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Catalog Number:
40346
CAS Number:
850568-59-1
Acide 4-éthoxy-3,5-diméthylphénylboronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-éthoxy-3,5-diméthylbenzèneboronique
Documents
$45.37 /1G
Taille
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Informations sur le produit

4-Ethoxy-3,5-dimethylphenylboronic acid is a versatile boronic acid derivative with significant applications in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its unique structure, featuring an ethoxy group and two methyl substituents, enhances its reactivity and selectivity, allowing researchers to develop a wide range of pharmaceuticals and agrochemicals with improved efficacy and reduced side effects.

In addition to its role in synthetic chemistry, 4-Ethoxy-3,5-dimethylphenylboronic acid is also utilized in the development of sensors and materials due to its boron functionality, which can interact with various substrates. This compound's stability and ease of handling make it an attractive choice for both academic and industrial applications. Whether you are involved in drug discovery or materials science, this boronic acid can provide the necessary building blocks for innovative solutions.

Numéro CAS 
850568-59-1
Formule moléculaire
C 10 H 15 BO 3
Poids moléculaire 
194.04
Point de fusion 
211 °C (lit.)
Informations générales
Numéro CAS 
850568-59-1
Formule moléculaire
C 10 H 15 BO 3
Poids moléculaire 
194.04
Point de fusion 
211 °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-3,5-dimethylphenylboronic 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, allowing for the formation of carbon-carbon bonds, which is essential in creating diverse chemical libraries for drug discovery.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation processes for developing targeted drug delivery systems.
  • Sensor Development: This compound can be employed in the fabrication of chemical sensors, particularly for detecting glucose levels, benefiting the medical diagnostics industry.
  • Material Science: It is also applied in the development of advanced materials, such as polymers that exhibit unique properties, enhancing performance in various industrial applications.

Citations