15515-54-5

Basic information

• Product Name: 2-methoxy-4,6-di-tert-butylphenol
• Synonyms: 2-methoxy-4,6-di-tert-butylphenol
• CAS NO: 15515-54-5
• Molecular Weight: 236.354
• Mol File: 15515-54-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-methoxy-4,6-di-tert-butylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-4,6-di-tert-butylphenol(15515-54-5)
• EPA Substance Registry System: 2-methoxy-4,6-di-tert-butylphenol(15515-54-5)

Safety Data

• Hazardous Substances Data: 15515-54-5(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 732-26-3 2,4,6-tri-tert-butylphenoxol 
• 1020-31-1 3,5-Di-tert-butylcatechol 
• 77-78-1 dimethyl sulfate 
• 90-05-1 2-methoxy-phenol 
• 75-65-0 tert-butyl alcohol 
• 115-11-7 isobutene 

Downstream Products

• 101777-28-0 4,6-di-tert-butyl-3-nitrobenzene-1,2-diol 
• 1020-31-1 3,5-Di-tert-butylcatechol 
• 4857-68-5 1-Methoxy-4,5-di-t-butyl-cyclohex-1-endi-3,6-on 
• 65077-00-1 1-Aethoxy-4,5-di-t-butyl-cyclohex-1-endi-3,6-on 
• 3383-21-9 3,5-di-tert-butyl-o-benzoquinone 
• 100699-37-4 2,4-di-t-butyl-4,6-dimethoxycyclohexa-2,5-dienone 
• 33974-40-2 2,4-Di-tert-butyl-6,6-dimethoxy-cyclohexa-2,4-dienone 
• 20039-94-5 2,4-di-tert-butyl-6-nitrophenol 

Relevant articles and documents

Transformations of organic molecules with F-TEDA-BF4 in ionic liquid media

The transformations of organic molecules with F-TEDA-BF4 (1) were investigated in the hydrophilic ionic liquid (IL) 1-butyl-3-methyl- imidazolium tetrafluoroborate ([bmim][BF4], 2) and the hydrophobic IL 1-butyl-3-methyl-imidazolium hexafluorophosphate ([bmim][PF6], 3). The range of substrates included alkyl substituted phenols 4a-c, 9, 13, 1,1-diphenylethene (15), alkyl aryl ketones 19-22, aldehydes 23-25 and methoxy-substituted benzene derivatives 26-30. The evaluation of the outcome of reactions performed in IL media in comparison to those of the corresponding reactions in conventional organic solvents revealed that the transformations in IL are less efficient and selective. The effect of the presence of a nucleophile (MeOH, H2O, MeCN) on the course of reaction was also studied.