CAS 76180-97-7

1H-Imidazo[4,5-f]quinolin-2-amine

Description:

1H-Imidazo[4,5-f]quinolin-2-amine is a heterocyclic organic compound characterized by its fused imidazole and quinoline rings, which contribute to its unique chemical properties. This compound typically exhibits a planar structure, allowing for effective π-π stacking interactions, which can influence its biological activity. It is often studied for its potential pharmacological applications, particularly in the fields of medicinal chemistry and drug development, due to its ability to interact with various biological targets. The presence of an amino group at the 2-position enhances its reactivity and solubility in polar solvents. Additionally, this compound may exhibit fluorescence properties, making it useful in biochemical assays. Its molecular structure allows for various substitution patterns, which can be explored to optimize its activity and selectivity. Overall, 1H-Imidazo[4,5-f]quinolin-2-amine represents a significant scaffold in the development of novel therapeutic agents.

Formula: C₁₀H₈N₄

InChI: InChI=1S/C10H8N4/c11-10-13-8-4-3-7-6(9(8)14-10)2-1-5-12-7/h1-5H,(H3,11,13,14)

InChI key: InChIKey=GSLMSTTZNJHJRA-UHFFFAOYSA-N

SMILES: NC=1NC=2C=3C(C=CC2N1)=NC=CC3

Synonyms:

• 2-Aminoimidazo[4,5-f]quinoline
• 2-Amino-3H-imidazo[4,5-f]quinoline
• 1H-Imidazo[4,5-f]quinolin-2-amine

2-Aminoimidazo[4,5-f]quinoline Dihydrochloride

Controlled Product

CAS: 76180-97-7

Applications 2-Aminoimidazo[4,5-f]quinoline Dihydrochloride, is a metabolite of the carcinogen 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), (A616500).
References Barnes, W., et al.: Carcinogenesis, 6, 441 (1985), Inamasu, T., et al.: Food Chem. Toxicol., 27, 369 (1989), Stiborova, M., et al.: Cancer Res., 64, 8374 (2004), Armbrecht, H., et al.: Drug Metab. Dispos., 35, 633 (2007),

Formula: C₁₀H₈N₄·2HCl

Color and Shape: Neat

Molecular weight: 257.12

Ref: TR-A611683