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Catalog Number:
17489
CAS Number:
372963-48-9
Acide 4-méthylpyridin-2-yl boronique
Purity:
≥ 95 % (RMN)
Synonym(s):
Acide 4-picoline-2-boronique, Acide 4-méthylpyridine-2-boronique
Documents
$65.40 /100 mg
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Product Information

4-Methylpyridin-2-yl boronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with various substrates, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure allows for selective functionalization, which is particularly beneficial in the development of pharmaceuticals and agrochemicals. Researchers appreciate its effectiveness in the synthesis of complex molecules, including biologically active compounds, due to its compatibility with a wide range of reaction conditions.

In addition to its applications in synthetic organic chemistry, 4-Methylpyridin-2-yl boronic acid has shown promise in the field of materials science, particularly in the development of sensors and catalysts. Its ability to interact with different functional groups enhances its utility in creating innovative materials with tailored properties. This compound stands out for its ease of use and the efficiency it brings to various chemical processes, making it a valuable addition to any laboratory focused on advanced chemical research and development.

Synonyms
Acide 4-picoline-2-boronique, Acide 4-méthylpyridine-2-boronique
CAS Number
372963-48-9
Purity
≥ 95 % (RMN)
Molecular Formula
C6H8BNO2
Molecular Weight
136.95
MDL Number
MFCD03093330
PubChem ID
2762744
Appearance
Solide blanc
Conditions
Conserver à 0-8°C
General Information
Synonyms
Acide 4-picoline-2-boronique, Acide 4-méthylpyridine-2-boronique
CAS Number
372963-48-9
Purity
≥ 95 % (RMN)
Molecular Formula
C6H8BNO2
Molecular Weight
136.95
MDL Number
MFCD03093330
PubChem ID
2762744
Appearance
Solide blanc
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Methylpyridin-2-yl boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Catalysis: It is employed as a catalyst in cross-coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds, enhancing efficiency in chemical manufacturing.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital in drug delivery systems and diagnostic applications.
  • Sensor Development: Its unique properties make it suitable for developing sensors that detect specific biomolecules, contributing to advancements in medical diagnostics and environmental monitoring.
  • Material Science: This boronic acid derivative plays a role in creating functional materials, such as hydrogels, which have applications in tissue engineering and controlled drug release.

Citations