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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-4-nitrophenylboronic acid

OB(c1ccc(cc1F)[N+](=O)[O-])O Request for Quotation
Chemical Name: 2-Fluoro-4-nitrophenylboronic acid
CAS Number: 1436608-93-3
Product Number: AG00AQH6(AGN-PC-0WA6PA)
Synonyms:
MDL No:
Molecular Formula: C6H5BFNO4
Molecular Weight: 184.9176

Identification/Properties

Computed Properties
Molecular Weight:
184.917g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
185.03g/mol
Monoisotopic Mass:
185.03g/mol
Topological Polar Surface Area:
86.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
198
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-4-nitrophenylboronic acid is a versatile compound widely used in chemical synthesis for its unique properties. In organic chemistry, this compound serves as a valuable building block for the construction of various complex molecules due to its ability to participate in a variety of important chemical reactions.One key application of 2-Fluoro-4-nitrophenylboronic acid is its use in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by a palladium catalyst, allows for the formation of new carbon-carbon bonds between an aryl or vinyl boronic acid derivative and an organic halide or pseudohalide. By incorporating 2-Fluoro-4-nitrophenylboronic acid as one of the coupling partners, chemists can efficiently create biaryl or polyaryl compounds with tailored substitution patterns.Furthermore, 2-Fluoro-4-nitrophenylboronic acid can also be utilized in transition metal-catalyzed C-H activation reactions. This methodology enables the direct functionalization of C-H bonds in organic molecules, providing a more atom-economical and direct route to introducing desired functional groups. By using 2-Fluoro-4-nitrophenylboronic acid as a directing group or as a substrate, chemists can access structurally diverse compounds with high efficiency.Overall, the application of 2-Fluoro-4-nitrophenylboronic acid in chemical synthesis offers synthetic chemists a valuable tool for creating complex molecules and designing novel compounds with specific functionalities. Its versatile reactivity and compatibility with various synthetic methodologies make it a valuable asset in the toolbox of synthetic organic chemists.