Nombre del producto:2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester

IUPAC Name:1-[3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1H-pyrazole

CAS:858523-46-3
Fórmula molecular:C16H21BN2O2
Pureza:95%
Número de catálogo:CM363830
Peso molecular:284.17

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Detalles del producto

Núm. De CAS :858523-46-3
Fórmula molecular:C16H21BN2O2
Punto de fusión:-
Código de sonrisas:CC1(C)C(C)(C)OB(C2=CC=C(N3N=CC=C3)C=C2C)O1
Densidad:
Número de catálogo:CM363830
Peso molecular:284.17
Punto de ebullición:
Nº Mdl:MFCD11043445
Almacenamiento:

Category Infos

Pyrazoles
Pyrazoles are organic compounds of the general formula C3H3N2H. It is a five-membered heterocycle consisting of three carbon atoms and two adjacent nitrogen atoms. As an H-bond-donating heterocycle, pyrazole has been used as a more lipophilic and metabolically more stable bioisomer of phenol. Pyrazoles have attracted more and more attention due to their broad spectrum of action and strong efficacy.
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Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Product Overview 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester (MPBPO) is an organic compound that has been studied extensively due to its potential applications in the scientific research field. MPBPO is a colorless, crystalline solid with a molecular weight of 284.17 g/mol. It is a boronic acid derivative and has been found to be a useful reagent in organic synthesis and has been used as a building block in the synthesis of more complex organic compounds.
Synthesis and Application 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95% can be synthesized by reacting 4-methyl-1H-pyrazole-1-boronic acid pinacol ester with 2-chloro-4-methylphenylboronic acid in aqueous acetonitrile. The reaction is carried out at a temperature of 80°C and is completed in a few hours. The reaction mixture is then cooled to room temperature and the product is isolated by filtration. The isolated product is then purified by recrystallization. 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95% has been found to be a useful reagent in organic synthesis and has been used in the synthesis of a variety of organic compounds. It has been used in the synthesis of polymers, pharmaceuticals, and other organic molecules. It has also been used in the synthesis of peptide-based drugs, as well as in the synthesis of peptide-based vaccines. In addition, 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95% has been used in the synthesis of a variety of organometallic compounds, such as cobalt complexes and nickel complexes.
Future Directions There are a number of potential future directions for 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95%. One potential direction is the use of 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95% in the synthesis of peptide-based drugs and vaccines. Additionally, 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95% could be used in the synthesis of organometallic compounds, such as cobalt complexes and nickel complexes. Furthermore, 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95% could be used in the synthesis of polymers and other organic molecules. Additionally, 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95% could be used in the synthesis of enzyme inhibitors, which could be used in the treatment of a variety of diseases. Finally, 2-Methyl-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester, 95% could be used in the synthesis of fluorescent molecules, which could be used in the study of cellular processes and other biological phenomena.