CAS 106009-19-2: 1H-Indole-2,3-dione, 5,7-dichloro-1-methyl-

Description: 1H-Indole-2,3-dione, 5,7-dichloro-1-methyl- is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of two chlorine atoms at the 5 and 7 positions of the indole ring contributes to its unique reactivity and potential biological activity. The methyl group at the 1 position further modifies its properties, influencing solubility and interaction with biological targets. This compound is typically classified as a heterocyclic aromatic compound, and its dione functional groups indicate the presence of two carbonyl (C=O) functionalities, which can participate in various chemical reactions, including nucleophilic attacks and hydrogen bonding. The compound may exhibit interesting pharmacological properties, making it a subject of research in medicinal chemistry. Its specific applications and behavior in biological systems would depend on further studies, including its synthesis, stability, and interaction with other molecules. As with many halogenated compounds, it may also exhibit unique environmental and toxicological characteristics.

Formula: C₉H₅Cl₂NO₂

5,7-Dichloro-1-methyl-1H-indole-2,3-dione

CAS: 106009-19-2

• Purity: 95.0%
• Molecular weight: 230.0399932861328

5,7-dichloro-1-methyl-1h-indole-2,3-dione

CAS: 106009-19-2

Versatile small molecule scaffold

• Formula: C₉H₅Cl₂NO₂
• Purity: Min. 95%
• Molecular weight: 230.04 g/mol