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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)-

(2,3-difluoro-4-methylphenyl)boronic acid

OB(c1ccc(c(c1F)F)C)O Request for Quotation
Chemical Name: (2,3-difluoro-4-methylphenyl)boronic acid
CAS Number: 508235-16-3
Product Number: AG006VPU(AGN-PC-044Q4H)
Synonyms:
MDL No:
Molecular Formula: C7H7BF2O2
Molecular Weight: 171.9371

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
171.938g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
172.051g/mol
Monoisotopic Mass:
172.051g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
156
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


(2,3-Difluoro-4-methylphenyl)boronic acid is a versatile compound widely utilized in chemical synthesis as a valuable building block. Its unique chemical properties make it a crucial reagent in various organic reactions, particularly in the pharmaceutical and agrochemical industries.This compound serves as a key component in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron source to facilitate the formation of carbon-carbon bonds. The introduction of the difluoro and methyl substituents in the aromatic ring enhances the reactivity and selectivity of the compound in coupling reactions, leading to efficient synthesis of diverse biaryl compounds.Moreover, (2,3-Difluoro-4-methylphenyl)boronic acid is instrumental in the preparation of fluorinated organic molecules, which are of great interest in medicinal chemistry and materials science. The presence of fluorine atoms imparts unique physicochemical properties to the synthesized compounds, enhancing their biological activity and stability.Overall, the application of (2,3-Difluoro-4-methylphenyl)boronic acid in chemical synthesis enables the efficient and selective construction of complex organic molecules, making it a valuable tool for researchers in drug discovery, materials development, and other fields requiring precise control over molecular structures.