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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, B-(3-methoxy-4-methylphenyl)-

COc1cc(ccc1C)B(O)O Request for Quotation
Chemical Name: Boronic acid, B-(3-methoxy-4-methylphenyl)-
CAS Number: 917757-15-4
Product Number: AG006P2U(AGN-PC-04TKR7)
Synonyms:
MDL No: MFCD08274479
Molecular Formula: C8H11BO3
Molecular Weight: 165.9821

Identification/Properties

Properties
MP:
192-194°C
BP:
318.3 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boronic acid, B-(3-methoxy-4-methylphenyl)-, is a versatile compound widely used in chemical synthesis. This specific boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura coupling reactions. In these reactions, the boronic acid group reacts with an aryl halide in the presence of a palladium catalyst, leading to the formation of biaryl compounds. This powerful synthetic strategy is crucial in organic chemistry for creating a diverse range of complex molecules, including pharmaceuticals, agrochemicals, and materials. The unique structure of B-(3-methoxy-4-methylphenyl)-boronic acid makes it a valuable building block in designing and synthesizing novel compounds with specific properties and functionalities.