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Catalog Number:
31437
CAS Number:
87199-17-5
4-Formylphenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
4-Formylbenzeneboronic acid, p-Formylphenylboronic acid
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Product Information

4-Formylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a formyl group that enhances its reactivity, making it an excellent candidate for various coupling reactions, including Suzuki-Miyaura cross-coupling. Its ability to form stable complexes with diols and other Lewis bases allows for applications in sensor technology and the development of novel materials. Researchers appreciate its role in the synthesis of biologically active compounds, particularly in the pharmaceutical industry, where it can be employed to create targeted drug delivery systems and advanced therapeutic agents.

Additionally, 4-Formylphenylboronic acid stands out for its compatibility with a range of functional groups, facilitating the construction of complex molecular architectures. Its unique properties make it a valuable tool for chemists looking to innovate in areas such as polymer chemistry and catalysis. With its proven efficacy and broad applicability, this compound is an essential addition to any researcher's toolkit, driving advancements in both academic and industrial settings.

Synonyms
4-Formylbenzeneboronic acid, p-Formylphenylboronic acid
CAS Number
87199-17-5
Purity
≥ 99% (HPLC)
Molecular Formula
C7H7BO3
Molecular Weight
149.94
MDL Number
MFCD00151823
PubChem ID
591073
Melting Point
240 - 250 ?C
Appearance
Pale yellow to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Formylbenzeneboronic acid, p-Formylphenylboronic acid
CAS Number
87199-17-5
Purity
≥ 99% (HPLC)
Molecular Formula
C7H7BO3
Molecular Weight
149.94
MDL Number
MFCD00151823
PubChem ID
591073
Melting Point
240 - 250 ?C
Appearance
Pale yellow to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Formylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its ability to form stable complexes with biomolecules makes it valuable in drug discovery, aiding in the design of targeted therapies.
  • Material Science: Used in the production of advanced materials, it contributes to the creation of polymers and composites with enhanced properties.
  • Bioconjugation: This chemical is effective in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other compounds, which is crucial in diagnostics and therapeutic applications.
  • Chemical Sensors: Its unique properties enable the development of sensitive chemical sensors for detecting environmental pollutants or biological markers.

Citations