86475-21-0

Basic information

• Product Name: 2,3,4,5-tetramethoxyphenylformate
• Synonyms: 2,3,4,5-tetramethoxyphenylformate
• CAS NO: 86475-21-0
• Molecular Weight: 242.229
• Mol File: 86475-21-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,3,4,5-tetramethoxyphenylformate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,5-tetramethoxyphenylformate(86475-21-0)
• EPA Substance Registry System: 2,3,4,5-tetramethoxyphenylformate(86475-21-0)

Safety Data

• Hazardous Substances Data: 86475-21-0(Hazardous Substances Data)

Upstream product

• 2103-57-3 2,3,4-trimethoxybenzaldehyde 
• 30225-80-0 2,3,4-trimethoxyphenyl acetate 
• 30225-82-2 2,3,4-trimethoxyphenyl formate 
• 19676-64-3 2,3,4-trimethoxyphenol 
• 13909-73-4 2',3',4'-trimethoxyacetophenone 
• 21450-56-6 1,2,3,4-tetramethoxybenzene 
• 65884-12-0 2,3,4,5-tetramethoxybenzaldehyde 

Downstream Products

• 13909-75-6 1,2,3,4,5-pentamethoxybenzene 
• 86475-27-6 2,4-diamino-5-(2,3,4,5,6-pentamethoxybenzyl)pyrimidine 
• 86475-25-4 β-methoxy-α-(2,3,4,5,6-pentamethoxybenzylidene)propionitrile 
• 2174-59-6 5-hydroxy-6,7,8,3',4'-pentamethoxyflavone 
• 478-01-3 nobiletin 
• 654083-34-8 1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-3-(3,4-dimethoxyphenyl)-1,3-propanedione 
• 3162-28-5 2-hydroxy-3,4,5,6-tetramethoxyacetophenone 
• 30225-99-1 2,3,4,5-Tetramethoxyphenol 

Relevant articles and documents

Practical Synthesis of Polymethylated Flavones: Nobiletin and Its Desmethyl Derivatives

We present a practical synthesis of the polymethoxylated citrus flavone nobiletin that is suitable for use on a hundred gram scale. Ready availability of this compound and its derivatives will aid detailed chemical-biological investigations of their biological activities, including activation of signaling via the cAMP-dependent protein kinase A/extracellular signal-related protein kinase/cAMP response element-binding protein pathway.

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.