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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)-

(3-fluoro-4-nitrophenyl)boronic acid

OB(c1ccc(c(c1)F)[N+](=O)[O-])O Request for Quotation
Chemical Name: (3-fluoro-4-nitrophenyl)boronic acid
CAS Number: 1350451-69-2
Product Number: AG007LJZ(AGN-PC-0J2C39)
Synonyms:
MDL No:
Molecular Formula: C6H5BFNO4
Molecular Weight: 184.9176

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-fluoro-4-nitrophenylboronic acid is a versatile and valuable chemical reagent commonly used in various chemical synthesis applications. In organic chemistry, it serves as a precursor in the synthesis of biologically active compounds, pharmaceuticals, and agrochemicals. Particularly, this compound is known for its utility in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid building block to form carbon-carbon bonds. This reaction is widely used in the creation of complex organic molecules, making 3-fluoro-4-nitrophenylboronic acid a valuable tool for medicinal chemistry and material science research. Additionally, this compound can also be employed as a ligand in metal-catalyzed transformations, further expanding its role in modern organic synthesis strategies.