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Catalog Number:
31086
CAS Number:
5122-94-1
4-Biphenylboronic acid(contains varying amounts of anhydride)
Purity:
≥ 99% (HPLC)
Synonym(s):
Biphenyl-4-boronic acid(Contains varying amounts of anhydride), 4-Phenylphenylboronic acid(contains varying amounts of anhydride)
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$18.53 /5G
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Product Information

4-Biphenylboronic acid is a versatile compound widely utilized in organic synthesis and materials science. Known for its ability to form stable complexes with various substrates, this boronic acid derivative is particularly valuable in Suzuki coupling reactions, which are essential for the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its unique structure allows for effective participation in cross-coupling reactions, making it a preferred choice for researchers in pharmaceuticals and agrochemicals looking to develop new compounds with enhanced properties.

Additionally, 4-Biphenylboronic acid is recognized for its role in sensor technology, where it can be employed in the detection of biomolecules and environmental pollutants. Its ability to interact selectively with diols makes it suitable for applications in biosensors and chemical sensors, providing a reliable method for monitoring various analytes. With its broad range of applications and effectiveness in facilitating complex reactions, 4-Biphenylboronic acid stands out as a crucial reagent for both academic research and industrial applications.

Synonyms
Biphenyl-4-boronic acid(Contains varying amounts of anhydride), 4-Phenylphenylboronic acid(contains varying amounts of anhydride)
CAS Number
5122-94-1
Purity
≥ 99% (HPLC)
Molecular Formula
C12H11BO2
Molecular Weight
198.03
MDL Number
MFCD00093311
PubChem ID
151253
Melting Point
232 - 245 ?C
Appearance
Off-white solid
Conditions
Store at RT
General Information
Synonyms
Biphenyl-4-boronic acid(Contains varying amounts of anhydride), 4-Phenylphenylboronic acid(contains varying amounts of anhydride)
CAS Number
5122-94-1
Purity
≥ 99% (HPLC)
Molecular Formula
C12H11BO2
Molecular Weight
198.03
MDL Number
MFCD00093311
PubChem ID
151253
Melting Point
232 - 245 ?C
Appearance
Off-white solid
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Biphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in the Suzuki-Miyaura cross-coupling reaction, enabling the formation of carbon-carbon bonds, which is essential for creating complex organic molecules.
  • Pharmaceutical Development: It is used in the synthesis of various pharmaceuticals, particularly in the development of antitumor agents and other therapeutic compounds, enhancing drug efficacy and specificity.
  • Material Science: The compound plays a role in the development of advanced materials, such as polymers and nanomaterials, due to its ability to form stable complexes with various substrates.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, which is crucial in diagnostics and research.
  • Environmental Applications: 4-Biphenylboronic acid is explored for use in sensors that detect environmental pollutants, providing a means to monitor and mitigate contamination effectively.

Citations