B-(4-Bromo-2-thienyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thienyl ring that is further substituted with a bromine atom. This compound typically exhibits properties such as moderate solubility in polar organic solvents and can participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis for forming carbon-carbon bonds. The presence of the bromine atom enhances its reactivity and allows for further functionalization. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in biological and chemical applications. The thienyl moiety contributes to the compound's electronic properties, potentially influencing its behavior in electronic materials or as a ligand in coordination chemistry. Overall, B-(4-Bromo-2-thienyl)boronic acid is a versatile compound with applications in synthetic organic chemistry, materials science, and medicinal chemistry.

B-(4-Bromo-2-thienyl)boronic acid

499769-92-5: 4-Bromo-2-thienylboronic acid, B-(4-Bromo-2-thienyl)boronic acid, Boronic acid, B-(4-bromo-2-thienyl)-, 3-Bromothiophene-5-boronic acid, Boronic acid, (4-bromo-2-thienyl)-

4-Bromothiophene-2-boronic acid

(4-Bromothiophen-2-yl)boronic acid

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CAS 499769-92-5: B-(4-Bromo-2-thienyl)boronic acid

4-Bromothiophene-2-boronic acid

Ref: 54-OR360816

(4-Bromothiophen-2-yl)boronic acid

Ref: 10-F338449

4-Bromothiophene-2-boronic acid

Ref: 3D-FB160584

3-BROMOTHIOPHENE-5-BORONIC ACID

Ref: IN-DA00D8UN