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Catalog Number:
28965
CAS Number:
163105-90-6
2-Methoxypyridine-3-boronic acid
Purity:
≥ 98% (HPLC)
Documents
$22.83 /1G
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Product Information

2-Methoxypyridine-3-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of biaryl compounds. Its unique structure, featuring a methoxy group, enhances its solubility and reactivity, allowing for efficient coupling with a variety of electrophiles. Researchers and industry professionals leverage this compound in the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

Additionally, 2-Methoxypyridine-3-boronic acid serves as a valuable reagent in the synthesis of complex organic molecules, contributing to the advancement of drug discovery and development. Its compatibility with various functional groups and ease of handling make it a preferred choice for chemists seeking reliable and effective solutions in their synthetic pathways. With its proven track record in enhancing reaction yields and facilitating the creation of diverse chemical entities, this compound stands out as a key player in modern organic chemistry.

CAS Number
163105-90-6
Purity
≥ 98% (HPLC)
Molecular Formula
C6H8BNO3·H2O
Molecular Weight
170.96
MDL Number
MFCD03411572
PubChem ID
2762709
Appearance
White to off-white solid
Conditions
Store at 0-8°C
General Information
CAS Number
163105-90-6
Purity
≥ 98% (HPLC)
Molecular Formula
C6H8BNO3·H2O
Molecular Weight
170.96
MDL Number
MFCD03411572
PubChem ID
2762709
Appearance
White to off-white solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Synthetic Chemistry: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Catalysis: It is employed as a ligand in palladium-catalyzed cross-coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis, enhancing reaction efficiency and selectivity.
  • Bioconjugation: The boronic acid functional group allows for selective binding to diols, making it useful in bioconjugation techniques for drug delivery systems and targeted therapies.
  • Material Science: It is used in the development of advanced materials, including sensors and polymers, due to its ability to form stable complexes with various substrates.
  • Analytical Chemistry: This compound can be utilized in the development of analytical methods for detecting and quantifying certain biomolecules, providing a reliable tool for researchers in biochemistry.

Citations