthesis of complex molecules with high efficiency and selectivity. Its compatibility with a wide range of reaction conditions and substrates makes it a highly sought-after reagent in the field of organic chemistry.