4-Chloro-6-methyl-1H-indole is an organic compound that belongs to the indole family, characterized by a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. This compound features a chlorine atom at the 4-position and a methyl group at the 6-position of the indole structure, which influences its chemical reactivity and biological properties. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the chlorine atom can enhance its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Additionally, compounds like 4-Chloro-6-methyl-1H-indole are of interest in medicinal chemistry due to their potential pharmacological activities, including antimicrobial and anticancer properties. Its synthesis often involves multi-step organic reactions, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or environmental impact.

4-Chloro-6-methyl-1H-indole

885521-78-8: 4-Chloro-6-methyl-1H-indole is an organic compound that belongs to the indole family, characterized by a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. This compound features a chlorine atom at the 4-position and a methyl group at the 6-position of the indole structure, which influences its chemical reactivity and biological properties. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the chlorine atom can enhance its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. Additionally, compounds like 4-Chloro-6-methyl-1H-indole are of interest in medicinal chemistry due to their potential pharmacological activities, including antimicrobial and anticancer properties. Its synthesis often involves multi-step organic reactions, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or environmental impact.

CAS 885521-78-8

4-Chloro-6-methyl-1H-indole

4-Chloro-6-methyl-1H-indole

Ref: IN-DA00IF6Z

4-Chloro-6-methyl-1H-indole

Ref: 54-OR72987

4-Chloro-6-methyl-1H-indole

Ref: 10-F337444