CAS 820240-91-3

Boronic acid, (6-methylbenzo[b]thien-2-yl)-

Description:

Boronic acid, (6-methylbenzo[b]thien-2-yl)-, identified by CAS number 820240-91-3, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a substituted benzo[b]thienyl moiety. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid group, which can engage in hydrogen bonding. The thienyl ring contributes to its aromatic character, potentially influencing its reactivity and stability. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the methyl group at the 6-position of the benzo[b]thienyl structure may affect the electronic properties and steric hindrance, which can influence the compound's reactivity and interactions in chemical reactions. Overall, this compound is of interest in the development of pharmaceuticals and materials science due to its unique structural features and functional properties.

Formula: C₉H₉BO₂S

Synonyms:

• (6-Methylbenzo[b]thiophen-2-yl)boronic acid
• Boronic acid, B-(6-methylbenzo[b]thien-2-yl)-
• 6-METHYLBENZO[B]THIENE-2-BORONIC ACID
• 6-METHYLBENZO[B]THIEN-2-YL BORONIC ACID

(6-Methylbenzo[b]thiophen-2-yl)boronic acid

CAS: 820240-91-3

Formula: C₉H₉BO₂S

Molecular weight: 192.0426

Ref: IN-DA005D7F

(6-Methyl-1-benzothiophen-2-yl)boronic acid

CAS: 820240-91-3

Versatile small molecule scaffold

Formula: C₉H₉BO₂S

Purity: Min. 95%

Molecular weight: 192.05 g/mol

Ref: 3D-VHB24091