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Catalog Number:
40212
CAS Number:
313545-31-2
Acide 4-éthoxy-2-méthylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-éthoxy-2-méthylbenzèneboronique
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$66.80 /1G
Taille
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Informations sur le produit

4-Ethoxy-2-methylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure allows for selective functionalization, which is particularly beneficial in the development of pharmaceuticals and agrochemicals. Researchers appreciate its role in the synthesis of complex organic molecules, including biologically active compounds, due to its high reactivity and compatibility with various reaction conditions.

In addition to its synthetic applications, 4-Ethoxy-2-methylphenylboronic acid has shown potential in the field of materials science, particularly in the development of advanced polymers and nanomaterials. Its ability to participate in boron-mediated reactions opens avenues for innovative applications in sensor technology and drug delivery systems. With its favorable properties and broad applicability, this compound stands out as a valuable tool for researchers and industry professionals seeking to enhance their synthetic methodologies and explore new frontiers in chemical research.

Numéro CAS 
313545-31-2
Formule moléculaire
C 9 H 13 BO 3
Poids moléculaire 
180.01
Point de fusion 
168 °C (lit.)
Informations générales
Numéro CAS 
313545-31-2
Formule moléculaire
C 9 H 13 BO 3
Poids moléculaire 
180.01
Point de fusion 
168 °C (lit.)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

4-Ethoxy-2-methylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in the production of various organic compounds.
  • Bioconjugation: The boronic acid functional group allows for selective binding to diols, making it useful in bioconjugation techniques for drug delivery systems and targeted therapies.
  • Sensor Development: This chemical can be employed in the creation of sensors for detecting glucose and other biomolecules, benefiting the medical diagnostics industry.
  • Material Science: It is also applied in the development of advanced materials, such as polymers and nanomaterials, enhancing their properties for various industrial applications.

Citations