2-Chloro-1H-indole-3-carboxylic acid is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a carboxylic acid group (-COOH) at the 3-position and a chlorine atom at the 2-position of the indole ring contributes to its unique chemical properties. This compound is typically a white to off-white solid and is soluble in polar solvents, such as water and alcohols, due to the carboxylic acid functionality. It exhibits acidic behavior, capable of donating a proton in solution. The chlorine substituent can influence the compound's reactivity and biological activity, making it of interest in medicinal chemistry and drug development. Additionally, 2-chloro-1H-indole-3-carboxylic acid may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in synthetic organic chemistry. Its specific applications and biological activities can vary, but it is often explored for potential therapeutic uses.

2-chloro-1H-indole-3-carboxylic acid

54778-20-0: 1H-indole-3-carboxylic acid, 2-chloro-,  2-Chloro-1H-indole-3-carboxylic acid

2-Chloro-1H-indole-3-carboxylic acid

2-Chloro-1H-indole-3-carboxylic acid is an antiinflammatory drug that belongs to the class of indomethacin. It is a nonsteroidal antiinflammatory drug that is used for the treatment of inflammation and pain. 2-Chloro-1H-indole-3-carboxylic acid has been shown to inhibit carrageenin induced paw edema in rats, suggesting its potential as a novel antiinflammatory agent.

CAS 54778-20-0: 2-chloro-1H-indole-3-carboxylic acid

2-Chloro-1H-indole-3-carboxylic acid

Ref: 10-F066300

2-Chloro-1H-indole-3-carboxylic acid

Ref: 3D-FC56653

2-CHLORO-1H-INDOLE-3-CARBOXYLIC ACID

Ref: IN-DA00D8W8

2-Chloro-1H-indole-3-carboxylic acid

Ref: 54-OR305201