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Catalog Number:
40374
CAS Number:
850991-69-4
5-Methoxypyridine-3-boronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
5-Methoxy-3-pyridylboronic acid
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Product Information

5-Methoxypyridine-3-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the development of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique methoxy group enhances solubility and reactivity, allowing for efficient coupling with various electrophiles. Researchers appreciate its role in synthesizing biologically active compounds, where it can contribute to the creation of novel drug candidates with improved efficacy.

In addition to its synthetic applications, 5-Methoxypyridine-3-boronic acid is also explored for its potential in material science, particularly in the development of functionalized polymers and sensors. Its favorable properties, such as stability and compatibility with various reaction conditions, make it a preferred choice for chemists looking to innovate in their respective fields. Whether you are involved in drug discovery or materials research, this compound offers significant advantages in efficiency and versatility.

Synonyms
5-Methoxy-3-pyridylboronic acid
CAS Number
850991-69-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C6H8BNO3
Molecular Weight
152.94
MDL Number
MFCD03425977
PubChem ID
2763087
Melting Point
230 - 270 °C
Appearance
White to almost white crystalline powder
Conditions
Store at ≤ -10 °C
General Information
Synonyms
5-Methoxy-3-pyridylboronic acid
CAS Number
850991-69-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C6H8BNO3
Molecular Weight
152.94
MDL Number
MFCD03425977
PubChem ID
2763087
Melting Point
230 - 270 °C
Appearance
White to almost white crystalline powder
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Methoxypyridine-3-boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It is used in the design of new drug candidates, especially for targeting specific biological pathways, enhancing the efficacy of treatments in areas like cancer and infectious diseases.
  • Material Science: The compound plays a crucial role in the development of advanced materials, including polymers and nanomaterials, due to its unique boronic acid functionality.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Cross-Coupling Reactions: This chemical is integral in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds in organic chemistry.

Citations