5600-82-8

Usage

Chemical class

Methoxyphenols

Structure

Derivative of phenol with two methoxy groups and a methyl group attached to the benzene ring

Uses

Chemical synthesis, research, potential medical applications in drug development

Safety

Handle with care, follow necessary safety precautions due to potential hazards

Upstream product

• 100940-11-2 2,5-dimethoxy-3-methylbenzoic acid 
• 5548-30-1 2,5-dimethoxy-3-methylbenzaldehyde 
• 127870-68-2 2,5-dimethoxy-3-methylbenzonitrile 
• 5307-05-1 1-hydroxy-4-methoxy-2-methylbenzene 
• 13523-12-1 1-bromo-2,5-dimethoxy-3-methylbenzene 
• 5600-81-7 2-Hydroxy-5-methoxy-3-methylbenzylalkohol 
• 74-88-4 methyl iodide 

Downstream Products

• 76-84-6 triphenylmethyl alcohol 
• 88208-72-4 2,5-dimethoxy-3-methylbenzyl triphenylmethyl ether 
• 88208-76-8 2-bromo-3,6-dimethoxy-5-methylbenzyl alcohol 
• 88208-75-7 4-bromo-2,5-dimethoxy-3-methylbenzyl alcohol 
• 88208-73-5 4-bromo-2,5-dimethoxy-3-methylbenzyl triphenylmethyl ether 
• 88208-74-6 6-bromo-2,5-dimethoxy-3-methylbenzyl triphenylmethyl ether 
• 127870-63-7 4,5-dihydro-2-<2-(2',5'-dimethoxy-3'-methylbenzyl)-2-methoxyphenyl>-4,4-dimethyloxazole 
• 127870-64-8 2-(2',5'-dimethoxy-3'-methylbenzyl)-3-methoxybenzoic acid 
• 88208-80-4 (E)-4-bromo-2,2',5,6'-tetramethoxy-3-methylstilbene 
• 88208-80-4 (Z)-4-bromo-2,2',5,6'-tetramethoxy-3-methylstilbene 
• 88208-78-0 4-bromo-2,5-dimethoxy-3-methylbenzyltriphenylphosphonium bromide 
• 88208-81-5 (E)-methyl 2,2',5,6'-tetramethoxy-3-methylstilbene-4-carboxylate 
• 88208-82-6 (E)-2,2',5,6'-tetramethoxy-3-methylstilbene-4-carboxylic acid 
• 88208-77-9 4-bromo-2,5-dimethoxy-3-methylbenzyl bromide 

Relevant academic research and scientific papers

Radical reactions leading to substituted coumarins

The reaction of 4-hydroxycoumarins with a series of quinonic chlorides under photostimulation was shown to provide an efficient approach to 3- alkylated coumarin derivatives. Alkylation reactions of this type proceeded via an electron transfer mechanism (

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).