1705-94-8

Basic information

• Product Name: acetic acid 10-oxo-9,10-dihydro-anthracen-9-yl ester
• Synonyms: acetic acid 10-oxo-9,10-dihydro-anthracen-9-yl ester
• CAS NO: 1705-94-8
• Molecular Weight: 252.269
• Mol File: 1705-94-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: acetic acid 10-oxo-9,10-dihydro-anthracen-9-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: acetic acid 10-oxo-9,10-dihydro-anthracen-9-yl ester(1705-94-8)
• EPA Substance Registry System: acetic acid 10-oxo-9,10-dihydro-anthracen-9-yl ester(1705-94-8)

Safety Data

• Hazardous Substances Data: 1705-94-8(Hazardous Substances Data)

Upstream product

• 613-31-0 9,10-dihydroanthracene 
• 64-19-7 acetic acid 
• 642-31-9 9-anthracene aldehyde 

Downstream Products

• 84-65-1 9,10-phenanthrenequinone 
• 4981-66-2 9,10-Dihydroxyanthracene 
• 1499-10-1 9,10-diphenylanthracene 
• 781-43-1 9,10-dimethylanthracene 

Relevant articles and documents

Oxidative aromatization of 4,7-dihydro-6-nitroazolo[1,5-a] pyrimidines: Synthetic possibilities and limitations, mechanism of destruction, and the theoretical and experimental substantiation

The reaction tolerance of the multicomponent process between 3-aminoazoles, 1-morpholino2-nitroalkenes, and aldehydes was studied. The main patterns of this reaction have been established. Conditions for the oxidation of 4,7-dihydro-6-nitroazolo[1,5-a]pyrimidines were selected. Previous claims that the 4,7-dihydro-6-nitroazolo[1,5-a]pyrimidines could not be aromatised have now been refuted. Compounds with an electron-donor substituent at position seven undergo decomposition during oxidation. The phenomenon was explained based on experimental data, electro-chemical experiment, and quantum-chemical calculation. The mechanism of oxidative degradation has been proposed.