Atomfair 5-Fluoro-2-methoxyphenylboronic acid C7H8BFO3

Description 5-Fluoro-2-methoxyphenylboronic acid (CAS No. 179897-94-0) is a high-purity boronic acid derivative with the molecular formula C7H8BFO3. This compound is a versatile building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl structures with high efficiency. The presence of both fluoro and methoxy substituents on the phenyl ring enhances its reactivity and selectivity in coupling reactions. Ideal for pharmaceutical, agrochemical, and materials science research, this boronic acid is supplied with rigorous quality control to ensure consistency in your experiments. Store in a cool, dry place, protected from moisture to maintain stability.

Description

5-Fluoro-2-methoxyphenylboronic acid (CAS No. 179897-94-0) is a high-purity boronic acid derivative with the molecular formula C₇H₈BFO₃. This compound is a versatile building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl structures with high efficiency. The presence of both fluoro and methoxy substituents on the phenyl ring enhances its reactivity and selectivity in coupling reactions. Ideal for pharmaceutical, agrochemical, and materials science research, this boronic acid is supplied with rigorous quality control to ensure consistency in your experiments. Store in a cool, dry place, protected from moisture to maintain stability.

CAS No: 179897-94-0
Molecular Formula: C7H8BFO3
Molecular Weight: 169.95
Exact Mass: 170.0550524
Monoisotopic Mass: 170.0550524
IUPAC Name: (5-fluoro-2-methoxyphenyl)boronic acid
SMILES: B(C1=C(C=CC(=C1)F)OC)(O)O
Synonyms: 5-Fluoro-2-methoxyphenylboronic acid, 179897-94-0, (5-fluoro-2-methoxyphenyl)boronic acid, DTXSID70382204, DTXCID00333229

Application

5-Fluoro-2-methoxyphenylboronic acid is widely used in pharmaceutical research for the synthesis of fluorinated drug candidates. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions to construct complex aromatic systems. The compound is also employed in the development of agrochemicals and functional materials due to its unique electronic properties.

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