143814-63-5

Basic information

• Product Name: Benzene, 1,4-dimethoxy-2-nitro-3-(2-nitroethenyl)-, (E)-
• CAS NO: 143814-63-5
• Molecular Formula: C10H10N2O6
• Molecular Weight: 254.199
• Mol File: 143814-63-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1,4-dimethoxy-2-nitro-3-(2-nitroethenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,4-dimethoxy-2-nitro-3-(2-nitroethenyl)-, (E)-(143814-63-5)
• EPA Substance Registry System: Benzene, 1,4-dimethoxy-2-nitro-3-(2-nitroethenyl)-, (E)-(143814-63-5)

Safety Data

• Hazardous Substances Data: 143814-63-5(Hazardous Substances Data)

Upstream product

• 75-52-5 nitromethane 
• 1206-55-9 3,6-dimethoxy-2-nitrobenzaldehyde 
• 93-02-7 2,5-dimethoxybenzaldehyde 

Downstream Products

• 845619-28-5 (1-benzenesulfonyl-4,7-dimethoxy-1H-indol-2-yl)-(pentafluorophenyl)-methanone 
• 845619-36-5 1-benzenesulfonyl-2-pentafluorobenzoyl-1H-indole-4,7-dione 
• 845619-27-4 (1-benzenesulfonyl-4,7-dimethoxy-1H-indol-2-yl)-(3,5-difluorophenyl)-methanone 
• 845619-35-4 1-benzenesulfonyl-2-(3,5-difluoro-benzoyl)-1H-indole-4,7-dione 
• 845619-22-9 (1-benzenesulfonyl-4,7-dimethoxy-1H-indol-2-yl)-morpholin-4-yl-methanone 
• 845619-25-2 (1-benzenesulfonyl-4,7-dimethoxy-1H-indol-2-yl)-(4-methoxyphenyl)-methanone 
• 845619-24-1 (1-benzenesulfonyl-4,7-dimethoxy-1H-indol-2-yl)-(3-methoxyphenyl)-methanone 
• 845619-30-9 1-benzenesulfonyl-2-(morpholine-4-carbonyl)-1H-indole-4,7-dione 
• 845619-26-3 (1-benzenesulfonyl-4,7-dimethoxy-1H-indol-2-yl)-(3-fluorophenyl)-methanone 
• 845619-32-1 1-benzenesulfonyl-2-(3-methoxy-benzoyl)-1H-indole-4,7-dione 
• 845619-33-2 1-benzenesulfonyl-2-(4-methoxy-benzoyl)-1H-indole-4,7-dione 
• 845619-34-3 1-benzenesulfonyl-2-(3-fluoro-benzoyl)-1H-indole-4,7-dione 
• 845619-23-0 (1-benzenesulfonyl-4,7-dimethoxy-1H-indol-2-yl)-phenyl-methanone 
• 845619-31-0 1-benzenesulfonyl-2-benzoyl-1H-indole-4,7-dione 

Relevant articles and documents

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Multistep synthesis (12 steps) of new pentacyclic compounds, which are structurally very close to natural marine alkaloids, was performed via a Diels-Alder reaction between 4-methylene-5-(bromomethylene)-4,5-dihydrothiazole and a protected dioxotryptamine

Synthesis and cytotoxic activity of 2-acyl-1H-indole-4,7-diones on human cancer cell lines

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AN IMPROVED SYNTHESIS OF 4,7-DIMETHOXY-1H-INDOLE

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