91099-21-7

Usage

General Description

2(1H)-Quinazolinone, 7-methoxy-4-(4-methoxyphenyl)- is a chemical compound with the molecular formula C16H14N2O3. It is a derivative of quinazolinone, a heterocyclic compound with potential pharmacological properties. The presence of methoxy groups in the compound's structure suggests that it may have potential applications as a pharmaceutical or biological agent, as methoxy groups can play a role in modulating the compound's solubility, bioavailability, and receptor interactions. Further research and investigation into the specific properties and potential uses of 2(1H)-Quinazolinone, 7-methoxy-4-(4-methoxyphenyl)- will be necessary to fully understand its potential impact and applications.

Upstream product

• 139-77-5 1-(3-methoxyphenyl)urea 
• 100-09-4 4-methoxybenzoic acid 
• 91099-02-4 1-(4-methoxybenzoyl)-3-(3-methoxyphenyl)urea 
• 536-90-3 m-Anisidine 
• 18908-07-1 3-methoxyphenyl isocyanate 

Downstream Products

• 204763-74-6 2-chloro-7-methoxy-4-(4-methoxyphenyl)quinazoline 

Relevant academic research and scientific papers

Structure and Dynamics of Hydrogen Chelates: Part 1. NMR-Spectroscopic Studies in the Quinazoline-2-acetonitrile Series

To get informations on both the structure and dynamics of hydrogen chelates 1 of heteroaromatic systems, a great variety of quinazoline-2-acelonitrile chelates were synthesized (see 2-4). Similarly to the situation of the corresponding H-chelates in the p

Central Nervous System Active Compounds. XIV On the Cyclization of N-Acyl-N'-arylureas

The cyclization of N-acyl-N'-arylureas in polyphosphoric acid has been reinvestigated.The product is not only the 4-substituted quinazolin-2(1H)-one as reported, but also contains the 2-acylaniline in major proportions.Two minor products have also been isolated.At 80 deg, an intermediate has been detected, the properties of which are consistent with it being the corresponding 2-acylphenylurea.Acyl ureas with strongly electron-withdrawing acyl groups from major amount of the corresponding anilide by the formal loss of cyanic acid.The application of this reaction tothe synthesis of quinazolinylphthalides has been investigated.