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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-3-(methoxycarbonyl)phenyl)boronic acid

COC(=O)c1cccc(c1F)B(O)O Request for Quotation
Chemical Name: (2-Fluoro-3-(methoxycarbonyl)phenyl)boronic acid
CAS Number: 1315476-07-3
Product Number: AG000ZEI(AGN-PC-0WNOQC)
Synonyms:
MDL No:
Molecular Formula: C8H8BFO4
Molecular Weight: 197.9561

Identification/Properties

Computed Properties
Molecular Weight:
197.956g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
198.05g/mol
Monoisotopic Mass:
198.05g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
212
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


The chemical compound (2-Fluoro-3-(methoxycarbonyl)phenyl)boronic acid is a valuable tool in chemical synthesis due to its versatile applications. This compound is commonly used as a building block in the production of pharmaceuticals, agrochemicals, and materials with specific properties.In chemical synthesis, (2-Fluoro-3-(methoxycarbonyl)phenyl)boronic acid serves as a key reagent in Suzuki-Miyaura cross-coupling reactions. This reaction allows for the formation of carbon-carbon bonds by coupling an aryl or vinyl boronic acid with an organic halide or pseudohalide in the presence of a palladium catalyst. This versatile reaction is widely used in organic synthesis to construct complex molecules efficiently.Additionally, (2-Fluoro-3-(methoxycarbonyl)phenyl)boronic acid can be used in the synthesis of fluorinated organic compounds. The fluorine atom in the structure provides unique properties that can enhance the bioactivity or physicochemical characteristics of the resulting molecules. This makes it a valuable building block in drug discovery and materials science.Overall, the compound (2-Fluoro-3-(methoxycarbonyl)phenyl)boronic acid plays a crucial role in modern organic synthesis by enabling the construction of complex molecules and facilitating the preparation of fluorinated compounds with diverse applications.