26532-80-9

Basic information

• Product Name: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(methylthio)-
• CAS NO: 26532-80-9
• Molecular Formula: C15H24OS
• Molecular Weight: 252.421
• Mol File: 26532-80-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(methylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(methylthio)-(26532-80-9)
• EPA Substance Registry System: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(methylthio)-(26532-80-9)

Safety Data

• Hazardous Substances Data: 26532-80-9(Hazardous Substances Data)

Upstream product

• 97496-00-9 C₁₅H₂₅OS 
• 489-01-0 2,6-Di-t-butyl-4-methoxyphenol 
• 3957-71-9 3,5-di-tert-butyl-4-hydroxyphenylthiocyanate 
• 128-39-2 2,6-di-tert-butylphenol 
• 950-59-4 4-hydroxy-3,5-di-tert-butylthiophenol 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 

Downstream Products

• 97496-00-9 C₁₅H₂₅OS 
• 489-01-0 2,6-Di-t-butyl-4-methoxyphenol 
• 94092-37-2 2,6-bis(1,1-dimethylethyl)-4-(methylsulfinyl)phenol 
• 97496-00-9 4-hydroxy-3,5-di-t-butylphenyl methyl sulphide radical 
• 84161-18-2 2,6-Di-tert-butyl-4-(methylsulfonyl)phenol 

Relevant articles and documents

Organochalcogen substituents in phenolic antioxidants

Little is known about the ED/EW character of organochalcogen substituents and their contribution to the O-H bond dissociation enthalpy (BDE) in phenolic compounds. A series of ortho- and para-(S,Se,Te)R-substituted phenols were prepared and investigated by EPR, IR, and computational methods. Substituents lowered the O-H BDE by >3 kcal/mol in the para position, while the ortho-effect was modest due to hydrogen bonding (～3 kcal/mol) to the O-H group.

Electronic and hydrogen bonding effects on the chain-breaking activity of sulfur-containing phenolic antioxidants

A kinetic and thermodynamic investigation of phenols para-substituted with thiyl (SR), sulfinyl (SOR), and sulfonyl (SO2R) groups and ortho-substituted with thiyl groups is reported. The effect of the sulfur substituents on the O-H bond dissoci

Phenolic thioethers as inhibitors of 5-lipoxygenase

The compounds of the present invention comprise substituted phenolic thioether derivatives that are specific inhibitors of 5-lipoxygenase and which, therefore, are useful in the treatment of local and systemic inflammation, allergy and hypersensitivity reactions and other disorders in which agents formed in the 5-lipoxygenase metabolic pathway are involved.