Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40220
CAS Number:
843663-18-3
4-Cyano-3-fluorophenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Cyano-3-fluorobenzeneboronic acid
Documents
$36.65 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

4-Cyano-3-fluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its unique cyano and fluorine substituents enhance its reactivity and selectivity, allowing for the development of complex molecular architectures that are crucial in pharmaceutical research and development.

In addition to its applications in synthetic chemistry, 4-Cyano-3-fluorophenylboronic acid has shown potential in the development of novel materials and sensors due to its electronic properties. Researchers have leveraged its unique characteristics to create advanced materials for electronic applications, showcasing its versatility beyond traditional uses. This compound is particularly valuable for those in the pharmaceutical and materials science industries, offering a reliable option for innovative research and development projects.

Synonyms
4-Cyano-3-fluorobenzeneboronic acid
CAS Number
843663-18-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H5BFNO2
Molecular Weight
164.93
MDL Number
MFCD03411549
PubChem ID
2783130
Melting Point
> 300 °C
Appearance
White to off white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Cyano-3-fluorobenzeneboronic acid
CAS Number
843663-18-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H5BFNO2
Molecular Weight
164.93
MDL Number
MFCD03411549
PubChem ID
2783130
Melting Point
> 300 °C
Appearance
White to off white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Cyano-3-fluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-cancer agents. Its unique structure allows for targeted modifications that enhance drug efficacy.
  • Organic Synthesis: It plays a significant role in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for creating complex organic molecules used in agrochemicals and materials science.
  • Fluorescent Probes: The compound can be used to develop fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes and disease mechanisms in real-time.
  • Sensor Technology: Its properties make it suitable for creating sensors that detect specific biomolecules, which is crucial in diagnostics and environmental monitoring.
  • Material Science: It is employed in the development of advanced materials, including polymers and nanomaterials, that exhibit enhanced electrical and thermal properties, beneficial for electronics and energy applications.

Citations