3-Iodoindole-2-carboxylic acid is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of an iodine atom at the 3-position of the indole ring and a carboxylic acid functional group at the 2-position contributes to its unique reactivity and properties. This compound is typically a solid at room temperature and is soluble in organic solvents, reflecting its aromatic nature. It may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of compounds with potential therapeutic applications. The iodine substituent can influence the compound's electronic properties and reactivity, while the carboxylic acid group can participate in hydrogen bonding and other interactions. As with many indole derivatives, 3-iodoindole-2-carboxylic acid may also serve as a building block in organic synthesis, allowing for the creation of more complex molecules. Safety data should be consulted for handling and storage, as with all chemical substances.

3-IODOINDOLE-2-CARBOXYLIC ACID

167631-58-5: 3-Iodoindole-2-carboxylic acid is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of an iodine atom at the 3-position of the indole ring and a carboxylic acid functional group at the 2-position contributes to its unique reactivity and properties. This compound is typically a solid at room temperature and is soluble in organic solvents, reflecting its aromatic nature. It may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of compounds with potential therapeutic applications. The iodine substituent can influence the compound's electronic properties and reactivity, while the carboxylic acid group can participate in hydrogen bonding and other interactions. As with many indole derivatives, 3-iodoindole-2-carboxylic acid may also serve as a building block in organic synthesis, allowing for the creation of more complex molecules. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 167631-58-5

3-IODOINDOLE-2-CARBOXYLIC ACID

1H-Indole-2-carboxylic acid, 3-iodo-

Ref: IN-DA001XI0

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

Ref: 54-OR110213

3-Iodoindole-2-carboxylic acid

Ref: 10-F023843