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Catalog Number:
29071
CAS Number:
15 de mayo de 1692
Ácido 4-piridinilborónico
Purity:
≥ 97% (GC)
Synonym(s):
Ácido piridina-4-borónico, Ácido 4-piridilborónico
Documents
$18.53 /5G
Tamaño
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Product Information

Se utiliza en las reacciones de acoplamiento de Suzuki catalizadas por paladio.

Synonyms
Ácido piridina-4-borónico, Ácido 4-piridilborónico
CAS Number
15 de mayo de 1692
Purity
≥ 97% (GC)
Molecular Formula
C5H6BNO2
Molecular Weight
122.92
MDL Number
MFCD01074545
PubChem ID
2734379
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido piridina-4-borónico, Ácido 4-piridilborónico
CAS Number
15 de mayo de 1692
Purity
≥ 97% (GC)
Molecular Formula
C5H6BNO2
Molecular Weight
122.92
MDL Number
MFCD01074545
PubChem ID
2734379
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 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.

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