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Catalog Number:
28497
CAS Number:
126747-14-6
4-Cyanophenylboronic acid
Purity:
≥ 99% (Assay)
Documents
$18.53 /1G
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Product Information

4-Cyanophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique properties allow for the selective functionalization of aromatic compounds, facilitating the synthesis of complex molecules. Researchers have leveraged 4-Cyanophenylboronic acid in Suzuki-Miyaura cross-coupling reactions, which are pivotal in creating biaryl compounds, a class of compounds with significant applications in drug discovery and materials science.

In addition to its role in synthetic chemistry, 4-Cyanophenylboronic acid has shown promise in the development of sensors and diagnostic tools due to its ability to interact with specific biomolecules. Its application in the preparation of fluorescent probes highlights its potential in biomedical research. With its robust reactivity and compatibility with various substrates, this compound stands out as a valuable asset for researchers and industry professionals seeking efficient pathways in chemical synthesis and analysis.

CAS Number
126747-14-6
Purity
≥ 99% (Assay)
Molecular Formula
C7H6BNO2
Molecular Weight
146.94
MDL Number
MFCD01318968
PubChem ID
2734326
Appearance
White to off-white powder
Conditions
Store at 0-8°C
General Information
CAS Number
126747-14-6
Purity
≥ 99% (Assay)
Molecular Formula
C7H6BNO2
Molecular Weight
146.94
MDL Number
MFCD01318968
PubChem ID
2734326
Appearance
White to off-white 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

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

  • Organic Synthesis: This compound serves as a key reagent in the Suzuki coupling reaction, facilitating the formation of carbon-carbon bonds, which is essential for creating complex organic molecules.
  • Pharmaceutical Development: It plays a crucial role in drug discovery, particularly in the design of boron-containing compounds that can enhance the efficacy of therapeutic agents.
  • Materials Science: Used in the development of advanced materials, it contributes to the synthesis of polymers and nanomaterials with tailored properties for electronics and photonics.
  • Bioconjugation: The compound is employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is vital in diagnostics and therapeutics.
  • Sensor Technology: It is utilized in the creation of chemical sensors, particularly for detecting specific ions or small molecules, enhancing the sensitivity and selectivity of analytical devices.

Citations