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Catalog Number:
28918
CAS Number:
854373-97-0
2-Ethoxypyridine-3-boronic acid
Purity:
≥ 98% (HPLC)
Documents
$36.65 /1G
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Product Information

2-Ethoxypyridine-3-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 pharmaceuticals and agrochemicals. Its unique structure enhances its reactivity and selectivity, making it an ideal choice for researchers looking to create complex molecular architectures. Additionally, the presence of the ethoxy group contributes to its solubility in various organic solvents, facilitating easier handling and application in laboratory settings.

In the pharmaceutical industry, 2-Ethoxypyridine-3-boronic acid has shown promise in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its ability to participate in diverse coupling reactions allows for the efficient construction of intricate molecular frameworks, which is crucial in drug discovery and development. With its favorable properties and practical applications, this compound stands out as a valuable tool for chemists and researchers aiming to innovate and streamline their synthetic processes.

CAS Number
854373-97-0
Purity
≥ 98% (HPLC)
Molecular Formula
C7H10BNO3
Molecular Weight
166.97
MDL Number
MFCD06201036
PubChem ID
11309733
Melting Point
104 °C
Appearance
White or off-white crystalline powder
Conditions
Store at 0-8°C
General Information
CAS Number
854373-97-0
Purity
≥ 98% (HPLC)
Molecular Formula
C7H10BNO3
Molecular Weight
166.97
MDL Number
MFCD06201036
PubChem ID
11309733
Melting Point
104 °C
Appearance
White or off-white crystalline powder
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-Ethoxypyridine-3-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in developing targeted therapies for cancer and other diseases.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is vital for creating complex organic molecules used in agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties like strength and conductivity.
  • Bioconjugation: It plays a role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Analytical Chemistry: The compound is utilized in the preparation of sensors and probes for detecting specific biomolecules, aiding in environmental monitoring and medical diagnostics.

Citations