22385-74-6

Basic information

• Product Name: 3,5-Di-tert-butyl-1,2-dimethoxybenzene
• Synonyms: 3,5-Di-tert-butyl-1,2-dimethoxybenzene
• CAS NO: 22385-74-6
• Molecular Weight: 250.381
• Mol File: 22385-74-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,5-Di-tert-butyl-1,2-dimethoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Di-tert-butyl-1,2-dimethoxybenzene(22385-74-6)
• EPA Substance Registry System: 3,5-Di-tert-butyl-1,2-dimethoxybenzene(22385-74-6)

Safety Data

• Hazardous Substances Data: 22385-74-6(Hazardous Substances Data)

Upstream product

• 91-16-7 1,2-dimethoxybenzene 
• 507-20-0 tertiary butyl chloride 
• 1020-31-1 3,5-Di-tert-butylcatechol 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 
• 120-80-9 benzene-1,2-diol 
• 75-65-0 tert-butyl alcohol 

Downstream Products

• 3383-21-9 3,5-di-tert-butyl-o-benzoquinone 

Relevant articles and documents

Reaction of aromatic radical cations with RuCl3·3H2O

Interactions of RuCl3·3H2O with radical cations of aromatic ethers, 1,4-di-tert-butyl-2,5-dimethoxybenzene, 3,5-di-tert-butyl-1,2-dimethoxybenzene and 2-tert-butyl-1,4-dimethoxybenzene, and with aromatic amines, 2,4,6-tri-tert-butylaniline and N,N,N′,N′-tetramethyl-1,4-phenylenediamine, were observed by voltammetry. ESR and UV spectroscopies were used for the study of the the first two ethers. The effect of RuCl3·3H2O was also examined by controlled potential electrolysis.

O-Methylation of tert-Alkylpyrocatecholes. Analytical Method for Determination of the Content of Product Mixtures and Way for Preparation of 4-tert-Alkylveratroles

The O-methylation of tert-alkylpyrocatecholes with dimethylsulfate leads to a mixture of substituted guaiacoles 6/7, 9/10 and veratroles 5, 6 which are separated by gas/liquid-chromatography for analytical purposes.It is also possible to prepare 4-tert-alkylsubstituted veratroles 5 with good yields in this way.On the other hand, the alkylation of veratrole was only successful with lower tert-alkanols or alkenes.Long-chained tert-alkanols fail in this reaction.The analytical and spectroscopical data of some new 4-tert-alkylveratroles 5a-g are given.