135979-40-7

Upstream product

• 117-80-6 2,3-Dichloro-1,4-naphthoquinone 
• 128-39-2 2,6-di-tert-butylphenol 

Downstream Products

• 135979-39-4 2-(3,5-Di-tert-butyl-4-hydroxyphenyl)-3-(N-methylpiperazin-1-yl)-1,4-naphthochinon 
• 135979-36-1 2-(3,5-Di-tert-butyl-4-hydroxyphenyl)-3-methoxy-1,4-naphthochinon 
• 135979-37-2 2-(3,5-di-tert-butyl-4-hydroxyphenyl)-3-hydroxy-1,4-naphthoquinone 
• 198348-39-9 2-(3-tert-Butyl-4-hydroxyphenyl)-3-chlor-1,4-naphthochinon 
• 135979-38-3 2-(3,5-Di-tert-butyl-2,5-cyclohexadien-4-on-1-yliden)-1,2,3,4-tetrahydronaphthalin-1,3,4-trion 
• 717879-62-4 Ethyl-5-(3,5-di-tert-butyl-4-hydroxyphenyl)-6-hydroxy-3H-naphtho[2,1-b][1,4]thiazin-2-carboxylat 

Relevant academic research and scientific papers

Influence of 2-aryl-3-halogen/3-hydroxy-1,4-naphthoquinones with salicylic and cinnamic acid partial structures on the arachidonic acid cascade

Searching for more potent 5-lipoxygenase (LO) inhibitors one tert-butyl group of the selective 5-LO-inhibitor 2-(3,5-di-tert-butyl-4-hydroxyphenyl)-3-hydroxy-1,4-naphthoquinone (1) was substituted by polar functions (-CHO, -COOH, -CH=CH-COOR, -CH 2/

NUCLEOPHILIC ARYLATION OF DERIVATIVES OF NAPHTHO- AND ANTHRAQUINONES WITH 2,6-DI-tert-BUTYLPHENOL

Derivatives of naphtho- and anthraquinones are arylated by sterically hindered 2,6-di-tert-butylphenol in DMSO with the addition of potassium carbonate or potassium hydroxide.The reaction takes place selectively at the para-carbon atom of the phenol, and the corresponding 3,5-di-tert-butyl-4-hydroxyphenyl derivatives of 1,4-naphthol- and 9,10-anthraquinones are formed.