B-(3-Bromo-2-thienyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a brominated thiophene ring. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. The bromine substituent on the thiophene ring enhances its reactivity, making it useful in various organic synthesis applications, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. The boronic acid group allows for the formation of stable complexes with diols, which is significant in the development of sensors and in medicinal chemistry for drug design. Additionally, this compound may exhibit interesting electronic properties due to the conjugated system of the thiophene ring, making it a candidate for applications in organic electronics and materials science. Overall, B-(3-Bromo-2-thienyl)boronic acid is a versatile building block in synthetic organic chemistry.

B-(3-Bromo-2-thienyl)boronic acid

162607-26-3: (3-Bromo-2-Thienyl)-Boronic Acid, (3-Bromo-2-thiophenyl)boronic acid, (3-Bromothiophen-2-Yl)Boronic Acid, 3-BroMo-2-thiopheneboronic acid, 3-Bromothien-2-Ylboronic Acid, B-(3-Bromo-2-thienyl)boronic acid, Boronic acid, (3-bromo-2-thienyl)-, Boronic acid, B-(3-bromo-2-thienyl)-, Rarechem Ah Pb 0068

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CAS 162607-26-3: B-(3-Bromo-2-thienyl)boronic acid

3-Bromothiophene-2-boronic acid

Ref: 3D-FB33261

(3-Bromothiophen-2-yl)boronic acid

Ref: 10-F225804

3-BROMOTHIOPHENE-2-BORONIC ACID

Ref: IN-DA00ACT2