123464-58-4

Basic information

• Product Name: 2-phenyl-7-fluoroquinoxaline
• Synonyms: 2-phenyl-7-fluoroquinoxaline
• CAS NO: 123464-58-4
• Molecular Weight: 224.237
• Mol File: 123464-58-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-phenyl-7-fluoroquinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-7-fluoroquinoxaline(123464-58-4)
• EPA Substance Registry System: 2-phenyl-7-fluoroquinoxaline(123464-58-4)

Safety Data

• Hazardous Substances Data: 123464-58-4(Hazardous Substances Data)

Upstream product

• 367-31-7 4-fluoro-1,2-phenylenediamine 
• 122-78-1 phenylacetaldehyde 
• 1074-12-0 phenylglyoxal hydrate 

Downstream Products

• 1296867-36-1 C₁₆H₁₁FN₂O₂ 
• 131706-08-6 7-Fluoro-2-phenyl-quinoxaline 4-oxide 
• 131705-95-8 7-Fluoro-2-phenyl-quinoxaline 1,4-dioxide 

Relevant articles and documents

Et3N-catalyzed oxidative dehydrogenative coupling of α-unsubstituted aldehydes and ketones with aryl diamines leading to quinoxalines using molecular oxygen as oxidant

A novel Et3N-catalyzed oxidative dehydrogenative coupling of α-unsubstituted carbonyl compounds with aryl diamines leading to quinoxaline derivatives using molecular oxygen as oxidant has been developed. Six hydrogen dissociations involving 2 sp3 C-H bonds activation are realized under mild conditions in this approach. Plausible mechanism is proposed for this novel Et3N-catalyzed transformation on the basis of the aboratively designed mechanistic studies including the radical detection by EPR. 2012 Elsevier Science. All rights reserved.

2-Phenyl-(6(7)-R-substituted quinoxalines N-oxides. Synthesis, structure elucidation and antimicrobial activity

A certain number of isomeric 2-phenylquinoxalines N-oxides bearing substituents at position 6/7 were prepared in order to investigate anti-microbial activity. The effect of some electron-withdrawing groups seem to increase an anti-Trichomonas vaginalis ac