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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-[[bis(1-methylethyl)amino]carbonyl]-3-methoxyphenyl]-

COc1cccc(c1C(=O)N(C(C)C)C(C)C)B(O)O Request for Quotation
Chemical Name: Boronic acid, [2-[[bis(1-methylethyl)amino]carbonyl]-3-methoxyphenyl]-
CAS Number: 129112-20-5
Product Number: AG009C21(AGN-PC-01ZVC9)
Synonyms:
MDL No:
Molecular Formula: C14H22BNO4
Molecular Weight: 279.1398

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-(Diisopropylcarbamoyl)-3-methoxyphenyl)boronic acid is a versatile molecule commonly used in chemical synthesis due to its unique properties. This compound serves as an important building block in organic synthesis, specifically in the field of medicinal chemistry and material science. By utilizing the boronic acid moiety, researchers can easily introduce the (2-(Diisopropylcarbamoyl)-3-methoxyphenyl) functional group into various organic molecules, allowing for the creation of novel compounds with enhanced properties.One common application of (2-(Diisopropylcarbamoyl)-3-methoxyphenyl)boronic acid is in Suzuki-Miyaura cross-coupling reactions, a widely employed method in organic chemistry for the formation of carbon-carbon bonds. In this reaction, the boronic acid group acts as a nucleophile, participating in the coupling with aryl halides or pseudohalides under the catalysis of palladium complexes. This enables the synthesis of biaryl compounds, which are prevalent motifs in pharmaceuticals and agrochemicals.Additionally, the (2-(Diisopropylcarbamoyl)-3-methoxyphenyl)boronic acid can be utilized in the construction of heterocycles, such as benzoxazoles or benzothiazoles, through intramolecular Suzuki cross-coupling reactions. These heterocyclic compounds are important structural motifs in drug discovery and materials science, making this application particularly valuable in the synthesis of bioactive molecules and advanced materials.Overall, the (2-(Diisopropylcarbamoyl)-3-methoxyphenyl)boronic acid plays a crucial role in enabling the efficient and selective formation of complex organic molecules, making it an indispensable tool for chemists engaged in the development of new compounds for various applications.