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Catalog Number:
26691
CAS Number:
1100095-25-7
[3-(1H-Pyrazol-5-yl)phenyl]boronic acid
Purity:
≥ 97% (NMR)
Documents
$65.40 /100MG
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Product Information

[3-(1H-Pyrazol-5-yl)phenyl]boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for applications in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules. Researchers appreciate its role in the creation of biologically active compounds, particularly in the development of targeted therapies and novel drug candidates.

In addition to its synthetic utility, [3-(1H-Pyrazol-5-yl)phenyl]boronic acid has shown promise in the field of materials science, where it can be employed in the fabrication of advanced materials with tailored properties. Its compatibility with various substrates enhances its application potential in sensor technology and catalysis. With its broad range of applications and unique properties, this compound stands out as a valuable tool for researchers and industry professionals aiming to innovate and enhance their projects.

CAS Number
1100095-25-7
Purity
≥ 97% (NMR)
Molecular Formula
C9H9BN2O2
Molecular Weight
188.0
MDL Number
MFCD08059896
PubChem ID
25248075
Appearance
White powder
Conditions
Store at 0-8°C
General Information
CAS Number
1100095-25-7
Purity
≥ 97% (NMR)
Molecular Formula
C9H9BN2O2
Molecular Weight
188.0
MDL Number
MFCD08059896
PubChem ID
25248075
Appearance
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

[3-(1H-Pyrazol-5-yl)phenyl]boronic acid is widely utilized in research focused on:

  • Drug Development: This compound is instrumental in the synthesis of various pharmaceutical agents, particularly in developing targeted therapies for cancer, due to its ability to form stable complexes with biomolecules.
  • Chemical Sensing: It serves as a key component in creating sensors that detect specific analytes, enhancing the sensitivity and selectivity of chemical detection in environmental monitoring.
  • Organic Electronics: The compound is used in the fabrication of organic semiconductors, contributing to the development of more efficient electronic devices, such as organic light-emitting diodes (OLEDs).
  • Cross-Coupling Reactions: It plays a vital role in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis, allowing for the creation of complex molecular architectures.
  • Agricultural Chemistry: This boronic acid derivative is explored for its potential in developing herbicides and pesticides, offering a more targeted approach to pest management while minimizing environmental impact.

Citations