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Catalog Number:
40364
CAS Number:
162607-19-4
Dibenzofuran-1-boronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Dibenzo[b,d]furan-1-ylboronic acid, Dibenzofuran-1-ylboronic acid
Documents
$65.40 /1G
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Product Information

Dibenzofuran-1-boronic acid is a versatile compound widely recognized for its utility in organic synthesis and medicinal chemistry. This boronic acid derivative features a dibenzofuran core, which enhances its reactivity and compatibility with various coupling reactions, making it an essential building block in the development of pharmaceuticals and agrochemicals. Its unique structure allows for the formation of stable complexes with diols, facilitating applications in the synthesis of complex organic molecules. Researchers often utilize dibenzofuran-1-boronic acid in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing carbon-carbon bonds, thereby enabling the creation of diverse chemical entities.

Moreover, this compound's ability to act as a ligand in coordination chemistry opens avenues for its use in catalysis and material science. Its stability and functional versatility make it an attractive choice for researchers aiming to innovate in drug discovery and development. With its proven track record in enhancing reaction efficiency and selectivity, dibenzofuran-1-boronic acid stands out as a valuable asset in both academic and industrial settings.

Synonyms
Dibenzo[b,d]furan-1-ylboronic acid, Dibenzofuran-1-ylboronic acid
CAS Number
162607-19-4
Purity
≥ 98% (HPLC)
Molecular Formula
C12H9BO3
Molecular Weight
212.01
MDL Number
MFCD01318978
PubChem ID
17750867
Appearance
White to almost white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Dibenzo[b,d]furan-1-ylboronic acid, Dibenzofuran-1-ylboronic acid
CAS Number
162607-19-4
Purity
≥ 98% (HPLC)
Molecular Formula
C12H9BO3
Molecular Weight
212.01
MDL Number
MFCD01318978
PubChem ID
17750867
Appearance
White to almost 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

Dibenzofuran-1-boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Discovery: Its unique boronic acid functionality allows for the formation of reversible covalent bonds with biomolecules, making it valuable in the design of targeted drug candidates, especially in cancer therapy.
  • Material Science: Used in the development of advanced materials, it contributes to the creation of organic light-emitting diodes (OLEDs) and other electronic devices due to its excellent electronic properties.
  • Bioconjugation: The compound is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.
  • Environmental Chemistry: It plays a role in the study of environmental pollutants, aiding in the development of sensors and remediation strategies for detecting and removing harmful substances.

Citations