3-Formyl-5,6-dimethoxy-1H-indole-2-carboxylic acid is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features a formyl group (-CHO) at the 3-position and carboxylic acid (-COOH) functionality at the 2-position, along with two methoxy groups (-OCH3) at the 5 and 6 positions of the indole ring. These substituents contribute to its chemical reactivity and potential biological activity. The presence of both electron-donating methoxy groups and electron-withdrawing formyl and carboxylic acid groups can influence the compound's acidity, solubility, and interaction with biological targets. It may exhibit properties such as antimicrobial or anti-inflammatory activity, making it of interest in medicinal chemistry. The compound's molecular structure allows for various synthetic modifications, which can be explored for developing derivatives with enhanced properties. As with many indole derivatives, it may also participate in various chemical reactions, including condensation and substitution reactions.

3-FORMYL-5,6-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID

858769-50-3: 3-Formyl-5,6-dimethoxy-1H-indole-2-carboxylic acid is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features a formyl group (-CHO) at the 3-position and carboxylic acid (-COOH) functionality at the 2-position, along with two methoxy groups (-OCH3) at the 5 and 6 positions of the indole ring. These substituents contribute to its chemical reactivity and potential biological activity. The presence of both electron-donating methoxy groups and electron-withdrawing formyl and carboxylic acid groups can influence the compound's acidity, solubility, and interaction with biological targets. It may exhibit properties such as antimicrobial or anti-inflammatory activity, making it of interest in medicinal chemistry. The compound's molecular structure allows for various synthetic modifications, which can be explored for developing derivatives with enhanced properties. As with many indole derivatives, it may also participate in various chemical reactions, including condensation and substitution reactions.

CAS 858769-50-3

3-FORMYL-5,6-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID