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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)-

(6-methoxy-1-benzofuran-2-yl)boronic acid

COc1ccc2c(c1)oc(c2)B(O)O Request for Quotation
Chemical Name: (6-methoxy-1-benzofuran-2-yl)boronic acid
CAS Number: 952737-54-1
Product Number: AG00IMMQ(AGN-PC-08VKMK)
Synonyms:
MDL No:
Molecular Formula: C9H9BO4
Molecular Weight: 191.9764

Identification/Properties

Computed Properties
Molecular Weight:
191.977g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
192.059g/mol
Monoisotopic Mass:
192.059g/mol
Topological Polar Surface Area:
62.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
199
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 (6-Methoxybenzofuran-2-yl)boronic acid, also known as $name$, is a versatile and widely utilized compound in chemical synthesis. As a boronic acid derivative, $name$ is renowned for its ability to participate in various C-C and C-X bond formation reactions through Suzuki-Miyaura cross-coupling reactions, making it an indispensable component in the toolbox of organic chemists. This compound serves as a key building block for the construction of complex organic molecules in pharmaceuticals, agrochemicals, and materials science. Its unique structural features enable precise manipulation of molecular architectures, facilitating the synthesis of diverse drug candidates, natural products, and advanced materials. Additionally, the capability of $name$ to functionalize aromatic systems with high efficiency and selectivity further highlights its significance in modern organic chemistry practices. By harnessing the reactivity of (6-Methoxybenzofuran-2-yl)boronic acid, chemists can access novel chemical entities and drive innovation in the field of synthetic chemistry.