CAS 22259-53-6

Indole-3-methanamine

Description:

Indole-3-methanamine, with the CAS number 22259-53-6, is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features an amine group (-NH2) attached to the methylene (-CH2-) carbon of the indole, making it a derivative of indole. Indole-3-methanamine is typically a colorless to pale yellow solid or liquid, depending on its purity and form. It is soluble in polar solvents such as water and alcohols, owing to the presence of the amine group, which can engage in hydrogen bonding. This compound is of interest in various fields, including medicinal chemistry, due to its potential biological activities, including effects on neurotransmitter systems. Additionally, it may serve as an intermediate in the synthesis of more complex organic molecules. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₉H₁₀N₂

InChI: InChI=1/C9H10N2/c10-5-7-6-11-9-4-2-1-3-8(7)9/h1-4,6,11H,5,10H2

InChI key: InChIKey=JXYGLMATGAAIBU-UHFFFAOYSA-N

SMILES: C(N)C=1C=2C(NC1)=CC=CC2

Synonyms:

• (1H-Indol-3-Yl)Methanamine
• 1-(1H-indol-3-yl)methanamine
• 1H-Indol-3-ylmethanamine
• 1H-Indole-3-methanamine
• 3-(Aminomethyl)indole
• 3-Indoylmethanamine
• 3-Methyl-1H-indol-1-amine
• Indole, 3-(aminomethyl)-
• Indole-3-methanamine
• RARECHEM AL BW 0382
• (1H-INDOL-3-YL)METHANAMINE, 95+%
• 1H-INDOL-3-YLMETHYLAMINE

1H-Indole-3-methanamine

CAS: 22259-53-6

Formula: C₉H₁₀N₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 146.1891

Ref: IN-DA00I4DQ

3-Aminomethylindole

CAS: 22259-53-6

3-Aminomethylindole

Purity: 95%

Molecular weight: 146.19g/mol

Ref: 54-OR1010904

(1H-Indol-3-yl)methanamine

CAS: 22259-53-6

Indol-3-ylmethanamine is a plant hormone that belongs to the group of indole alkaloids. It inhibits the production of phytoalexins, which are secondary metabolites that protect plants against pathogens. Indol-3-ylmethanamine induces signal pathways and enzyme activities in cells, including hydroxylase activity and polyphenol oxidase activity. Indol-3-ylmethanamine has been shown to be active against 5-HT4 receptors in vitro.

Formula: C₉H₁₀N₂

Color and Shape: Powder

Molecular weight: 146.19 g/mol

Ref: 3D-FI139336

(1H-Indol-3-yl)methanamine

CAS: 22259-53-6

Formula: C₉H₁₀N₂

Purity: 95%

Color and Shape: Solid, Red powder

Molecular weight: 146.193

Ref: 10-F078831

Indole-3-methanamine

CAS: 22259-53-6

Indole-3-methanamine has been detected, but not quantified in, barley, cereals, and cereal products.

Formula: C₉H₁₀N₂

Purity: 99.69%

Color and Shape: Solid

Molecular weight: 146.19

Ref: TM-T19373

(1H-Indol-3-yl)methanamine

Controlled Product

CAS: 22259-53-6

Applications (1H-Indol-3-yl)methanamine is an indolic Tryptophan-derived metabolite with antifungal defense properties against Arabidopsis mlo2 mutant.
References Consonni, C., et al.: Plant Physiol., 152, 1544 (2010), Mahboobi, S., et al.: Archiv der Pharmazie , 327, 105 (1994)

Formula: C₉H₁₀N₂

Color and Shape: Neat

Molecular weight: 146.189

Ref: TR-I630028