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Catalog Number:
31427
CAS Number:
352303-67-4
2-Fluoro-3-methoxyphenylboronic acid
Purity:
≥ 99.9% (HPLC)
Synonym(s):
2-Fluoro-3-methoxybenzeneboronic acid
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Product Information

2-Fluoro-3-methoxyphenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its unique ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the development of complex organic molecules. Its fluorine and methoxy substituents enhance its reactivity and selectivity, allowing for the efficient formation of carbon-carbon bonds. Researchers and industry professionals can leverage this compound in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

The practical applications of 2-Fluoro-3-methoxyphenylboronic acid extend to the development of novel drug candidates and functional materials. Its compatibility with various reaction conditions and substrates makes it a preferred choice for chemists aiming to streamline their synthetic pathways. Additionally, its unique properties can lead to improved yields and reduced reaction times compared to other boronic acids, providing significant advantages in both research and industrial settings.

Synonyms
2-Fluoro-3-methoxybenzeneboronic acid
CAS Number
352303-67-4
Purity
≥ 99.9% (HPLC)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD02094728
PubChem ID
4985744
Appearance
White to off-white powder
Conditions
Store at RT
General Information
Synonyms
2-Fluoro-3-methoxybenzeneboronic acid
CAS Number
352303-67-4
Purity
≥ 99.9% (HPLC)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD02094728
PubChem ID
4985744
Appearance
White to off-white 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-3-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 properties enhance the efficacy of drug candidates.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are essential for creating complex organic molecules. This application is crucial in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, due to its ability to form stable bonds with various substrates, enhancing material properties.
  • Bioconjugation: It plays a significant role in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other molecules, which is vital in diagnostics and therapeutic applications.
  • Research in Catalysis: This boronic acid is utilized in catalytic processes, improving reaction efficiencies and selectivities in synthetic chemistry, making it a valuable tool for researchers in the field.

Citations