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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)-

[2-(3-phenylphenyl)phenyl]boronic acid

OB(c1ccccc1c1cccc(c1)c1ccccc1)O Request for Quotation
Chemical Name: [2-(3-phenylphenyl)phenyl]boronic acid
CAS Number: 1133796-50-5
Product Number: AG0008CS(AGN-PC-03Y9GP)
Synonyms:
MDL No:
Molecular Formula: C18H15BO2
Molecular Weight: 274.1215

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


[1,1':3',1''-Terphenyl]-2-ylboronic acid is a versatile and valuable reagent in chemical synthesis. It is commonly used as a key building block in the synthesis of various organic compounds, particularly in the field of organic chemistry. This boronic acid derivative is utilized as a coupling agent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aryl groups under mild reaction conditions. Furthermore, its high reactivity and stability make it a preferred choice for constructing complex molecular architectures with precision and efficiency. The unique structural properties of [1,1':3',1''-Terphenyl]-2-ylboronic acid make it an essential tool for organic chemists seeking to synthesize diverse molecules for applications in pharmaceuticals, materials science, and other chemical industries.