CAS 881998-70-5

B-(2-Ethyl-3-benzofuranyl)boronic acid

Description:

B-(2-Ethyl-3-benzofuranyl)boronic 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 and other nucleophiles. This compound features a benzofuran moiety, which contributes to its aromatic character and potential biological activity. The ethyl substituent enhances its solubility and reactivity. Boronic acids are often utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, making this compound valuable in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the benzofuran structure may impart unique electronic properties, influencing its reactivity and interaction with biological targets. The compound is typically handled with care due to the potential for moisture sensitivity, as boronic acids can hydrolyze in the presence of water. Overall, B-(2-Ethyl-3-benzofuranyl)boronic acid represents a versatile building block in synthetic organic chemistry, with applications in material science and medicinal chemistry.

Formula: C₁₀H₁₁BO₃

InChI: InChI=1S/C10H11BO3/c1-2-8-10(11(12)13)7-5-3-4-6-9(7)14-8/h3-6,12-13H,2H2,1H3

InChI key: InChIKey=XETMUIKOOLNLII-UHFFFAOYSA-N

SMILES: B(O)(O)C=1C=2C(OC1CC)=CC=CC2

Synonyms:

• B-(2-Ethyl-3-benzofuranyl)boronic acid
• Boronic acid, B-(2-ethyl-3-benzofuranyl)-
• (2-Ethyl-1-benzofuran-3-yl)boronic acid
• Boronic acid, (2-ethyl-3-benzofuranyl)-