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Catalog Number:
40257
CAS Number:
179899-07-1
4-Fluoro-2-methoxyphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
4-Fluoro-2-methoxybenzeneboronic acid
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Product Information

4-Fluoro-2-methoxyphenylboronic acid is a versatile compound widely utilized 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 formation of complex organic molecules. Its unique fluorine and methoxy substituents enhance its reactivity and selectivity, allowing researchers to develop targeted pharmaceuticals and agrochemicals more effectively.

In addition to its synthetic applications, 4-Fluoro-2-methoxyphenylboronic acid is also valuable in the development of sensors and materials science, where its boron functionality can facilitate the formation of novel polymeric structures. The compound's stability and compatibility with various reaction conditions make it an ideal choice for both academic research and industrial applications. With its broad range of uses, this compound stands out as a crucial tool for chemists aiming to innovate in drug discovery and material development.

Synonyms
4-Fluoro-2-methoxybenzeneboronic acid
CAS Number
179899-07-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD03788423
PubChem ID
2782672
Melting Point
136 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Fluoro-2-methoxybenzeneboronic acid
CAS Number
179899-07-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD03788423
PubChem ID
2782672
Melting Point
136 °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

4-Fluoro-2-methoxyphenylboronic 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 the development of anti-cancer agents. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are essential for constructing complex organic molecules. This application is particularly valuable in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the creation of functionalized materials, such as polymers and nanomaterials, which have applications in electronics and sensors due to their unique electronic properties.
  • Bioconjugation: It plays a significant role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, which is crucial in diagnostics and therapeutic applications.
  • Research in Chemical Biology: The compound is utilized in studies aimed at understanding biological processes, particularly in the development of targeted therapies that can selectively interact with specific biological targets.

Citations