CAS 681292-77-3

4-Chloro-3-propoxyphenylboronic acid

Description:

4-Chloro-3-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 chlorinated aromatic ring, which can influence its reactivity and solubility. The propoxy group enhances its lipophilicity, potentially improving its bioavailability in pharmaceutical contexts. This compound is typically used in the development of boron-containing drugs and as a reagent in Suzuki coupling reactions, which are vital for constructing complex organic molecules. Its boronic acid moiety allows for the formation of stable complexes with carbohydrates, making it relevant in biochemical applications. Safety data sheets should be consulted for handling and storage guidelines, as boronic acids can exhibit toxicity and require proper safety measures during use. Overall, 4-Chloro-3-propoxyphenylboronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

Formula: C₉H₁₂BClO₃

Synonyms:

• Boronic acid, B-(4-chloro-3-propoxyphenyl)-
• 4-Chloro-3-propoxyphenylboronic acid

4-Chloro-3-propoxyphenylboronic acid

CAS: 681292-77-3

Formula: C₉H₁₂BClO₃

Molecular weight: 214.4538

Ref: IN-DA005MNY

4-Chloro-3-propoxyphenylboronic acid

CAS: 681292-77-3

4-Chloro-3-propoxyphenylboronic acid

Purity: ≥95%

Molecular weight: 214.45g/mol

Ref: 54-OR360553