CAS 82050-10-0

3-(~2~H_3_)methyl-3H-imidazo[4,5-f]quinolin-2-amine

Description:

3-(2H3)methyl-3H-imidazo[4,5-f]quinolin-2-amine, with the CAS number 82050-10-0, is a chemical compound that belongs to the class of imidazoquinolines. This substance features a fused bicyclic structure that includes both imidazole and quinoline moieties, which contribute to its unique chemical properties. The presence of the methyl group at the 3-position of the imidazole ring indicates that it may exhibit specific steric and electronic characteristics, potentially influencing its reactivity and interactions with biological targets. Compounds of this type are often studied for their pharmacological properties, including potential applications in medicinal chemistry, such as in the development of anti-cancer or anti-inflammatory agents. The compound's molecular structure suggests it may engage in hydrogen bonding and π-π stacking interactions, which are important in biological systems. Additionally, its solubility, stability, and bioavailability would be critical factors in determining its practical applications in research and therapeutics.

Formula: C₁₁H₇D₃N₄

InChI: InChI=1/C11H10N4/c1-15-9-5-4-8-7(3-2-6-13-8)10(9)14-11(15)12/h2-6H,1H3,(H2,12,14)/i1D3

SMILES: C(n1c2ccc3c(cccn3)c2[nH]c1=N)([2H])([2H])[2H]

2-Amino-3-methyl-3H-imidazo[4,5-f]quinoline-d3

Controlled Product

CAS: 82050-10-0

Applications IQ is highly mutagenic in the Ames test. Investigations have shown that this compound may be present in broiled fish, fried beef, commercial beef extracts and protein pyrolysates.
References Ohgaki, H., et al.: Carcinogenesis, 5, 921 (1984), Stavric, B., et al.: Fd. Chem. Toxic., 31, 12, 981 (1993), Sugimura, T., et al.: Mutation Research, 290, 43 (1993), Eisenbrand & Tang: Toxicology, 84, 1 (1993), Josephy, P.D., et al.: Carcinogenesis, 16, 9, 2037 (1995),

Formula: C₁₁₂H₃H₇N₄

Color and Shape: Yellow-Brown Solid

Molecular weight: 201.24

Ref: TR-A616720