4-Bromo-1H-indole-6-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. The presence of a bromine atom at the 4-position and a carboxylic acid group at the 6-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar solvents, such as water and alcohols, due to the carboxylic acid functionality. It may exhibit acidic behavior, capable of donating a proton from the carboxylic group. The bromine substituent can influence the compound's reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, 4-Bromo-1H-indole-6-carboxylic acid may have applications in medicinal chemistry and material science, particularly in the synthesis of biologically active compounds or as a building block in organic synthesis. Its specific properties, such as melting point and spectral data, can be determined through experimental methods.

4-Bromo-1H-indole-6-carboxylic acid

374633-27-9: 1H-indole-6-carboxylic acid, 4-bromo-, 4-Bromo-6-indolecarboxylic acid, 4-Bromoindole-6-carboxylic acid,  4-Bromo-1H-indole-6-carboxylic acid, 4-Bromo-1H-indole-6-carboxylic acid

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CAS 374633-27-9: 4-Bromo-1H-indole-6-carboxylic acid

4-Bromo-1H-indole-6-carboxylic acid

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4-Bromo-1H-indole-6-carboxylic acid

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4-Bromo-1H-indole-6-carboxylic acid

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4-Bromo-1H-indole-6-carboxylic acid

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