1H-Indole, 2-iodo-1-methyl- is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a methyl group at the 1-position and an iodine atom at the 2-position distinguishes it from other indole derivatives. This compound typically exhibits a pale yellow to brownish color and is soluble in organic solvents. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to the biological activity associated with indole derivatives. The iodine substituent can enhance the compound's reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, 1H-Indole, 2-iodo-1-methyl- may exhibit fluorescence properties, which can be advantageous in analytical applications. As with many halogenated compounds, it is essential to handle this substance with care, considering potential toxicity and environmental impact. Proper safety protocols should be followed when working with this compound in laboratory settings.

1H-Indole, 2-iodo-1-methyl-

75833-63-5: 1H-Indole, 2-iodo-1-methyl- is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a methyl group at the 1-position and an iodine atom at the 2-position distinguishes it from other indole derivatives. This compound typically exhibits a pale yellow to brownish color and is soluble in organic solvents. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to the biological activity associated with indole derivatives. The iodine substituent can enhance the compound's reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, 1H-Indole, 2-iodo-1-methyl- may exhibit fluorescence properties, which can be advantageous in analytical applications. As with many halogenated compounds, it is essential to handle this substance with care, considering potential toxicity and environmental impact. Proper safety protocols should be followed when working with this compound in laboratory settings.

CAS 75833-63-5

1H-Indole, 2-iodo-1-methyl-