56002-80-3

Basic information

• Product Name: 2-acetoxy-1,3,4,5-tetramethoxybenzene
• Synonyms: 2-acetoxy-1,3,4,5-tetramethoxybenzene
• CAS NO: 56002-80-3
• Molecular Weight: 256.255
• Mol File: 56002-80-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-acetoxy-1,3,4,5-tetramethoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-acetoxy-1,3,4,5-tetramethoxybenzene(56002-80-3)
• EPA Substance Registry System: 2-acetoxy-1,3,4,5-tetramethoxybenzene(56002-80-3)

Safety Data

• Hazardous Substances Data: 56002-80-3(Hazardous Substances Data)

Upstream product

• 7508-05-6 1-(2,3,4,6-tetramethoxyphenyl)ethanone 
• 7507-98-4 1-(2-hydroxy-3,4,6-trimethoxyphenyl)ethanone 
• 5333-45-9 1,2,3,5-tetramethoxybenzene 

Downstream Products

• 13909-75-6 1,2,3,4,5-pentamethoxybenzene 
• 3162-28-5 2-hydroxy-3,4,5,6-tetramethoxyacetophenone 
• 654083-34-8 1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-3-(3,4-dimethoxyphenyl)-1,3-propanedione 
• 478-01-3 nobiletin 
• 2174-59-6 5-hydroxy-6,7,8,3',4'-pentamethoxyflavone 
• 53887-77-7 2-hydroxy-3,4,5,6-tetramethoxybenzene 

Relevant articles and documents

PET imaging of nobiletin based on a practical total synthesis

A practical synthesis of nobiletin, a polymethoxylated citrus flavone, was accomplished by utilizing our novel flavone synthesis. Synthetic nobiletin was labelled by selective demethylation and rapid incorporation of 11C atom. Positron emission tomography images successfully visualized the brain distribution, which may provide therapeutic benefits in the treatment of Alzheimer's disease. The Royal Society of Chemistry.

The Baeyer-Villiger Oxidation of Aromatic Aldehydes and Ketones with Hydrogen Peroxide Catalyzed by Selenium Compounds

A series of organoselenium compounds was investigated as activators of hydrogen peroxide in the Baeyer-Villiger oxidation.As a result, a convenient and cheap method for transformation of aromatic aldehydes, having polycondensed ring systems or electron-donating substituents, and polymethoxy derivatives of acetophenone, into phenols was elaborated.This method utilizes hydrogen peroxide activated by areneseleninic acids, as oxidizing agent.