94092-37-2

Upstream product

• 64741-01-1 m-chloroperoxybenzoic acid 
• 26532-80-9 2,6-di-tert-butyl-4-(methylsulfanyl)phenol 
• 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 

Downstream Products

• 97499-03-1 C₁₅H₂₃O₂S 
• 84161-18-2 2,6-Di-tert-butyl-4-(methylsulfonyl)phenol 

Relevant academic research and scientific papers

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.

Phenolic thioethers as inhbitors 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.