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Catalog Number:
28917
CAS Number:
612845-44-0
Acide 6-éthoxy-3-pyridinylboronique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Acide 2-éthoxy-5-pyridineboronique
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Product Information

2-Ethoxy-5-pyridineboronic 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 synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure allows for the formation of stable complexes with various substrates, enhancing reaction efficiency and selectivity.

Researchers and industry professionals appreciate 2-Ethoxy-5-pyridineboronic acid for its solubility in common organic solvents, which facilitates its use in diverse reaction conditions. Its applications extend to the development of novel materials and the synthesis of biologically active compounds, showcasing its relevance in drug discovery and development. With its favorable reactivity profile and compatibility with various functional groups, this compound stands out as a valuable tool for chemists aiming to innovate and optimize synthetic pathways.

Synonyms
Acide 2-éthoxy-5-pyridineboronique
CAS Number
612845-44-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C7H10BNO3
Molecular Weight
166.97
MDL Number
MFCD06201032
PubChem ID
12012237
Melting Point
115-122 ?C
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide 2-éthoxy-5-pyridineboronique
CAS Number
612845-44-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C7H10BNO3
Molecular Weight
166.97
MDL Number
MFCD06201032
PubChem ID
12012237
Melting Point
115-122 ?C
Appearance
Poudre blanche à blanc cassé
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

2-Ethoxy-5-pyridineboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents. Its boronic acid functionality allows for selective interactions with biological targets.
  • Chemical Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential in forming carbon-carbon bonds. This is particularly valuable in creating complex organic molecules in the agrochemical and pharmaceutical industries.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, that require precise chemical modifications for enhanced properties, such as conductivity and strength.
  • Bioconjugation: Its ability to form stable complexes with biomolecules makes it useful in bioconjugation processes, aiding in the development of targeted drug delivery systems and diagnostic tools.
  • Research Applications: In academic and industrial research, it is utilized for studying reaction mechanisms and developing new synthetic methodologies, providing insights that can lead to more efficient chemical processes.

Citations