Produktname:4-Chloro-5-nitroquinazoline

IUPAC Name:4-chloro-5-nitroquinazoline

CAS:75224-28-1
Molekulare Formel:C8H4ClN3O2
Reinheit:95%
Katalognummer:CM216620
Molekulargewicht:209.59

Packungseinheit Verfügbarer Vorrat Preis($) Menge
CM216620-1g 1-2 Weeks ŵȡǶNJ

Nur für den Einsatz in Forschung und Entwicklung..

Anfrage-Formular

   refresh    

Produkt-Details

CAS-Nr.:75224-28-1
Molekulare Formel:C8H4ClN3O2
Schmelzpunkt:-
SMILES-Code:O=[N+](C1=CC=CC2=NC=NC(Cl)=C12)[O-]
Dichte:
Katalognummer:CM216620
Molekulargewicht:209.59
Siedepunkt:
Mdl-Nr.:MFCD18448299
Lagerung:

Category Infos

Quinazolines
Quinazolines belong to heterocyclic chemistry, also known as 1,3-naphthalenes. The backbone consists of two six-membered aromatic rings fused to each other, with two nitrogen atoms at positions 1 and 3 on the backbone. The presence of these two nitrogen atoms in quinazoline increases its importance in pharmaceutical and biological reactions. Quinazolines and their derivatives are among the most important heterocyclic compounds due to their diverse chemical reactivity and important range of biological activities.

Related Products



Product Other Information

Product Overview 4-Chloro-5-nitroquinazoline (4C5NQ) is a synthetic quinazoline compound that has been widely studied in recent years for its potential applications in the field of medicinal chemistry. 4C5NQ has been found to possess a variety of useful properties, including antifungal, antibacterial, antimalarial, and antiviral activity. Additionally, 4C5NQ has been studied for its potential use in the development of novel therapeutic agents and as a potential drug delivery system.
Synthesis and Application 4-Chloro-5-nitroquinazoline can be synthesized by a variety of methods, including the reaction of 4-chloro-5-nitrobenzaldehyde with hydrazine hydrate, the reaction of 4-chloro-5-nitrobenzaldehyde with ethylenediamine, and the reaction of 4-chloro-5-nitrobenzaldehyde with hydroxylamine hydrochloride. Additionally, 4-Chloro-5-nitroquinazoline can be synthesized through the reaction of 4-chloro-5-nitrobenzaldehyde with an aqueous solution of ammonium hydroxide. 4-Chloro-5-nitroquinazoline has been studied extensively for its potential applications in medicinal chemistry and drug delivery. 4-Chloro-5-nitroquinazoline has been found to possess antifungal, antibacterial, antimalarial, and antiviral activity, and has been studied for its potential use in the development of novel therapeutic agents. Additionally, 4-Chloro-5-nitroquinazoline has been studied for its potential use as a drug delivery system, as it can be used to deliver drugs directly to the site of action.
Future Directions Given the potential applications of 4-Chloro-5-nitroquinazoline in the field of medicinal chemistry, there are a number of potential future directions for research. These include further research into the exact mechanism of action of 4-Chloro-5-nitroquinazoline, the development of novel therapeutic agents based on 4-Chloro-5-nitroquinazoline, and the development of novel drug delivery systems based on 4-Chloro-5-nitroquinazoline. Additionally, further research could be conducted into the potential applications of 4-Chloro-5-nitroquinazoline in the field of cancer therapy, as well as its potential use as an anti-inflammatory agent.