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Catalog Number:
40297
CAS Number:
78495-63-3
2-Fluoro-6-methoxyphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2-Fluoro-6-methoxybenzeneboronic acid
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Product Information

2-Fluoro-6-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. 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 appreciate its role in the development of pharmaceuticals, agrochemicals, and advanced materials. The unique fluorine and methoxy substituents enhance its reactivity and selectivity, allowing for the efficient synthesis of complex organic molecules.

In addition to its applications in synthetic chemistry, 2-Fluoro-6-methoxyphenylboronic acid is also valuable in the field of sensor technology, where it can be employed in the detection of biomolecules. Its favorable properties, such as solubility in various organic solvents and stability under different conditions, make it an attractive choice for researchers looking to streamline their synthesis processes. With its broad range of applications and unique features, this compound stands out as a crucial tool in modern chemical research and development.

Synonyms
2-Fluoro-6-methoxybenzeneboronic acid
CAS Number
78495-63-3
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD02179483
PubChem ID
3294524
Melting Point
125 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Fluoro-6-methoxybenzeneboronic acid
CAS Number
78495-63-3
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD02179483
PubChem ID
3294524
Melting Point
125 °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-6-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 drugs targeting cancer and other diseases. Its unique structural features enhance the efficacy of drug candidates.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are crucial for forming carbon-carbon bonds in organic synthesis. This application is vital for creating complex molecules in the chemical industry.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, due to its ability to modify surface properties and enhance material performance.
  • Bioconjugation: In biochemistry, it facilitates the attachment of biomolecules to surfaces or other molecules, which is essential for creating biosensors and drug delivery systems.
  • Analytical Chemistry: It is utilized in the development of analytical methods for detecting and quantifying various substances, providing researchers with reliable tools for their studies.

Citations