58045-92-4

Basic information

• Product Name: erythro-1-(3,4-dimethoxyphenyl)propane-1,2-diyl diacetate
• CAS NO: 58045-92-4
• Molecular Weight: 296.32
• Mol File: 58045-92-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: erythro-1-(3,4-dimethoxyphenyl)propane-1,2-diyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: erythro-1-(3,4-dimethoxyphenyl)propane-1,2-diyl diacetate(58045-92-4)
• EPA Substance Registry System: erythro-1-(3,4-dimethoxyphenyl)propane-1,2-diyl diacetate(58045-92-4)

Safety Data

• Hazardous Substances Data: 58045-92-4(Hazardous Substances Data)

Upstream product

• 20133-19-1 1',2'-Dihydroxymethylisoeugenol 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 6379-72-2 1,2-dimethoxy-4-(E)-propenylbenzene 
• 64-19-7 acetic acid 
• 5912-87-8 (E)-1-(4-acetoxy-3-methoxyphenyl)-1-propene 

Relevant articles and documents

Electron-transfer Processes: Oxidation of α- and β-Alkenylbenzenes by Peroxydisulphate in Acetic Acid

Oxidation of α- and β-unsaturated alkylbenzenes by peroxydisulphate in acetic acid gives side-chain acetoxylation with formation of the corresponding glycol diacetates and compounds (10), respectively.The reaction is catalysed by transition-metal salts, among which cupric acetate gives the best results.Generally, electron-releasing substituents on the benzene ring increase the yield and improve the selectivity.The same substrates are oxidized in water under Ag+ catalysis to the corresponding aldehydes.The different behaviour in the two solvents is ascribed to the difference in reactivity between the primary oxidation products and the starting olefin, whereas the initial oxidation step is suggested to occur in both cases via an electron-transfer process from the olefin to the sulphate radical anion.