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Catalog Number:
28123
CAS Number:
87199-16-4
3-Boronobenzaldehyde
Purity:
≥ 98% (HPLC)
Synonym(s):
3-Formylphenylboronic acid, 3-(Dihydroxyboranyl)benzaldehyde
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Product Information

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.

Synonyms
3-Formylphenylboronic acid, 3-(Dihydroxyboranyl)benzaldehyde
CAS Number
87199-16-4
Purity
≥ 98% (HPLC)
Molecular Formula
C7H7BO3
Molecular Weight
149.94
MDL Number
MFCD00161356
PubChem ID
2734356
Melting Point
120-192 °C
Appearance
Pale yellow powder
Conditions
Store at 0-8°C
General Information
Synonyms
3-Formylphenylboronic acid, 3-(Dihydroxyboranyl)benzaldehyde
CAS Number
87199-16-4
Purity
≥ 98% (HPLC)
Molecular Formula
C7H7BO3
Molecular Weight
149.94
MDL Number
MFCD00161356
PubChem ID
2734356
Melting Point
120-192 °C
Appearance
Pale yellow powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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