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Catalog Number:
17516
CAS Number:
372963-50-3
Ácido 6-metilpiridina-2-borónico
Purity:
≥ 97 % (HPLC)
Synonym(s):
Ácido 6-picolina-2-borónico
Documents
$125.80 /100 mg
Tamaño
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Product Information

6-Methylpyridine-2-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the development of complex organic molecules. Its unique structure, featuring a methyl group on the pyridine ring, enhances its reactivity and selectivity, making it an ideal candidate for synthesizing pharmaceuticals and agrochemicals. Researchers and industry professionals appreciate its effectiveness in creating diverse compounds, including biologically active molecules and functional materials.

In addition to its synthetic applications, 6-Methylpyridine-2-boronic acid serves as a valuable building block in the development of sensors and catalysts. Its ability to form stable complexes with various substrates allows for innovative applications in material science and nanotechnology. The compound's compatibility with a range of reaction conditions further expands its utility, making it a preferred choice for chemists seeking reliable and efficient solutions in their research and development projects.

Synonyms
Ácido 6-picolina-2-borónico
CAS Number
372963-50-3
Purity
≥ 97 % (HPLC)
Molecular Formula
C6H8BNO2
Molecular Weight
136.95
MDL Number
MFCD03093331
PubChem ID
2762742
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 6-picolina-2-borónico
CAS Number
372963-50-3
Purity
≥ 97 % (HPLC)
Molecular Formula
C6H8BNO2
Molecular Weight
136.95
MDL Number
MFCD03093331
PubChem ID
2762742
Appearance
Sólido blanco
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

6-Methylpyridine-2-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.
  • Cross-Coupling Reactions: It is extensively used in Suzuki-Miyaura coupling reactions, which are vital for forming carbon-carbon bonds in complex organic compounds.
  • Material Science: The compound is applied in creating advanced materials, including polymers and nanomaterials, enhancing their properties through boron chemistry.
  • Bioconjugation: It plays a role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is important in drug delivery systems.
  • Analytical Chemistry: This boronic acid derivative is used in sensor development for detecting sugars and other biomolecules, providing a sensitive method for various analytical applications.

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