89938-22-7

Basic information

• Product Name: 6-CHLORO-3,4-DIHYDRO-2(1H)-QUINOXALINONE
• Synonyms: 6-CHLORO-3,4-DIHYDRO-2(1H)-QUINOXALINONE;6-Chloro-3,4-dihydroquinoxalin-2(1H)-one
• CAS NO: 89938-22-7
• Molecular Formula: C₈H₇ClN₂O
• Molecular Weight: 182.607
• Mol File: 89938-22-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 386.8°Cat760mmHg
• Flash Point: 187.7°C
• Appearance: /
• Density: 1.335g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 6-CHLORO-3,4-DIHYDRO-2(1H)-QUINOXALINONE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-CHLORO-3,4-DIHYDRO-2(1H)-QUINOXALINONE(89938-22-7)
• EPA Substance Registry System: 6-CHLORO-3,4-DIHYDRO-2(1H)-QUINOXALINONE(89938-22-7)

Safety Data

• Hazardous Substances Data: 89938-22-7(Hazardous Substances Data)

Usage

General Description

6-CHLORO-3,4-DIHYDRO-2(1H)-QUINOXALINONE, also known as quinoline-3,4-dione, is a chemical compound with the molecular formula C9H6ClNO2. It is a chlorinated derivative of quinoxalinone, with a chlorine atom attached to the sixth carbon of the quinoxaline ring. 6-CHLORO-3,4-DIHYDRO-2(1H)-QUINOXALINONE has been studied for its potential biological and pharmacological properties, including its use as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has been reported to exhibit antibacterial and antifungal activities, as well as potential anti-inflammatory and antitumor properties. 6-CHLORO-3,4-DIHYDRO-2(1H)-QUINOXALINONE is a versatile compound with potential applications in the pharmaceutical and agricultural industries.

Upstream product

• 2427-71-6 6-chloro-1,2-dihydroquinoxalin-2-one 
• 700-37-8 4-chloro-2-fluoro-nitrobenzene 
• 610-40-2 3,4-dinitro-chlorobenzene 
• 34797-69-8 p-chloro-o-nitroacetoacetanilide 
• 95-83-0 4-Chloro-1,2-phenylenediamine 
• 34836-97-0 6-chloro-1,2-dihydro-2-oxoquinoxaline 4-oxide 
• 859307-61-2 ethyl 2-(4-chloro-2-nitrophenylamino)acetate 

Downstream Products

• 463-72-9 carbamic chloride 
• 18671-97-1 2,6-dichloroquinoxaline 

Relevant articles and documents

Palladium-catalyzed direct Hiyama arylation of quinoxalin-2(1H)-ones with aryl siloxanes in water

An efficient method for palladium-catalyzed direct Hiyama coupling of various quinoxalin-2(1H)-ones with aryl siloxanes has been developed. The protocol provides a convenient access to a variety of useful C3-arylated 1-methylquinoxalin-2(1H)-one derivatives in reasonable yields by using low cost water as a solvent and oxygen as an oxidant.

High-affinity partial agonist imidazo[1,5-a]quinoxaline amides, carbamates, and ureas at the γ-aminobutyric acid A/benzodiazepine receptor complex

A series of imidazo[1,5-a]quinoxaline amides, carbamates, and ureas which have high affinity for the γ-aminobutyric acid A/benzodiazepine receptor complex was developed. Compounds within this class have varying efficacies ranging from antagonists to full

The facile one pot synthesis of 6-substituted 2(1H)-quinoxalinones

Facile one pot synthesis of 6-substituted 2(1H)-quinoxalinones and these reaction mechanisms are described.The intramolecular cyclization reaction of 4'-substituted 2'-nitroacetoacetanilides in aqueous basic medium and the reduction of 6-substituted 2(1H)-quinoxalinone-4-oxide wit sodium borohydride or sodium hydrogensulfite were studied in detail