CAS 2446-62-0
:11H-Pyrido[2,1-b]quinazolin-11-one, 6,7,8,9-tetrahydro-
Description:
11H-Pyrido[2,1-b]quinazolin-11-one, 6,7,8,9-tetrahydro- is a heterocyclic organic compound characterized by its fused pyridine and quinazoline structures. This compound features a bicyclic framework that includes a pyridine ring and a quinazoline moiety, contributing to its potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of nitrogen atoms in its structure can influence its reactivity and interaction with biological systems, making it of interest in medicinal chemistry. Compounds of this type are often investigated for their pharmacological properties, including potential anti-cancer, anti-inflammatory, or antimicrobial activities. The specific stereochemistry and substituents can significantly affect the compound's properties and biological effects. As with many heterocycles, the electronic properties and steric factors play crucial roles in determining the compound's reactivity and interactions with other molecules. Safety data and handling precautions should be considered, as with any chemical substance, particularly in laboratory settings.
Formula:C12H12N2O
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Found 3 products.
6H,7H,8H,9H,11H-Pyrido[2,1-b]quinazolin-11-one
CAS:<p>6H,7H,8H,9H,11H-Pyrido[2,1-b]quinazolin-11-one is a biomolecular compound that belongs to the class of aminophenols. It is synthesized by the oxidative coupling of deoxyvasicinone with sodium hypochlorite and irradiation. The reaction time for this reaction is 10 minutes at room temperature. 6H,7H,8H,9H,11H-Pyrido[2,1-b]quinazolin-11-one has been shown to have antimicrobial activity against bacteria and fungi in vitro. Its structure is similar to mackinazolinone and synthetic analogues such as 2-(4'-aminophenyl)thiazole. 6H,7H,8H,9H,11H-Pyrido[2,1-b]quinazolin-11-one also reacts with dien</p>Formula:C12H12N2OPurity:Min. 95%Molecular weight:200.24 g/mol


