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Catalog Number:
40255
CAS Number:
609807-25-2
3-Fluoro-5-methoxyphenylboronic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
3-Fluoro-5-methoxybenzeneboronic acid
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Product Information

3-Fluoro-5-methoxyphenylboronic acid is a versatile compound that plays a crucial role in various chemical synthesis processes, particularly in the field of medicinal chemistry and organic synthesis. 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. Researchers and industry professionals utilize this compound for the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique fluorine and methoxy substituents enhance its reactivity and selectivity, allowing for the efficient construction of complex molecular architectures.

In addition to its synthetic applications, 3-Fluoro-5-methoxyphenylboronic acid is also valuable in the development of sensors and diagnostic tools due to its ability to selectively bind to specific biomolecules. This characteristic opens up possibilities for innovative applications in biosensing and targeted drug delivery systems. With its favorable properties and diverse applications, this compound stands out as a key player in modern chemical research and development.

Synonyms
3-Fluoro-5-methoxybenzeneboronic acid
CAS Number
609807-25-2
Purity
≥ 97% (HPLC)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD07363780
PubChem ID
2763243
Melting Point
172 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Fluoro-5-methoxybenzeneboronic acid
CAS Number
609807-25-2
Purity
≥ 97% (HPLC)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD07363780
PubChem ID
2763243
Melting Point
172 °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

3-Fluoro-5-methoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is crucial in synthesizing various pharmaceuticals, particularly in the development of anti-cancer agents. Its boronic acid functionality allows for the formation of stable complexes with diols, enhancing drug efficacy.
  • Organic Synthesis: It serves as a versatile building block in organic synthesis, facilitating the creation of complex molecules. Researchers often use it in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds.
  • Material Science: The compound is employed in the development of advanced materials, including polymers and nanomaterials. Its unique properties contribute to improved material performance in various applications, such as electronics and coatings.
  • Bioconjugation: It is used in bioconjugation techniques, where it helps in attaching biomolecules to surfaces or other molecules. This application is particularly valuable in creating targeted drug delivery systems and diagnostic tools.
  • Analytical Chemistry: The compound plays a role in analytical methods, such as chromatography and mass spectrometry. Its ability to form complexes enhances the detection and quantification of various analytes, making it a useful tool in laboratories.

Citations