104202-38-2

Upstream product

• 30225-99-1 2,3,4,5-Tetramethoxyphenol 
• 107-30-2 chloromethyl methyl ether 
• 65884-12-0 2,3,4,5-tetramethoxybenzaldehyde 
• 21450-56-6 1,2,3,4-tetramethoxybenzene 

Downstream Products

• 111023-31-5 2-Methyl-1-(2,3,4,5-tetramethoxy-6-methoxymethoxy-phenyl)-propan-1-one 
• 3117-05-3 2,3,5-trimethoxy-1,4-benzoquinone 
• 104202-51-9 2-Methoxymethyloxy-3,4,5,6-tetramethoxybenzaldehyde 
• 104202-47-3 3,4,5,6-Tetramethoxy-1-methoxymethyloxy-2-oxiranylbenzene 
• 111023-44-0 2-Isobutyryl-3,5,6-trimethoxy-[1,4]benzoquinone 

Relevant academic research and scientific papers

Ouinone derivatives and pharmacological use

A quinone derivative useful in the treatment of hepatic diseases defined by the general formula: STR1 where R1 is selected from the group consisting of alkyl, alkenly, alkynyl or heterocycle, R2 is a substituted nitrogen containing radical wherein the sub

An Improved Synthesis of 1,4-Benzo- and 1,4-Naphthoquinones Bearing Active Substituents

The synthesis of 1,4-benzoquinones and 1,4-naphthoquinones 3a-j carrying substituents such as methoxyl, allyl or oxiranyl was substantially improved.The 1-methoxy-4-methoxymethyloxy 2a-d, g-k or 1,4-bis(methoxymethyloxy) derivatives 2e-f were used, as a substrates instead of 1,4-dimethoxy derivatives 1a-j hitherto used and they were oxidized with silver(II) dipicolinate.Among numerous examples, the synthesis of a new analog of ubiquinone 3d with the oxiranyl substituent, being a new bioactivated alkylating agent, is reported.