CAS 1451393-26-2
:3-Bromo-2-formylthiophene-5-boronic acid
Description:
3-Bromo-2-formylthiophene-5-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, a bromine atom, and a thiophene ring with a formyl substituent. This compound typically exhibits properties associated with both boronic acids and heterocyclic aromatic compounds. The boronic acid group allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and materials science. The presence of the bromine atom enhances its reactivity and can serve as a useful handle for further functionalization. The thiophene ring contributes to the compound's electronic properties, potentially allowing for applications in organic electronics or as a building block in the synthesis of more complex molecules. Additionally, the formyl group introduces a reactive aldehyde functionality, which can participate in condensation reactions. Overall, 3-Bromo-2-formylthiophene-5-boronic acid is a versatile compound with potential applications in pharmaceuticals, agrochemicals, and advanced materials.
Formula:C5H4BBrO3S
Synonyms:- (4-bromo-5-formylthiophen-2-yl)boronic acid
- 3-Bromo-2-formylthiophene-5-boronic acid
- Boronic acid, B-(4-bromo-5-formyl-2-thienyl)-
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