CAS 130570-60-4

1H-Indol-6-ol, 1-methyl-

Description:

1H-Indol-6-ol, 1-methyl- (CAS 130570-60-4) is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a hydroxyl group (-OH) at the 6-position and a methyl group (-CH3) at the 1-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. Its indole framework is known for its biological significance, often serving as a precursor to various natural products and pharmaceuticals. The compound may exhibit various functional properties, including potential antioxidant and antimicrobial activities, making it of interest in medicinal chemistry and drug development. Additionally, its reactivity can be influenced by the presence of the hydroxyl and methyl groups, allowing for further chemical modifications. Overall, 1H-Indol-6-ol, 1-methyl- is a compound of interest in both synthetic and medicinal chemistry contexts.

Formula: C₉H₉NO

Carbazochrome Impurity 6

CAS: 130570-60-4

Formula: C₉H₉NO

Molecular weight: 147.18

Ref: 4Z-C-163009

1-Methyl-1H-indol-6-ol

Controlled Product

CAS: 130570-60-4

Formula: C₉H₉NO

Color and Shape: Neat

Molecular weight: 147.174

Ref: TR-M324930

1-Methyl-1H-indol-6-ol

CAS: 130570-60-4

1-Methyl-1H-indol-6-ol is a coupler that is used in the production of polymers. It is a sequential, c1-4 alkyl alkoxycarbonyl compound. 1-Methyl-1H-indol-6-ol can be oxidized to form an N-(C1-4 alkyl) indole and CO2, which reacts with other monomers to produce polymers. This chemical has been shown to have keratinase activity and can be used for the oxidation of human hair keratin fibres.

Formula: C₉H₉NO

Purity: Min. 95%

Molecular weight: 147.17 g/mol

Ref: 3D-FFA57060