5-Ethylthiophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thiophene ring that is further substituted with an ethyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The thiophene moiety contributes to its aromatic character and may influence its electronic properties, enhancing its reactivity in cross-coupling reactions, particularly in Suzuki-Miyaura coupling. Additionally, the presence of the ethyl group can affect solubility and steric hindrance, which are important factors in its reactivity and interaction with other molecules. Overall, 5-ethylthiophenylboronic acid is valuable in the development of pharmaceuticals and materials science due to its unique structural features and reactivity profile.

5-ETHYLTHIOPHENYLBORONIC ACID

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Boronic acid, B-(5-ethyl-2-thienyl)-

5-Ethylthiophene-2-boronic acid

5-Ethylthiophene-2-boronic acid (ETBA) is a boronic acid that can reversibly bind to a wide range of organic compounds. It has been shown to have antioxidant properties and is being investigated as an additive for detergents, marine bacterium screening, and research. ETBA has been shown to inhibit the growth of bacteria by binding to the active site of enzymes such as 5-lipoxygenase in marine bacterium. This mechanism may be due to its ability to scavenge free radicals or chelate metal ions.

CAS 162607-16-1: 5-ETHYLTHIOPHENYLBORONIC ACID

Boronic acid, B-(5-ethyl-2-thienyl)-

Ref: IN-DA001T94

5-Ethylthiophene-2-boronic acid

Ref: 54-OR361223

5-Ethylthiophene-2-boronicacid

Ref: 3D-FE149402