CAS 192376-68-4: 3-Fluoro-4-propoxyphenylboronic acid

Description: 3-Fluoro-4-propoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a fluorine atom and a propoxy group attached to a phenyl ring, which can influence its reactivity and solubility. The presence of the fluorine atom may enhance the compound's electronic properties, potentially affecting its interaction with biological targets. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the propoxy group can enhance the lipophilicity of the molecule, potentially improving its bioavailability in pharmaceutical applications. Overall, 3-Fluoro-4-propoxyphenylboronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry, particularly in the development of new therapeutic agents and materials.

Formula: C₉H₁₂BFO₃

InChI: InChI=1/C9H12BFO3/c1-2-5-14-9-4-3-7(10(12)13)6-8(9)11/h3-4,6,12-13H,2,5H2,1H3

Synonyms:

• 3-Fluor-4-Propoxyphenylboronic Acid
• 3-Fluoro-4-propoxyphenylboroni

Boronic acid, B-(3-fluoro-4-propoxyphenyl)-

CAS: 192376-68-4

• Formula: C₉H₁₂BFO₃
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 197.9992

3-Fluoro-4-propoxybenzeneboronic acid

CAS: 192376-68-4

• Formula: C₉H₁₂BFO₃
• Purity: By hplc: 99.3% by area (Typical Value in Batch COA)
• Color and Shape: off-white to beige powder
• Molecular weight: 198.00g/mol

(3-Fluoro-4-propoxyphenyl)boronic acid

CAS: 192376-68-4

• Purity: 95.0%
• Molecular weight: 198.0

3-Fluoro-4-propoxyphenylboronic acid

CAS: 192376-68-4

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• Formula: C₉H₁₂BFO₃
• Purity: Min. 95%
• Molecular weight: 198 g/mol