60241-75-0

Upstream product

• 60241-74-9 2,3,6-trimethoxybenzoic acid 
• 77-78-1 dimethyl sulfate 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 79-22-1 methyl chloroformate 
• 67-56-1 methanol 

Downstream Products

• 60241-74-9 2,3,6-trimethoxybenzoic acid 
• 79817-85-9 2-Hydroxy-3,5,6-tribrom-1,4-benzochinon 
• 60241-76-1 3-(1-methyl-1-hydroxyethyl)-1,2,4-trimethoxybenzene 
• 866464-91-7 4-(1-methylethyl)-2,3,5-trimethoxybenzaldehyde 
• 866464-96-2 4-isopropyl-2,3,5-trimethoxybenzyl chloride 
• 60241-78-3 3-(1-methylethyl)-1,2,4-trimethoxybenzene 
• 60241-77-2 1,2,4-trimethoxy-3-(prop-1-en-2-yl)benzene 
• 156723-06-7 4-(1-methylethyl)-2,3,5-trimethoxyphenylmethyl alcohol 
• 25991-81-5 1,3-dihydroxy-7,8-dimethoxyxanthone 
• 114567-42-9 1,3-dihydroxy-5,8-dimethoxyxanthone 

Relevant academic research and scientific papers

Method for preparing 1,3,5,8-tetrahydroxy xanthone and 1,3,7,8-tetrahydroxy xanthone

The invention discloses a method for preparing 1,3,5,8-tetrahydroxy xanthone and 1,3,7,8-tetrahydroxy xanthone. The method comprises the following steps: by taking 1,2,4-trimetoxybenzene as an initialraw material, and adding n-butyllithium and a chloro-ca

Synthesis of 1,2,4-trimethoxybenzene and its selective functionalization at C-3 by directed metalation

A new and efficient strategy was developed for the preparation of 1,2,4-trimethoxybenzene (3, a powerful attractant of Euglossini bees) and its C-3 derivatives (7a-j), from vanillin (2) in 56% overall yield.

Stereoselective syntheses of (±)-komaroviquinone and (±)-faveline methyl ether through intramolecular Heck reaction

An efficient, flexible, and stereoselective convergent route for constructing the trans-10-hydroxy-1,1-dimethyloctahydrodibenzo[a,d]cyclohepten- 7-ones (5a-c) was achieved via intramolecular Heck reaction. This strategy has been successfully implemented for the syntheses of (±)-komaroviquinone (3) through (±)-coulterone dimethyl ether (5c) and (±)-faveline methyl ether (1a).