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Catalog Number:
40259
CAS Number:
871126-22-6
2-Fluoro-4-formylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2-Fluoro-4-formylbenzeneboronic acid
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Product Information

2-Fluoro-4-formylphenylboronic acid is a versatile compound with significant applications 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. Its unique fluorine substitution enhances its reactivity and selectivity, allowing for the development of novel pharmaceuticals and agrochemicals. Researchers in the field of drug discovery can leverage this compound to create targeted therapies, particularly in the development of compounds that require precise functionalization.

In addition to its synthetic utility, 2-Fluoro-4-formylphenylboronic acid is also valuable in materials science, where it can be used to modify surfaces or create advanced polymeric materials. Its ability to form stable complexes with various substrates opens up possibilities for innovative applications in sensors and catalysis. With its favorable properties and broad applicability, this compound stands out as a key reagent for professionals seeking to enhance their research and development efforts.

Synonyms
2-Fluoro-4-formylbenzeneboronic acid
CAS Number
871126-22-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H6BFO3
Molecular Weight
167.93
MDL Number
MFCD07367058
PubChem ID
16218045
Melting Point
178 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2-Fluoro-4-formylbenzeneboronic acid
CAS Number
871126-22-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H6BFO3
Molecular Weight
167.93
MDL Number
MFCD07367058
PubChem ID
16218045
Melting Point
178 °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

2-Fluoro-4-formylphenylboronic 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 unique structure allows for the modification of drug properties, enhancing efficacy.
  • Organic Synthesis: It plays a significant role in cross-coupling reactions, which are essential for creating complex organic molecules. This application is particularly valuable in the fields of materials science and organic electronics.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation techniques. This is crucial for creating targeted drug delivery systems and diagnostic tools.
  • Fluorescent Probes: The compound can be utilized in the development of fluorescent probes for biological imaging. Its ability to form stable complexes enhances the sensitivity and specificity of imaging techniques.
  • Environmental Chemistry: It is applied in the detection and removal of pollutants, particularly in water treatment processes. The compound’s reactivity allows for the capture of harmful substances, contributing to environmental protection efforts.

Citations