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CAS 913835-91-3

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4-boronothiophene-2-carboxylic acid

Description:
4-Boronothiophene-2-carboxylic acid is an organoboron compound characterized by the presence of a boron atom attached to a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylic acid functional group (-COOH) at the 2-position of the thiophene ring, contributing to its acidic properties. The boron atom typically enhances the compound's reactivity and can facilitate various chemical transformations, making it useful in organic synthesis and materials science. The presence of both the boron and the carboxylic acid groups allows for potential applications in catalysis, organic electronics, and as a building block in the synthesis of more complex molecules. Additionally, the thiophene ring can impart interesting electronic properties, making this compound of interest in the development of conductive polymers and organic semiconductors. Overall, 4-boronothiophene-2-carboxylic acid is a versatile compound with significant implications in both academic research and industrial applications.
Formula:C5H5BO4S
InChI:InChI=1/C5H5BO4S/c7-5(8)4-1-3(2-11-4)6(9)10/h1-2,9-10H,(H,7,8)
SMILES:c1c(csc1C(=O)O)B(O)O
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