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Catalog Number:
40281
CAS Number:
178305-99-2
2-Fluoro-4-biphenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
3-Fluoro-4-phenylbenzeneboronic acid
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Product Information

2-Fluoro-4-biphenylboronic acid is a versatile compound widely recognized for its utility in organic synthesis and medicinal chemistry. This boronic acid derivative features a fluorine atom that enhances its reactivity, making it an excellent candidate for Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its unique structure allows for the development of complex organic molecules, including pharmaceuticals and agrochemicals. Researchers appreciate its role in the synthesis of biologically active compounds, as it can facilitate the creation of novel drug candidates with improved efficacy and selectivity.

In addition to its synthetic applications, 2-Fluoro-4-biphenylboronic acid serves as a valuable tool in materials science, particularly in the development of organic electronic devices. Its ability to form stable complexes with various substrates opens avenues for innovative applications in sensor technology and catalysis. With its favorable properties and broad applicability, this compound stands out as a key ingredient for professionals seeking to advance research and development in chemistry and related fields.

Synonyms
3-Fluoro-4-phenylbenzeneboronic acid
CAS Number
178305-99-2
Purity
98 - 105% (Assay by titration)
Molecular Formula
C12H10BFO2
Molecular Weight
216.02
MDL Number
MFCD01075707
PubChem ID
2774698
Melting Point
248 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Fluoro-4-phenylbenzeneboronic acid
CAS Number
178305-99-2
Purity
98 - 105% (Assay by titration)
Molecular Formula
C12H10BFO2
Molecular Weight
216.02
MDL Number
MFCD01075707
PubChem ID
2774698
Melting Point
248 °C (Lit.)
Appearance
White 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

2-Fluoro-4-biphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently. Its unique structure enhances selectivity and yields in the formation of biaryl compounds.
  • Pharmaceutical Development: It plays a crucial role in the development of new pharmaceuticals, particularly in creating compounds that target specific biological pathways. Its ability to form stable complexes with various substrates makes it valuable in drug design.
  • Material Science: This chemical is used in the synthesis of advanced materials, including polymers and nanomaterials. Its properties enable the development of materials with enhanced electrical and thermal conductivity, which are essential in electronics.
  • Bioconjugation: The compound is utilized in bioconjugation techniques, where it helps attach biomolecules to surfaces or other compounds. This application is vital in creating biosensors and targeted drug delivery systems.
  • Research in Catalysis: It is employed in catalytic processes to facilitate various chemical reactions. Its effectiveness in catalysis can lead to more sustainable practices by reducing the need for harsh reaction conditions.

Citations