53135-85-6Relevant academic research and scientific papers
SYNTHESIS OF SOME THIOMETHYL DERIVATIVES OF 2,6-DI-tert-BUTYLPHENOL AND THEIR ANTIOXIDANT CHARACTERISTICS
Bilalov, S. B.,Alieva, F. D.,Gasanov, B. R.
, p. 1355 - 1357 (2007/10/02)
The reactions of 3,5-di-tert-butyl-4-hydroxybenzyl-N-N-dimethylamine with various thiols leads to the formation of 3,5-di-tert-butyl-4-hydoxybenzyl alkyl (aryl) sulfides.By means of their electrochemical oxidation at a stationary graphite microelectrode in aqueous media over a wide range of pH it was established that the new sulfides have the same level of antiradical activity as ionole. 3,5-Ditert-butyl-4-hydroxybenzyl sulfide is the most easily oxidized.
