1. Home
  2. (2,3-difluoro-6-methoxyphenyl)boronic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-6-methoxyphenyl)boronic acid

COc1ccc(c(c1B(O)O)F)F Request for Quotation
Chemical Name: (2,3-difluoro-6-methoxyphenyl)boronic acid
CAS Number: 957061-21-1
Product Number: AG00H83X(AGN-PC-0L9ZQ4)
Synonyms:
MDL No:
Molecular Formula: C7H7BF2O3
Molecular Weight: 187.9365

Identification/Properties

Properties
BP:
322.4°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
187.937g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
188.046g/mol
Monoisotopic Mass:
188.046g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
170
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

Request for Quotation

Customer Feedback

Chemical Structure


2,3-Difluoro-6-methoxyphenylboronic acid is a versatile compound that finds extensive application in chemical synthesis. As a boronic acid derivative, it serves as a valuable building block in organic reactions, particularly in the field of medicinal and pharmaceutical chemistry. This compound is commonly used as a key intermediate in the synthesis of various biologically active molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its unique combination of the difluoro and methoxy functional groups imparts specific reactivity and properties that are crucial for the formation of complex structures.In chemical synthesis, 2,3-Difluoro-6-methoxyphenylboronic acid can participate in Suzuki-Miyaura cross-coupling reactions, where it acts as a coupling partner with suitable aryl halides or pseudohalides. This enables the construction of aromatic compounds with precision and control over the desired substitution pattern.Additionally, this compound can be utilized in transition metal-catalyzed C-H activation reactions to introduce the difluoro-phenyl motif into organic molecules. Such transformations are valuable in streamlining synthetic pathways and enhancing the efficiency of molecule assembly.Overall, the strategic incorporation of 2,3-Difluoro-6-methoxyphenylboronic acid in chemical synthesis enables chemists to access diverse molecular architectures with specific fluorinated and methoxy functionalities, making it an indispensable tool for the synthesis of complex compounds with potential applications in various industries.