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Catalog Number:
31441
CAS Number:
768-35-4
3-Fluorophenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
3-Fluorobenzeneboronic acid, m-Fluorobenzeneboronic acid
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Product Information

3-Fluorophenylboronic acid is a versatile organoboron compound recognized for its unique reactivity and functional properties. This compound is particularly valued in organic synthesis and medicinal chemistry, where it serves as a crucial building block for the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with various substrates makes it an essential reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Researchers and industry professionals utilize 3-Fluorophenylboronic acid in the synthesis of biologically active compounds, including potential drug candidates, due to its favorable electronic properties and the presence of the fluorine atom, which can enhance the compound's bioactivity and selectivity.

Additionally, 3-Fluorophenylboronic acid is employed in the development of sensors and materials, where its boronic acid functionality allows for the detection of diols and sugars, making it useful in biochemical applications. Its unique characteristics, such as high stability and ease of handling, further contribute to its appeal in both laboratory and industrial settings. With its broad range of applications, 3-Fluorophenylboronic acid stands out as a valuable tool for researchers aiming to innovate in chemical synthesis and material science.

Synonyms
3-Fluorobenzeneboronic acid, m-Fluorobenzeneboronic acid
CAS Number
768-35-4
Purity
≥ 99% (HPLC)
Molecular Formula
C6H6BFO2
Molecular Weight
139.92
MDL Number
MFCD00236042
PubChem ID
2733986
Melting Point
214 - 218 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Fluorobenzeneboronic acid, m-Fluorobenzeneboronic acid
CAS Number
768-35-4
Purity
≥ 99% (HPLC)
Molecular Formula
C6H6BFO2
Molecular Weight
139.92
MDL Number
MFCD00236042
PubChem ID
2733986
Melting Point
214 - 218 ?C
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

3-Fluorophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound plays a crucial role in synthesizing pharmaceuticals, particularly in the development of targeted cancer therapies, where it helps in the design of boron-containing drugs that can effectively deliver therapeutic agents to cancer cells.
  • Organic Synthesis: It is commonly used as a building block in organic chemistry, facilitating the formation of complex molecules through Suzuki coupling reactions, which are essential in creating various organic compounds.
  • Material Science: This chemical is employed in the production of advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings, enhancing material properties like conductivity and durability.
  • Bioconjugation: In biochemistry, it is used for labeling biomolecules, allowing researchers to track and study proteins and other biological entities, which is vital for understanding cellular processes and disease mechanisms.
  • Environmental Chemistry: The compound is also utilized in the detection and analysis of environmental pollutants, helping in the development of sensors that can monitor water quality and detect harmful substances.

Citations