876389-30-9

Upstream product

• 876389-35-4 2-bromo-5-methoxy-3,4,6-trimethylbenzyl chloride 
• 51857-41-1 4-bromo-2,3,6-trimethylphenol 
• 876389-28-5 4-bromo-2,3,6-trimethylanisole 
• 876389-29-6 tert-butyl 2-(2-bromo-5-methoxy-3,4,6-trimethylbenzyl)acetoacetate 
• 2416-94-6 2,3,6-trimethylphenol 

Downstream Products

• 876389-31-0 2-[2-(2-bromo-5-methoxy-3,4,6-trimethylphenyl)ethyl]-2-methyl-1,3-dioxolane 
• 876389-23-0 1-(2-benzylselenenyl-5-methoxy-3,4,6-trimethylphenyl)-3,7,11,15-tetramethyl-3-hexadecanol 
• 876389-32-1 2-[2-(2-benzylselenenyl-5-methoxy-3,4,6-trimethylphenyl)ethyl]-2-methyl-1,3-dioxolane 
• 876389-33-2 2-(2-benzylselenenyl-5-methoxy-3,4,6-trimethylphenyl)ethyl methyl ketone 

Relevant academic research and scientific papers

Synthesis and antioxidant profile of all-rac-α-selenotocopherol

all-rac-α-Selenotocopherol (6c) has been synthesized in 11 steps in 6.6% total yield. Key steps include chloromethylation to approach the persubstituted aromatic 9b and cyclization of alcohol precursor 10 by radical homolytic substitution at selenium to f