17258-83-2

Upstream product

• 2091-51-2 4-(bromomethyl)-2,6-di-tert-butylphenol 
• 3699-30-7 potassium diethyldithiocarbamate 
• 75-15-0 carbon disulfide 
• 50-00-0 formaldehyd 
• 128-39-2 2,6-di-tert-butylphenol 
• 109-89-7 diethylamine 
• 88-27-7 N,N-dimethyl-(3,5-di-tert-butyl-4-hydroxybenzyl)amine 

Downstream Products

• 30184-00-0 2-(3,5-Di-tert-butyl-4-hydroxy-benzyl)-3-(3,5-di-tert-butyl-4-hydroxy-phenyl)-2-(diethoxy-phosphoryl)-propionic acid ethyl ester 
• 60309-99-1 2,2-Bis-(3,5-di-tert-butyl-4-hydroxy-benzyl)-malonamide 
• 23613-17-4 2,2-Bis-(3,5-di-tert-butyl-4-hydroxy-benzyl)-malonic acid dioctadecyl ester 
• 60310-00-1 2-Benzenesulfonyl-2-(3,5-di-tert-butyl-4-hydroxy-benzyl)-3-(3,5-di-tert-butyl-4-hydroxy-phenyl)-propionamide 
• 60309-98-0 2,2-Bis-(3,5-di-tert-butyl-4-hydroxy-benzyl)-malonic acid bis-(4-sec-butyl-phenyl) ester 
• 60310-01-2 2-Benzenesulfonyl-2-(3,5-di-tert-butyl-4-hydroxy-benzyl)-3-(3,5-di-tert-butyl-4-hydroxy-phenyl)-propionitrile 
• 5082-72-4 1-[3,5-di-tert-butyl-4-hydroxyphenyl]-butan-3-one 
• 39266-71-2 2,2-Bis-(3,5-di-tert-butyl-4-hydroxy-benzyl)-malononitrile 
• 39617-24-8 2-Cyano-2-(3,5-di-tert-butyl-4-hydroxy-benzyl)-3-(3,5-di-tert-butyl-4-hydroxy-phenyl)-propionic acid methyl ester 
• 51511-18-3 3,5-di-t-butyl-4-hydroxybenzylmalonic acid,dimethyl ester 
• 39266-67-6 dimethyl bis(3,5-di-tert-butyl-4-hydroxybenzyl)malonate 
• 56856-09-8 methyl-[1-(3,5-ditert.butyl-4-hydroxybenzyl)-n-butyl]-ketone 
• 35965-68-5 2-(3,5-ditert-butyl-4-hydroxybenzyl)-cyclohexanone 

Relevant academic research and scientific papers

Acetyl chloride - 3,5-di(tert-butyl)-4-hydroxy-N,N-dimethylbenzylamine salt in the benzylation of organic and inorganic sulfur-containing compounds

The reactions of the quaternary acylammonium salt formed on treatment of 3,5-di-tert-butyl-4-hydroxy-N,N-dimethylbenzylamine with acetyl chloride, with various organic and inorganic sulfur-containing compounds were studied.The possibility of using this salt for the introduction of a sterically hindered phenol moiety in various sulfur-containing compounds was shown. - Key words: sterically hindered phenols, quaternary ammonium salts, benzylation, thiourea.