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Catalog Number:
29071
CAS Number:
1692-15-5
4-Pyridinylboronic acid
Purity:
≥ 97% (GC)
Synonym(s):
Pyridine-4-boronic acid, 4-Pyridylboronic acid
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$18.53 /5G
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Product Information

4-Pyridylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a pyridine ring, which enhances its reactivity and makes it an essential building block for the development of various pharmaceuticals and agrochemicals. Its unique ability to form reversible covalent bonds with diols allows for applications in the design of sensors and drug delivery systems, making it invaluable in both research and industrial settings.

In addition to its role in cross-coupling reactions, 4-Pyridylboronic acid is also employed in the synthesis of complex organic molecules, including biologically active compounds. Researchers appreciate its effectiveness in Suzuki-Miyaura coupling reactions, which are crucial for constructing carbon-carbon bonds in the synthesis of advanced materials and pharmaceuticals. The compound's stability and ease of handling further enhance its appeal, making it a preferred choice for professionals seeking reliable reagents in their chemical processes.

Synonyms
Pyridine-4-boronic acid, 4-Pyridylboronic acid
CAS Number
1692-15-5
Purity
≥ 97% (GC)
Molecular Formula
C5H6BNO2
Molecular Weight
122.92
MDL Number
MFCD01074545
PubChem ID
2734379
Appearance
White to off-white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Pyridine-4-boronic acid, 4-Pyridylboronic acid
CAS Number
1692-15-5
Purity
≥ 97% (GC)
Molecular Formula
C5H6BNO2
Molecular Weight
122.92
MDL Number
MFCD01074545
PubChem ID
2734379
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-Pyridylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: It serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This is particularly valuable in the development of pharmaceuticals and agrochemicals.
  • Bioconjugation: The compound is used to attach biomolecules, such as proteins and nucleic acids, to surfaces or other molecules, which is essential in creating biosensors and drug delivery systems.
  • Fluorescent Probes: It can be utilized to develop fluorescent probes for detecting specific biomolecules, aiding in medical diagnostics and research applications.
  • Material Science: The compound is incorporated into polymer matrices to enhance material properties, such as conductivity and mechanical strength, which is beneficial in electronics and nanotechnology.
  • Environmental Applications: It is used in the detection and removal of pollutants, particularly in water treatment processes, due to its ability to form stable complexes with various contaminants.

Citations