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Catalog Number:
28123
CAS Number:
87199-16-4
3-Boronobenzaldéhyde
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 3-formylphénylboronique, 3-(dihydroxyboranyl)benzaldéhyde
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Informations sur le produit

3-Boronobenzaldehyde is a versatile compound recognized for its unique properties and applications in various fields, particularly in organic synthesis and medicinal chemistry. This compound, also known as 3-formylphenylboronic acid, features a boron atom that enhances its reactivity, making it an excellent building block for the synthesis of complex organic molecules. Researchers often utilize 3-Boronobenzaldehyde in the development of pharmaceuticals, agrochemicals, and advanced materials due to its ability to participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for constructing carbon-carbon bonds.

In addition to its synthetic utility, 3-Boronobenzaldehyde has shown promise in the field of sensor technology, where it can be employed to create highly selective sensors for detecting various analytes. Its unique boronic acid functionality allows for the formation of reversible covalent bonds with diols, making it particularly useful in the design of biosensors and chemical sensors. The compound's stability and reactivity make it a valuable asset for researchers and industry professionals looking to innovate in organic synthesis and sensor development.

Numéro CAS 
87199-16-4
Formule moléculaire
C7H7BO3
Poids moléculaire 
149.94
Point de fusion 
120-192 °C
Informations générales
Numéro CAS 
87199-16-4
Formule moléculaire
C7H7BO3
Poids moléculaire 
149.94
Point de fusion 
120-192 °C
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-Boronobenzaldehyde is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals, allowing for the creation of complex structures efficiently.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds. This application is crucial in the production of biaryl compounds, widely used in drug development.
  • Fluorescent Probes: Researchers utilize 3-Boronobenzaldehyde in the design of fluorescent probes for biological imaging, enhancing the ability to visualize cellular processes in real-time.
  • Material Science: This compound is applied in the development of advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings, providing improved performance characteristics.
  • Chemical Sensors: It is also employed in the fabrication of chemical sensors, particularly for detecting specific analytes, which is vital in environmental monitoring and safety applications.

Citations