4-Iodo-2,3-dihydro-1H-indole 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 the iodine atom at the 4-position of the indole ring significantly influences its chemical reactivity and properties. This compound typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its ability to interact with biological targets. The dihydro form indicates that it has two hydrogen atoms added to the indole structure, which can affect its stability and reactivity. Additionally, the iodine substituent can enhance the compound's lipophilicity, potentially improving its bioavailability. As with many halogenated compounds, it may exhibit unique electronic properties, making it a subject of interest in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety and handling precautions are essential due to the potential toxicity associated with iodine-containing compounds.

4-iodo-2,3-dihydro-1H-indole

62108-16-1: 4-Iodo-2,3-dihydro-1H-indole 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 the iodine atom at the 4-position of the indole ring significantly influences its chemical reactivity and properties. This compound typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its ability to interact with biological targets. The dihydro form indicates that it has two hydrogen atoms added to the indole structure, which can affect its stability and reactivity. Additionally, the iodine substituent can enhance the compound's lipophilicity, potentially improving its bioavailability. As with many halogenated compounds, it may exhibit unique electronic properties, making it a subject of interest in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety and handling precautions are essential due to the potential toxicity associated with iodine-containing compounds.

CAS 62108-16-1

4-iodo-2,3-dihydro-1H-indole

4-Methylindoline

Ref: IN-DA003LS4

4-Methyl-2,3-dihydro-1H-indole

Ref: 54-OR928566

4-Methylindoline

Ref: 10-F318325

4-Methylindoline

Ref: 3D-MCA10816