5-Methoxy-1-methyl-1H-indole, with the CAS number 2521-13-3, is an organic compound belonging to the indole family, characterized by a fused bicyclic structure containing a benzene ring and a pyrrole ring. This compound features a methoxy group (-OCH3) at the 5-position and a methyl group (-CH3) at the 1-position of the indole structure, which influences its chemical reactivity and biological properties. It is typically a colorless to pale yellow solid or liquid, depending on its purity and form. The presence of the methoxy group can enhance its lipophilicity, potentially affecting its solubility in organic solvents. 5-Methoxy-1-methyl-1H-indole is of interest in various fields, including medicinal chemistry and pharmacology, due to its potential psychoactive properties and interactions with biological systems. Its synthesis can involve methods such as alkylation and methoxylation of indole derivatives. As with many indole derivatives, it may exhibit fluorescence and has been studied for its role in various biochemical pathways.

5-methoxy-1-methyl-1H-indole

2521-13-3: 5-Methoxy-1-methyl-1H-indole, with the CAS number 2521-13-3, is an organic compound belonging to the indole family, characterized by a fused bicyclic structure containing a benzene ring and a pyrrole ring. This compound features a methoxy group (-OCH3) at the 5-position and a methyl group (-CH3) at the 1-position of the indole structure, which influences its chemical reactivity and biological properties. It is typically a colorless to pale yellow solid or liquid, depending on its purity and form. The presence of the methoxy group can enhance its lipophilicity, potentially affecting its solubility in organic solvents. 5-Methoxy-1-methyl-1H-indole is of interest in various fields, including medicinal chemistry and pharmacology, due to its potential psychoactive properties and interactions with biological systems. Its synthesis can involve methods such as alkylation and methoxylation of indole derivatives. As with many indole derivatives, it may exhibit fluorescence and has been studied for its role in various biochemical pathways.

CAS 2521-13-3

5-methoxy-1-methyl-1H-indole

5-Methoxy-1-methylindole

Ref: IN-DA002QY3

5-Methoxy-1-methyl-1H-indole

Ref: 54-OR111390

5-Methoxy-1-methyl-1H-indole

Ref: 10-F430507