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Catalog Number:
40115
CAS Number:
17933-03-8
Ácido 3-metilfenilborónico
Purity:
97 - 104% (Ensayo por titulación)
Synonym(s):
Ácido 3-metilbencenoborónico, Ácido m -tolilborónico
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Tamaño
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Product Information

3-Methylphenylboronic acid is a versatile organoboron compound widely utilized in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with various substrates, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure allows for selective functionalization of aromatic compounds, which is crucial in the development of pharmaceuticals and agrochemicals. Researchers appreciate its effectiveness in facilitating the formation of carbon-carbon bonds, thereby streamlining synthetic pathways in complex molecule construction.

In addition to its role in organic synthesis, 3-Methylphenylboronic acid has applications in sensor technology and materials science. Its boronic acid functionality enables it to interact with diols, making it useful in the development of glucose sensors and other biosensing applications. The compound's stability and ease of use further enhance its appeal, providing researchers and industry professionals with a reliable tool for innovative applications. Whether in the lab or in industrial settings, 3-Methylphenylboronic acid stands out for its practicality and effectiveness in advancing chemical research and product development.

Synonyms
Ácido 3-metilbencenoborónico, Ácido m -tolilborónico
CAS Number
17933-03-8
Purity
97 - 104% (Ensayo por titulación)
Molecular Formula
C7H9BO2
Molecular Weight
135.96
MDL Number
MFCD00040198
PubChem ID
2733950
Melting Point
160 - 162 °C
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 3-metilbencenoborónico, Ácido m -tolilborónico
CAS Number
17933-03-8
Purity
97 - 104% (Ensayo por titulación)
Molecular Formula
C7H9BO2
Molecular Weight
135.96
MDL Number
MFCD00040198
PubChem ID
2733950
Melting Point
160 - 162 °C
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Methylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the creation of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is essential in Suzuki-Miyaura cross-coupling reactions, allowing researchers to form carbon-carbon bonds efficiently, which is crucial in developing complex organic compounds.
  • Bioconjugation: The ability to form stable bonds with biomolecules makes it valuable in bioconjugation processes, aiding in the development of targeted drug delivery systems.
  • Sensor Development: This chemical is used in the fabrication of sensors for detecting glucose and other analytes, providing significant advancements in medical diagnostics.
  • Material Science: It plays a role in the development of advanced materials, including polymers and nanomaterials, enhancing properties such as conductivity and strength.

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