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Catalog Number:
28849
CAS Number:
25 de julio de 1692
Ácido piridina-3-borónico
Purity:
≥ 99% (titulación)
Documents
$18.53 /5G
Tamaño
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Product Information

Reactivo versátil en la reacción de acoplamiento cruzado de Suzuki-Miyaura para hacer
Formación de enlaces CC.

CAS Number
25 de julio de 1692
Purity
≥ 99% (titulación)
Molecular Formula
C5H6BNO2
Molecular Weight
122.92
MDL Number
MFCD00674177
PubChem ID
2734378
Appearance
Polvo de color blanco a blanquecino.
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
25 de julio de 1692
Purity
≥ 99% (titulación)
Molecular Formula
C5H6BNO2
Molecular Weight
122.92
MDL Number
MFCD00674177
PubChem ID
2734378
Appearance
Polvo de color blanco a blanquecino.
Conditions
Conservar entre 0 y 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.

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