Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
28849
CAS Number:
1692-25-7
Pyridine-3-boronic acid
Purity:
≥ 99% (Titration)
Documents
$18.53 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

Pyridine-3-boronic acid is a versatile organoboron compound that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of biaryl compounds, which are significant in the development of pharmaceuticals and agrochemicals. Its unique boronic acid functionality allows for the selective formation of carbon-carbon bonds, enabling researchers to create complex molecular architectures with precision.

In addition to its synthetic applications, Pyridine-3-boronic acid is also utilized in the development of sensors and catalysts, showcasing its adaptability across various fields. Its stability and ease of handling further enhance its appeal for laboratory use, making it a preferred choice for chemists seeking reliable reagents. With its broad range of applications, Pyridine-3-boronic acid stands out as a valuable tool for researchers and industry professionals aiming to innovate in chemical synthesis and material science.

CAS Number
1692-25-7
Purity
≥ 99% (Titration)
Molecular Formula
C5H6BNO2
Molecular Weight
122.92
MDL Number
MFCD00674177
PubChem ID
2734378
Appearance
White to off-white powder.
Conditions
Store at 0-8 °C
General Information
CAS Number
1692-25-7
Purity
≥ 99% (Titration)
Molecular Formula
C5H6BNO2
Molecular Weight
122.92
MDL Number
MFCD00674177
PubChem ID
2734378
Appearance
White to off-white powder.
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Pyridine-3-boronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a crucial building block in the synthesis of various pharmaceuticals and agrochemicals, enabling the creation of complex molecules with enhanced biological activity.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds, making it valuable in developing new materials and fine chemicals.
  • Bioconjugation: Pyridine-3-boronic acid can be employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is beneficial in drug delivery and diagnostic applications.
  • Fluorescent Probes: This compound is utilized in the design of fluorescent probes for detecting specific biomolecules, aiding in biological research and medical diagnostics.
  • Environmental Applications: It can be used in the development of sensors for detecting pollutants, contributing to environmental monitoring and protection efforts.

Citations