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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, [4-(benzoylamino)phenyl]-

OB(c1ccc(cc1)NC(=O)c1ccccc1)O Request for Quotation
Chemical Name: Boronic acid, [4-(benzoylamino)phenyl]-
CAS Number: 397843-80-0
Product Number: AG0077CY(AGN-PC-00GK38)
Synonyms:
MDL No:
Molecular Formula: C13H12BNO3
Molecular Weight: 241.0503

Identification/Properties

Computed Properties
Molecular Weight:
241.053g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
241.091g/mol
Monoisotopic Mass:
241.091g/mol
Topological Polar Surface Area:
69.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
271
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


(4-Benzamidophenyl)boronic acid, commonly known as BBPA, is a versatile and valuable chemical reagent in organic synthesis. This compound is widely used as a building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are crucial in the synthesis of complex organic molecules.In the realm of medicinal chemistry, BBPA is often utilized in the preparation of biologically active compounds due to its ability to form strong and selective bonds with certain functional groups. This makes it a valuable tool for the construction of molecular scaffolds with specific pharmacological properties. Additionally, (4-Benzamidophenyl)boronic acid has found applications in the development of novel molecular sensors and catalysts, showcasing its versatility in a wide range of chemical transformations.Overall, the use of BBPA in chemical synthesis highlights its importance as a key component in the construction of diverse molecular architectures with potential applications in various fields of science and technology.