1026963-18-7

Basic information

• Product Name: Phosphoric acid 4-(3,4-dimethoxy-benzyl)-6-fluoro-3-oxo-3,4-dihydro-quinoxalin-2-yl ester diethyl ester
• Synonyms: Phosphoric acid 4-(3,4-dimethoxy-benzyl)-6-fluoro-3-oxo-3,4-dihydro-quinoxalin-2-yl ester diethyl ester
• CAS NO: 1026963-18-7
• Molecular Weight: 466.403
• Mol File: 1026963-18-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Phosphoric acid 4-(3,4-dimethoxy-benzyl)-6-fluoro-3-oxo-3,4-dihydro-quinoxalin-2-yl ester diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphoric acid 4-(3,4-dimethoxy-benzyl)-6-fluoro-3-oxo-3,4-dihydro-quinoxalin-2-yl ester diethyl ester(1026963-18-7)
• EPA Substance Registry System: Phosphoric acid 4-(3,4-dimethoxy-benzyl)-6-fluoro-3-oxo-3,4-dihydro-quinoxalin-2-yl ester diethyl ester(1026963-18-7)

Safety Data

• Hazardous Substances Data: 1026963-18-7(Hazardous Substances Data)

Upstream product

• 1026026-68-5 (3,4-Dimethoxy-benzyl)-(5-fluoro-2-nitro-phenyl)-amine 
• 1026954-54-0 N²-(3,4-Dimethoxy-benzyl)-4-fluoro-benzene-1,2-diamine 
• 814-49-3 diethyl chlorophosphate 
• 1026407-10-2 1-(3,4-Dimethoxy-benzyl)-7-fluoro-1,4-dihydro-quinoxaline-2,3-dione 
• 2106-50-5 2-chloro-4-fluoro-1-nitrobenzene 
• 5763-61-1 3,4-dimethoxybenzylamine 

Downstream Products

• 1026071-37-3 5-(3,4-Dimethoxy-benzyl)-7-fluoro-3-(4-fluoro-phenyl)-4,5-dihydro-imidazo[1,5-a]quinoxaline 
• 148891-12-7 (3,5-Dimethyl-piperazin-1-yl)-[7-fluoro-3-(4-fluoro-phenyl)-4H-imidazo[1,5-a]quinoxalin-5-yl]-methanone 
• 180207-99-2 7-Fluoro-3-(4-fluoro-phenyl)-4,5-dihydro-imidazo[1,5-a]quinoxaline 
• 1026965-28-5 5-(3,4-Dimethoxy-benzyl)-7-fluoro-3-(4-fluoro-phenyl)-5H-imidazo[1,5-a]quinoxalin-4-one 

Relevant articles and documents

3-Phenyl-substituted imidazo[1,5-a]quinoxalin-4-ones and imidazo[1,5- a]quinoxaline ureas that have high affinity at the GABA(A)/benzodiazepine receptor complex

A series of imidazo[1,5-a]quinoxalin-4-ones and imidazo[1,5- a]quinoxaline ureas containing substituted phenyl groups at the 3-position was developed. Compounds within the imidazo-[1,5-a]quinoxaline urea series had high affinity for the GABA(A)/benzodiaze