CAS 3468-22-2

N-Methyl-1H-indole-4-methanamine

Description:

N-Methyl-1H-indole-4-methanamine, with the CAS number 3468-22-2, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a methyl group attached to the nitrogen atom of the indole, as well as a methanamine group at the 4-position of the indole ring. It is typically a colorless to pale yellow liquid or solid, depending on its form and purity. The presence of the amine functional group suggests that it may exhibit basic properties and can participate in hydrogen bonding, influencing its solubility in polar solvents. N-Methyl-1H-indole-4-methanamine may have applications in medicinal chemistry and research due to its structural similarity to biologically active compounds. However, specific information regarding its reactivity, stability, and potential applications would require further investigation, including safety data and handling precautions, as with any chemical substance.

Formula: C₁₀H₁₂N₂

InChI: InChI=1S/C10H12N2/c1-11-7-8-3-2-4-10-9(8)5-6-12-10/h2-6,11-12H,7H2,1H3

InChI key: InChIKey=DPXOSZVHVILMJI-UHFFFAOYSA-N

SMILES: C(NC)C1=C2C(NC=C2)=CC=C1

Synonyms:

• 1H-Indole-4-methanamine, N-methyl-
• Indole, 4-[(methylamino)methyl]-
• 1-(1H-Indol-4-yl)-N-methylmethanamine
• N-Methyl-1H-indole-4-methanamine
• [(1H-Indol-4-yl)methyl]methylamine

[(1H-Indol-4-yl)methyl](methyl)amine

CAS: 3468-22-2

[(1H-Indol-4-yl)methyl](methyl)amine is a substituted isoquinoline. It has been shown to be an effective inhibitor of the enzyme allyl alcohol dehydrogenase, which catalyzes the conversion of allyl alcohol to acetaldehyde. The reduction of [(1H-indol-4-yl)methyl]-(methyl)amine can be accomplished with either a Grignard reagent or a reductive alkylation.

Formula: C₁₀H₁₂N₂

Purity: Min. 95%

Molecular weight: 160.22 g/mol

Ref: 3D-DAA46822