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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'-methyl[1,1'-biphenyl]-4-yl)-

Cc1ccccc1c1ccc(cc1)B(O)O Request for Quotation
Chemical Name: Boronic acid, (2'-methyl[1,1'-biphenyl]-4-yl)-
CAS Number: 491595-36-9
Product Number: AG00DK8N(AGN-PC-03X8M3)
Synonyms:
MDL No:
Molecular Formula: C13H13BO2
Molecular Weight: 212.0521

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
212.055g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
212.101g/mol
Monoisotopic Mass:
212.101g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
212
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2'-Methyl-[1,1'-biphenyl]-4-yl)boronic acid, a versatile compound widely used in chemical synthesis, serves as a key building block in organic chemistry transformations. With its unique structure and reactivity, this boronic acid derivative is employed in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds efficiently. Additionally, it finds application as a valuable reagent in the synthesis of biaryl compounds, pharmaceutical intermediates, and functional materials. Its ability to undergo selective Suzuki coupling reactions makes it an indispensable tool for the construction of complex molecular structures in drug discovery and material science research.