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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-ETHYL-6-METHYLPHENYLBORONIC ACID

CCc1cccc(c1B(O)O)C Request for Quotation
Chemical Name: 2-ETHYL-6-METHYLPHENYLBORONIC ACID
CAS Number: 953075-89-3
Product Number: AG003H7C(AGN-PC-0WALKI)
Synonyms:
MDL No:
Molecular Formula: C9H13BO2
Molecular Weight: 164.0093

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (2-Ethyl-6-methylphenyl)boronic acid is a versatile compound widely used as a key building block in chemical synthesis processes. It serves as a valuable reagent in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient formation of carbon-carbon bonds in organic molecules. This compound enables the selective introduction of the (2-Ethyl-6-methylphenyl) group into various target molecules, offering synthetic chemists a powerful tool for creating complex organic structures. Additionally, (2-Ethyl-6-methylphenyl)boronic acid plays a crucial role in medicinal chemistry, agrochemical synthesis, and material science applications, highlighting its broad utility in the field of organic chemistry.