380305-91-9

Upstream product

• 380305-90-8 4-tert-butyl-2,6-bis-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-ylmethyl)-benzeneselenol 

Downstream Products

• 380305-97-5 C₆₀H₆₆S₂Se 
• 380305-90-8 4-tert-butyl-2,6-bis-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-ylmethyl)-benzeneselenol 
• 380305-94-2 C₆₀H₆₆SSe 

Relevant academic research and scientific papers

The first direct oxidative conversion of a selenol to a stable selenenic acid: Experimental demonstration of three processes included in the catalytic cycle of glutathione peroxidase

(matrix presented) A stable selenenic acid was synthesized by direct oxidation of a selenol bearing a novel bowl-type substituent with H2O2, and its structure was established by X-ray crystallographic analysis. Selenenyl sulfides obt