30225-99-1

Basic information

• Product Name: Phenol, 2,3,4,5-tetramethoxy-
• Synonyms: Phenol,2,3,4,5-tetramethoxy;3,4,5,6-Tetramethoxyphenol;2,3,4,5-Tetramethoxy-phenol
• CAS NO: 30225-99-1
• Molecular Formula: C10H14O5
• Molecular Weight: 214.218
• Mol File: 30225-99-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Phenol, 2,3,4,5-tetramethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2,3,4,5-tetramethoxy-(30225-99-1)
• EPA Substance Registry System: Phenol, 2,3,4,5-tetramethoxy-(30225-99-1)

Safety Data

• Hazardous Substances Data: 30225-99-1(Hazardous Substances Data)

Upstream product

• 634-36-6 1,2,3-trimethoxybenzene 
• 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 
• 2103-57-3 2,3,4-trimethoxybenzaldehyde 
• 30225-97-9 1-(2,3,4,5-tetramethoxyphenyl)ethan-1-one 
• 21450-56-6 1,2,3,4-tetramethoxybenzene 
• 30225-98-0 2,3,4,5-Tetramethoxy-acetoxybenzol 
• 86475-21-0 2,3,4,5-tetramethoxyphenylformate 
• 65884-12-0 2,3,4,5-tetramethoxybenzaldehyde 

Downstream Products

• 86475-25-4 β-methoxy-α-(2,3,4,5,6-pentamethoxybenzylidene)propionitrile 
• 128191-00-4 1-(2-Hydroxy-3,4,5,6-tetramethoxyphenyl)but-2-yn-1-one 
• 3117-05-3 2,3,5-trimethoxy-1,4-benzoquinone 
• 104202-51-9 2-Methoxymethyloxy-3,4,5,6-tetramethoxybenzaldehyde 
• 104202-47-3 3,4,5,6-Tetramethoxy-1-methoxymethyloxy-2-oxiranylbenzene 
• 478-01-3 nobiletin 
• 13909-75-6 1,2,3,4,5-pentamethoxybenzene 
• 128191-04-8 5,6,7,8-Tetramethoxy-2-<2-<3,5-bis(benzyloxy)phenyl>ethenyl>chromone 
• 103654-51-9 hormothamnione triacetate 
• 117970-66-8 2-hydroxy-3,4,5,6-tetramethoxy propiophenone 
• 117970-68-0 5,6,7,8-Tetramethoxy-2-<2-<3,5-bis(benzyloxy)phenyl>ethenyl>-3-methylchromone 
• 103654-49-5 Hormothamnione 
• 86475-27-6 2,4-diamino-5-(2,3,4,5,6-pentamethoxybenzyl)pyrimidine 
• 104202-38-2 1-methoxymethyloxy-2,3,4,5-tetramethoxybenzene 

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.

An Improved Synthesis of 1,4-Benzo- and 1,4-Naphthoquinones Bearing Active Substituents

The synthesis of 1,4-benzoquinones and 1,4-naphthoquinones 3a-j carrying substituents such as methoxyl, allyl or oxiranyl was substantially improved.The 1-methoxy-4-methoxymethyloxy 2a-d, g-k or 1,4-bis(methoxymethyloxy) derivatives 2e-f were used, as a substrates instead of 1,4-dimethoxy derivatives 1a-j hitherto used and they were oxidized with silver(II) dipicolinate.Among numerous examples, the synthesis of a new analog of ubiquinone 3d with the oxiranyl substituent, being a new bioactivated alkylating agent, is reported.