75467-59-3

Basic information

• Product Name: 3,5-di-tert-butyl-3',5'-dimethoxy-4,4'-biphenol
• Synonyms: 3,5-di-tert-butyl-3',5'-dimethoxy-4,4'-biphenol
• CAS NO: 75467-59-3
• Molecular Weight: 358.478
• Mol File: 75467-59-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,5-di-tert-butyl-3',5'-dimethoxy-4,4'-biphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-di-tert-butyl-3',5'-dimethoxy-4,4'-biphenol(75467-59-3)
• EPA Substance Registry System: 3,5-di-tert-butyl-3',5'-dimethoxy-4,4'-biphenol(75467-59-3)

Safety Data

• Hazardous Substances Data: 75467-59-3(Hazardous Substances Data)

Upstream product

• 950-57-2 4-bromo-2,6-di-tert-butylcyclohexa-2,5-dienone 
• 91-10-1 1,3-dimethoxy-2-hydroxy-benzene 
• 28096-16-4 2,6-di-tert-butyl-4-propionylphenoxy radical 
• 128-39-2 2,6-di-tert-butylphenol 

Relevant articles and documents

Silver ion-mediated coupling of 4-bromo-2,6-di-tert-butylcycohexa-2,5- dienone with phenols

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Oxidation of 2,6-Dimethoxyphenol with 2,6-Di-tert-butyl-4-propionylphenoxy Radical. Evidence for the Formation of an Intermediate "Radical Pair"

In the title reaction an intermediate is formed which is stable at temperatures below -10 deg C.It gives no EPR signal.Warming leads to the formation of coerulignone and poly-2,6-dimethoxyphenylene oxide.Acid hydrolysis at low temperatures leads to cross-coupled products.The results are discussed in terms of a two-stage reaction mechanism for the formation of a bond between two phenoxy radicals.