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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)-

5-Hydroxy-2-methylphenylboronic acid

Oc1ccc(c(c1)B(O)O)C Request for Quotation
Chemical Name: 5-Hydroxy-2-methylphenylboronic acid
CAS Number: 1375216-45-7
Product Number: AG0013GQ(AGN-PC-0WABGL)
Synonyms:
MDL No:
Molecular Formula: C7H9BO3
Molecular Weight: 151.9556

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile compound used in chemical synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its primary application lies in Suzuki-Miyaura cross-coupling reactions, where it serves as a boronic acid building block for the construction of various complex organic molecules. By participating in palladium-catalyzed coupling reactions, this compound facilitates the efficient assembly of biaryl structures, which are prevalent in pharmaceuticals, agrochemicals, and materials science. Additionally, (5-Hydroxy-2-methylphenyl)boronic acid demonstrates high reactivity and selectivity, making it a valuable tool for organic chemists seeking to streamline their synthetic routes and access diverse chemical space.