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Catalog Number:
40294
CAS Number:
932378-94-4
Acide [3,5-bis(éthoxycarbonyl)phényl]boronique
Purity:
97 - 105 % (dosage par titrage)
Documents
$77.92 /200 mg
Taille
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Informations sur le produit

[3,5-Bis(ethoxycarbonyl)phenyl]boronic acid is a versatile compound renowned for its applications in organic synthesis and medicinal chemistry. This boronic acid derivative features two ethoxycarbonyl groups that enhance its reactivity and solubility, making it an excellent candidate for cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Researchers and industry professionals can leverage its unique properties for the development of complex organic molecules, including pharmaceuticals and agrochemicals. Its ability to act as a ligand in various catalytic processes further underscores its importance in synthetic methodologies.

In addition to its synthetic utility, [3,5-Bis(ethoxycarbonyl)phenyl]boronic acid has shown promise in the field of materials science, particularly in the creation of functionalized polymers and advanced materials. The compound's stability and reactivity allow for the design of innovative materials with tailored properties, suitable for applications in electronics and nanotechnology. With its broad range of applications and benefits, this compound is an essential tool for researchers and professionals seeking to enhance their synthetic capabilities and explore new avenues in material development.

Numéro CAS 
932378-94-4
Formule moléculaire
C 12 H 15 BO 6
Poids moléculaire 
266.06
Informations générales
Numéro CAS 
932378-94-4
Formule moléculaire
C 12 H 15 BO 6
Poids moléculaire 
266.06
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

[3,5-Bis(ethoxycarbonyl)phenyl]boronic 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 plays a crucial role in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds, which are essential in creating various organic compounds.
  • Material Science: Used in the development of boron-containing polymers, it enhances the properties of materials, making them suitable for applications in electronics and optics.
  • Bioconjugation: This compound can be employed in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other molecules, which is vital in drug delivery systems.
  • Analytical Chemistry: It is utilized in the preparation of boron-based sensors, which can detect specific analytes, providing valuable tools for environmental monitoring and quality control in various industries.

Citations