CAS 89324-44-7
:3-Thiophenecarboxylic acid, 5-formyl-
Description:
3-Thiophenecarboxylic acid, 5-formyl- is an organic compound characterized by the presence of both a thiophene ring and a carboxylic acid functional group. The thiophene ring, a five-membered aromatic heterocycle containing sulfur, contributes to the compound's unique electronic properties and reactivity. The presence of the formyl group (–CHO) at the 5-position of the thiophene ring introduces an aldehyde functionality, which can participate in various chemical reactions, such as condensation and oxidation. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its chemical properties make it of interest in organic synthesis and materials science, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the compound's structure allows for potential applications in the field of organic electronics and as a building block for more complex molecules. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C6H4O3S
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Found 4 products.
3-Thiophenecarboxylic acid, 5-formyl-
CAS:Formula:C6H4O3SPurity:97%Color and Shape:SolidMolecular weight:156.15925-Formylthiophene-3-carboxylic acid
CAS:5-Formylthiophene-3-carboxylic acidPurity:97%Molecular weight:156.16g/mol5-Formylthiophene-3-carboxylic acid
CAS:<p>5-Formylthiophene-3-carboxylic acid is an inhibitor of the cycloaddition reaction between azomethine and enamines. It has been shown to be diastereoselective, inhibiting the formation of the undesired enantiomer. The synthesis and characterization of this compound has been used in process research for drug discovery.</p>Formula:C6H4O3SPurity:Min. 95%Molecular weight:156.16 g/mol
