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

Catalog Number:
40249
CAS Number:
193353-34-3
2,5-Difluorophenylboronic acid
Purity:
≥ 98% (NMR)
Synonym(s):
2,5-Difluorobenzeneboronic acid
Documents
$70.91 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

2,5-Difluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to develop pharmaceuticals, agrochemicals, and advanced materials. Its fluorinated structure enhances lipophilicity and bioactivity, which can lead to improved efficacy in drug design and development.

In addition to its role in synthetic chemistry, 2,5-Difluorophenylboronic acid has shown promise in the development of sensors and catalysts, further expanding its application potential. The compound's compatibility with various reaction conditions and its ability to facilitate the formation of carbon-carbon bonds make it a valuable tool for chemists seeking to innovate in their respective fields. With its growing relevance in research and industry, 2,5-Difluorophenylboronic acid stands out as a key player in the advancement of modern chemical applications.

Synonyms
2,5-Difluorobenzeneboronic acid
CAS Number
193353-34-3
Purity
≥ 98% (NMR)
Molecular Formula
C6H5BF2O2
Molecular Weight
157.91
MDL Number
MFCD01863171
PubChem ID
2734335
Melting Point
244 - 247 °C
Appearance
White solid
Conditions
Store at RT
General Information
Synonyms
2,5-Difluorobenzeneboronic acid
CAS Number
193353-34-3
Purity
≥ 98% (NMR)
Molecular Formula
C6H5BF2O2
Molecular Weight
157.91
MDL Number
MFCD01863171
PubChem ID
2734335
Melting Point
244 - 247 °C
Appearance
White solid
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,5-Difluorophenylboronic 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 targeted cancer therapies.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic compounds, making it valuable for creating complex molecules.
  • Material Science: The compound is used in the production of advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of diagnostics and therapeutics.
  • Fluorescent Probes: 2,5-Difluorophenylboronic acid is utilized in the development of fluorescent probes for biological imaging, aiding in the visualization of cellular processes.

Citations