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Catalog Number:
40149
CAS Number:
4151-80-8
4,4'-Biphenyldiboronic acid
Purity:
≥ 95% (Assay by titration)
Synonym(s):
[4-(4-boronophenyl)phenyl]boronic acid
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Product Information

4,4'-Biphenyldiboronic acid is a versatile compound widely recognized for its applications in organic synthesis and materials science. This compound, characterized by its unique biphenyl structure with two boronic acid functional groups, serves as an essential building block in the development of advanced materials, including organic light-emitting diodes (OLEDs) and organic photovoltaics. Its ability to form stable complexes with various substrates enhances its utility in catalysis and sensor technology, making it a valuable resource for researchers and industry professionals alike.

The compound's distinctive properties, such as its high thermal stability and solubility in organic solvents, facilitate its use in a range of chemical reactions, including Suzuki-Miyaura cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules. Additionally, 4,4'-Biphenyldiboronic acid has shown promise in biomedical applications, particularly in drug delivery systems due to its biocompatibility and ability to form reversible bonds with biomolecules. This compound stands out in its category, offering unique advantages for innovative research and development projects.

Synonyms
[4-(4-boronophenyl)phenyl]boronic acid
CAS Number
4151-80-8
Purity
≥ 95% (Assay by titration)
Molecular Formula
C12H12B2O4
Molecular Weight
241.84
MDL Number
MFCD00151795
PubChem ID
2734608
Melting Point
300 °C (dec.)
Appearance
White to green to brown crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
[4-(4-boronophenyl)phenyl]boronic acid
CAS Number
4151-80-8
Purity
≥ 95% (Assay by titration)
Molecular Formula
C12H12B2O4
Molecular Weight
241.84
MDL Number
MFCD00151795
PubChem ID
2734608
Melting Point
300 °C (dec.)
Appearance
White to green to brown crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4,4'-Biphenyldiboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Materials Science: It is employed in the creation of advanced materials, such as organic light-emitting diodes (OLEDs) and conductive polymers, enhancing their performance and stability.
  • Chemical Sensors: The compound is used in the development of chemical sensors, particularly for detecting biomolecules, which is vital in medical diagnostics and environmental monitoring.
  • Cross-Coupling Reactions: It plays a significant role in cross-coupling reactions, such as Suzuki-Miyaura coupling, allowing for the formation of carbon-carbon bonds in a highly efficient manner.
  • Drug Development: In medicinal chemistry, it aids in the design of boron-containing compounds that can target specific biological pathways, offering potential advantages in drug efficacy and selectivity.

Citations