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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, (4-fluoro-2-formylphenyl)-

O=Cc1cc(F)ccc1B(O)O Request for Quotation
Chemical Name: Boronic acid, (4-fluoro-2-formylphenyl)-
CAS Number: 825644-26-6
Product Number: AG008K98(AGN-PC-04XHE2)
Synonyms:
MDL No:
Molecular Formula: C7H6BFO3
Molecular Weight: 167.9301

Identification/Properties

Computed Properties
Molecular Weight:
167.93g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
168.039g/mol
Monoisotopic Mass:
168.039g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile chemical compound used in organic synthesis, specifically known for its application in cross-coupling reactions. (4-Fluoro-2-formylphenyl)boronic acid is a key reagent for the introduction of the 4-fluoro-2-formylphenyl group in a variety of chemical reactions. It serves as a valuable building block for the construction of complex molecules in the field of medicinal chemistry, agrochemicals, and material science. This compound is particularly useful in Suzuki-Miyaura coupling reactions, where it acts as a boronate ester to form carbon-carbon bonds with various aryl halides and vinyl halides. The presence of the fluoro group enhances the reactivity and selectivity of the compound, making it an important tool for chemists seeking to create novel structures with specific functionalities. By incorporating (4-Fluoro-2-formylphenyl)boronic acid into their synthetic routes, researchers can access a wide range of biologically active compounds and functional materials, driving innovation in the field of organic chemistry.