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Catalog Number:
40345
CAS Number:
849062-00-6
3-Ethoxy-2,6-difluorophenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-Ethoxy-2,6-difluorobenzeneboronic acid
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Product Information

3-Ethoxy-2,6-difluorophenylboronic acid is a versatile compound widely utilized in pharmaceutical and chemical research. This boronic acid derivative is particularly valuable in the synthesis of biologically active molecules, serving as a key building block in the development of targeted therapies. Its unique structure, featuring both ethoxy and difluorophenyl groups, enhances its reactivity and selectivity in cross-coupling reactions, making it an essential reagent in medicinal chemistry. Researchers have leveraged its properties to create novel compounds with potential applications in treating various diseases, including cancer and infectious diseases.

In addition to its role in drug discovery, 3-Ethoxy-2,6-difluorophenylboronic acid is also employed in materials science for the development of advanced polymers and sensors. Its ability to form stable complexes with various substrates opens up possibilities for innovative applications in catalysis and environmental chemistry. With its unique features and broad applicability, this compound stands out as a crucial tool for researchers and industry professionals seeking to push the boundaries of chemical synthesis and material development.

Synonyms
3-Ethoxy-2,6-difluorobenzeneboronic acid
CAS Number
849062-00-6
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H9BF2O3
Molecular Weight
201.96
MDL Number
MFCD07369735
PubChem ID
16217893
Melting Point
97 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Ethoxy-2,6-difluorobenzeneboronic acid
CAS Number
849062-00-6
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H9BF2O3
Molecular Weight
201.96
MDL Number
MFCD07369735
PubChem ID
16217893
Melting Point
97 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Ethoxy-2,6-difluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is valuable in the synthesis of various pharmaceuticals, particularly in creating targeted therapies for cancer treatment, due to its ability to form stable complexes with biologically relevant molecules.
  • Organic Synthesis: It serves as a key reagent in Suzuki coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in the development of complex organic molecules.
  • Material Science: The compound is used in the fabrication of advanced materials, including polymers and nanomaterials, enhancing properties like conductivity and mechanical strength.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostic and therapeutic applications.
  • Research in Fluorinated Compounds: Its unique fluorine substituents make it a subject of interest in studies exploring the effects of fluorination on chemical reactivity and biological activity, providing insights into drug design.

Citations