1H-Indole, 5-methoxy-6-methyl- (CAS 3139-10-4) is an organic compound belonging to the indole family, characterized by a bicyclic structure that includes a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This compound features a methoxy group (-OCH3) at the 5-position and a methyl group (-CH3) at the 6-position of the indole ring, which influences its chemical properties and reactivity. It is typically a colorless to pale yellow solid or liquid, depending on its purity and form. The presence of the methoxy and methyl substituents can enhance its lipophilicity, potentially affecting its biological activity and solubility in organic solvents. 1H-Indole derivatives are of significant interest in medicinal chemistry due to their diverse pharmacological properties, including anti-inflammatory, antimicrobial, and anticancer activities. The compound's stability, reactivity, and interactions with biological systems make it a subject of study in various fields, including organic synthesis and drug development.

1H-Indole, 5-methoxy-6-methyl-

3139-10-4: 1H-Indole, 5-methoxy-6-methyl- (CAS 3139-10-4) is an organic compound belonging to the indole family, characterized by a bicyclic structure that includes a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This compound features a methoxy group (-OCH3) at the 5-position and a methyl group (-CH3) at the 6-position of the indole ring, which influences its chemical properties and reactivity. It is typically a colorless to pale yellow solid or liquid, depending on its purity and form. The presence of the methoxy and methyl substituents can enhance its lipophilicity, potentially affecting its biological activity and solubility in organic solvents. 1H-Indole derivatives are of significant interest in medicinal chemistry due to their diverse pharmacological properties, including anti-inflammatory, antimicrobial, and anticancer activities. The compound's stability, reactivity, and interactions with biological systems make it a subject of study in various fields, including organic synthesis and drug development.

CAS 3139-10-4

1H-Indole, 5-methoxy-6-methyl-

6-Methyl-5-Methoxy indole

Ref: IN-DA00CARI

5-Methoxy-6-methyl-1H-indole

Ref: 54-OR1076576

5-Methoxy-6-methyl-1H-indole

Ref: 10-F243842