6-Nitro-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 nitro group at the 6-position and a carboxylic acid group at the 3-position contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. This compound is typically a yellow to orange crystalline solid, exhibiting moderate solubility in polar solvents such as water and ethanol. Its molecular structure allows for hydrogen bonding, which can influence its solubility and interaction with biological systems. The nitro group can participate in electrophilic substitution reactions, while the carboxylic acid group can act as a proton donor, making it a versatile building block in organic synthesis. Additionally, 6-Nitro-1H-indole-3-carboxylic acid may exhibit biological activity, although specific pharmacological properties would require further investigation. Safety data should be consulted for handling and storage, as with any chemical substance.

6-Nitro-1H-indole-3-carboxylic acid

10242-03-2: 1H-Indole-3-carboxylic acid, 6-nitro-, 6-Nitro-1H-Indole-3-Carboxylic Acid, Indole-3-carboxylic acid, 6-nitro-, NSC 82382

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CAS 10242-03-2: 6-Nitro-1H-indole-3-carboxylic acid

6-Nitro-1H-indole-3-carboxylic acid

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6-Nitro-1H-indole-3-carboxylic acid

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6-Nitroindole-3-carboxylic acid

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1H-Indole-3-carboxylic acid, 6-nitro-

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