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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)-

Boronic acid, (2-fluoro-5-iodophenyl)-

Ic1ccc(c(c1)B(O)O)F Request for Quotation
Chemical Name: Boronic acid, (2-fluoro-5-iodophenyl)-
CAS Number: 866683-41-2
Product Number: AG003HA9(AGN-PC-00UQFU)
Synonyms:
MDL No:
Molecular Formula: C6H5BFIO2
Molecular Weight: 265.8166

Identification/Properties

Properties
MP:
>230°C(lit.);
Storage:
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-5-iodophenylboronic acid is a versatile compound commonly used in organic synthesis as a key building block. Its unique chemical properties make it valuable in various chemical processes, particularly in the field of pharmaceuticals and agrochemicals.In chemical synthesis, 2-Fluoro-5-iodophenylboronic acid acts as a crucial reagent for Suzuki-Miyaura cross-coupling reactions. This reaction involves the coupling of an aryl halide or pseudohalide with an aryl or vinyl boronic acid in the presence of a palladium catalyst. By using 2-Fluoro-5-iodophenylboronic acid as one of the reactants, chemists can efficiently form carbon-carbon bonds to construct complex organic molecules with high precision.Furthermore, this compound can also be employed in other types of C-C and C-N bond formation reactions, allowing chemists to access a wide range of substituted aromatic compounds. The presence of both fluorine and iodine atoms in the molecule provides flexibility in introducing diverse functional groups into the final product, enhancing its potential utility in medicinal chemistry and materials science.Overall, the application of 2-Fluoro-5-iodophenylboronic acid in chemical synthesis offers a powerful tool for organic chemists to design and create novel compounds with specific structural and functional properties.