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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, (3-fluoro-4-hydroxyphenyl)-

OB(c1ccc(c(c1)F)O)O Request for Quotation
Chemical Name: Boronic acid, (3-fluoro-4-hydroxyphenyl)-
CAS Number: 182344-14-5
Product Number: AG0023OB(AGN-PC-03X8LI)
Synonyms:
MDL No: MFCD06659838
Molecular Formula: C6H6BFO3
Molecular Weight: 155.9194

Identification/Properties

Properties
MP:
252-256 °C
BP:
331.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
155.919g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
156.039g/mol
Monoisotopic Mass:
156.039g/mol
Topological Polar Surface Area:
60.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
133
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


(3-Fluoro-4-hydroxyphenyl)boronic acid is a versatile compound widely used in organic synthesis. It is a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and materials due to its unique properties and reactivity. This compound plays a crucial role in Suzuki coupling reactions, where it serves as a boronic acid source for the cross-coupling with organic halides or triflates. Additionally, it can be employed in transition metal-catalyzed C-H activation reactions to construct complex chemical structures efficiently. The presence of both a hydroxyl group and a fluorine atom on the phenyl ring offers opportunities for further functionalization, allowing for the synthesis of diverse molecular scaffolds with specific desired properties. Furthermore, (3-Fluoro-4-hydroxyphenyl)boronic acid has found applications in the development of novel materials and in medicinal chemistry for the design and synthesis of potential drug candidates.