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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, [2,2'-bipyridine]-4,4'-diylbis-

OB(c1ccnc(c1)c1nccc(c1)B(O)O)O Request for Quotation
Chemical Name: Boronic acid, [2,2'-bipyridine]-4,4'-diylbis-
CAS Number: 159614-36-5
Product Number: AG001R8I(AGN-PC-0Q7P93)
Synonyms:
MDL No:
Molecular Formula: C10H10B2N2O4
Molecular Weight: 243.8194

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
243.82g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
244.083g/mol
Monoisotopic Mass:
244.083g/mol
Topological Polar Surface Area:
107A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
244
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


[2,2'-Bipyridine]-4,4'-diyldiboronic acid is a versatile compound widely used in chemical synthesis as a key building block for the construction of complex organic molecules. This compound plays a crucial role in cross-coupling reactions, specifically in the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure containing boronic acid groups enables it to participate in Suzuki-Miyaura coupling reactions, allowing for the efficient synthesis of various functionalized biaryl compounds. Additionally, [2,2'-Bipyridine]-4,4'-diyldiboronic acid serves as a valuable ligand in metal-catalyzed reactions, facilitating challenging transformations with high efficiency and selectivity. Its ability to coordinate with transition metals enhances catalytic processes, making it an essential component in modern organic synthesis strategies.