Boronic acid, specifically 3-(hydroxymethyl)-2-thienyl boronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a thienyl ring. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and alcohols, and possessing a moderate melting point. The thienyl moiety contributes to its aromatic character, which can influence its reactivity and interactions in various chemical environments. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis, particularly in the formation of boronate esters. Additionally, they play a significant role in medicinal chemistry and materials science due to their unique reactivity and ability to participate in cross-coupling reactions. The hydroxymethyl group enhances its solubility and reactivity, making it a useful building block in the synthesis of more complex organic molecules. Overall, this compound is significant in both academic research and industrial applications.

Boronic acid,[3-(hydroxymethyl)-2-thienyl]- (9CI)

222840-73-5: Boronic acid, specifically 3-(hydroxymethyl)-2-thienyl boronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a thienyl ring. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and alcohols, and possessing a moderate melting point. The thienyl moiety contributes to its aromatic character, which can influence its reactivity and interactions in various chemical environments. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis, particularly in the formation of boronate esters. Additionally, they play a significant role in medicinal chemistry and materials science due to their unique reactivity and ability to participate in cross-coupling reactions. The hydroxymethyl group enhances its solubility and reactivity, making it a useful building block in the synthesis of more complex organic molecules. Overall, this compound is significant in both academic research and industrial applications.

CAS 222840-73-5

Boronic acid,[3-(hydroxymethyl)-2-thienyl]- (9CI)

3-HYDROXYMETHYLTHIOPHENE-2-BORONIC ACID

Ref: IN-DA006Z1T