32176-96-8

Usage

Chemical compound

Benzenemethanol, 2,5-dimethoxy-4-methyl-

Upstream product

• 4925-88-6 2,5-dimethoxy-4-methylbenzaldehyde 
• 95-71-6 2-methylbenzene-1,4-diol 
• 246543-82-8 2-(2,5-dimethoxy-4-methyl-phenyl)-[1,3]dioxolane 
• 24599-58-4 2,5-dimethoxy toluene 
• 939019-26-8 2,5-dihydroxy-4-methyl-benzyl alcohol 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 38439-84-8 2,5-Dimethoxy-4-methylbenzyl phenylcarbonat 
• 32183-52-1 Acetic acid 2,5-dimethoxy-4-methyl-benzyl ester 
• 32185-60-7 4-Acetoxymethyltoluchinon 
• 38439-88-2 Dimethyl-carbamic acid 2,5-dimethoxy-4-methyl-benzyl ester 
• 38439-87-1 Methyl-carbamic acid 2,5-dimethoxy-4-methyl-benzyl ester 
• 38439-86-0 Carbamic acid 2,5-dimethoxy-4-methyl-benzyl ester 
• 38439-91-7 2-Methyl-5-(N-methyl-N-nitroso-carbamoyloxymethyl)-p-benzochinon 
• 38439-90-6 2-(N,N-Dimethylcarbamoyloxymethyl)-5-methyl-p-benzochinon 
• 38439-89-3 2-Hydroxymethyl-5-methyl-1,4-benzochinon-carbamat 
• 4925-88-6 2,5-dimethoxy-4-methylbenzaldehyde 
• 32378-21-5 2-(Chloromethyl)-5-methyl-1,4-dimethoxybenzene 
• 32176-94-6 4-methyl-2,5-dimethoxy-benzoic acid 
• 127870-62-6 2-[2-(2,5-Dimethoxy-4-methyl-benzyl)-3-methoxy-phenyl]-4,4-dimethyl-4,5-dihydro-oxazole 
• 51837-74-2 2-(2',5'-dimethoxy-4'-methylbenzyl)-3-methoxybenzoic acid 

Relevant academic research and scientific papers

Synthesis of quinones from hydroquinone dimethyl ethers. Oxidative demethylation with cobalt(III) fluoride

The oxidative demethylation of 1,4-dimethoxynaphthalene and 1,4- dimethoxybenzene derivatives with cobalt(III) fluoride proceeded in good to excellent yield to afford the corresponding naphthoquinone and benzoquinone derivatives.

A New Synthesis of Anthraquinones Using Dihydro-oxazoles and Grignard Reagents Derived from Mg(Anthracene)(THF)3

A general synthesis of anthraquinones which depends on the displacement of the methoxy group from an o-methoxyaryldihydro-oxazole by a methoxy substituted benzylmagnesium chloride, generated by using a magnesium-anthracene complex, has been developed.The masked benzylbenzoic acids which result from these reactions are deprotected and then ring-closed to anthrones which on oxidation yield anthraquinones.In this way, the followeing naturally occurring anthraquinones (or derivatives thereof have been synthesized): chrysophanol (9), islandicin (19), digitopurpone (21), tri-O-methylemodin (26), and di-O-methylsoranjidiol (29).