1140627-77-5

Basic information

• Product Name: EAPB₅₀₃
• Synonyms: EAPB₅₀₃
• CAS NO: 1140627-77-5
• Molecular Weight: 304.351
• Mol File: 1140627-77-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: EAPB₅₀₃(CAS DataBase Reference)
• NIST Chemistry Reference: EAPB₅₀₃(1140627-77-5)
• EPA Substance Registry System: EAPB₅₀₃(1140627-77-5)

Safety Data

• Hazardous Substances Data: 1140627-77-5(Hazardous Substances Data)

Upstream product

• 191349-69-6 4-chloroimidazo[1,2-a]quinoxaline 
• 133307-45-6 imidazo[1,2-a]quinoxaline-4-(5H)-one 
• 82173-01-1 N-(2-Fluorophenyl)-1H-imidazol-2-carboxamide 
• 1140627-75-3 1-bromo-N-methylimidazo[1,2-a]-quinoxalin-4-amine 
• 10365-98-7 3-methoxyphenylboronic acid 

Downstream Products

• 1140627-83-3 EAPB₆₀₃ 

Relevant articles and documents

Fluorescence Study of Imidazoquinoxalines

The fluorescence properties of eleven novel derivatives based on the imidazo[1,2-a]quinoxaline structures have been studied. The absorption and emission spectra of these compounds have been recorded in dimethylsulfoxide solution. The phenyl substituting group on position 1 gives them particular properties thanks to the diverse hydroxy or methoxy decorating moieties, especially when they are multiplied or mixed. The investigated fluorescence auto-quenching revealed that the decreasing fluorescence intensity correlated only with the chemical structures of the aromatic compounds.

New imidazo[1,2-a]quinoxaline derivatives: Synthesis and in vitro activity against human melanoma

New imidazo[1,2-a]quinoxaline analogues have been synthesized in good yields via a bimolecular condensation of 2-imidazole carboxylic acid, followed by a coupling with ortho-fluoroaniline and subsequent substitution on the imidazole ring by Suzuki Cross-c