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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, (2,3-difluoro-4-methoxyphenyl)-

COc1ccc(c(c1F)F)B(O)O Request for Quotation
Chemical Name: Boronic acid, (2,3-difluoro-4-methoxyphenyl)-
CAS Number: 170981-41-6
Product Number: AG00APVU(AGN-PC-04Z0WT)
Synonyms:
MDL No: MFCD07368234
Molecular Formula: C7H7BF2O3
Molecular Weight: 187.9365

Identification/Properties

Properties
BP:
304.3°C at 760 mmHg
Storage:
Keep in dry area;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

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Chemical Structure


The (2,3-Difluoro-4-methoxyphenyl)boronic acid is a versatile compound widely used in chemical synthesis as a valuable building block. It serves as an essential reagent in the field of organic chemistry, particularly in coupling reactions such as Suzuki-Miyaura cross-coupling. This compound plays a crucial role in the synthesis of various biologically active molecules, pharmaceuticals, agrochemicals, and materials. Its unique structure, combining the properties of fluorine and methoxy groups with the boronic acid functionality, allows for efficient and selective C-C bond formation. This enables chemists to construct complex molecular structures with high precision and control, making it a valuable tool in modern synthetic chemistry.