264147-43-5

Upstream product

• 67-56-1 methanol 
• 125438-30-4 3-(2,4,5-trimethoxyphenyl)propionic acid 
• 824950-88-1 3-(2,4-dihydroxy-5-methoxy-phenyl)-propionic acid 
• 106128-88-5 2,4,5-trimethoxy cinnamaldehyde 
• 5273-86-9 C₁₂H₁₆O₃ 
• 80749-75-3 (E)-3-(2,4,5-trimethoxy-phenyl)-acrylic acid methyl ester 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 292638-85-8 acrylic acid methyl ester 
• 352279-44-8 methyl 2,4,5-trimethoxycinnamate 

Downstream Products

• 857777-54-9 (2,4,5-trimethoxy-phenethyl)-carbamic acid ethyl ester 
• 15394-83-9 1-(2,4,5-trimethoxyphenyl)-2-aminoethane 
• 125438-29-1 3-(2,4,5-trimethoxy-phenyl)-propionic acid amide 

Relevant academic research and scientific papers

A short and facile synthesis of 2-(1Z)-(3-hydroxy-3,7-dimethylocta-1,6- dienyl)-1,4-benzenediol and 1-(3′-methoxypropanoyl)-2,4,5- trimethoxybenzene isolated from Cordia alliodora

A novel synthesis of 2-(1Z)-(3-hydroxy-3,7-dimethylocta-1,6-dienyl)-1,4- benzenediol and 1-(3′-methoxypropanoyl)-2,4,5-trimethoxybenzene has been carried out by making use of an easily available starting material, acceleration by MW irradiation and the use of water as a green solvent in the key steps.

Solid-supported green synthesis of substituted hydrocinnamic esters by focused microwave irradiation

An efficient chemoselective hydrogenation protocol for substituted cinnamic esters is developed for the synthesis in quantitative yield of corresponding bioactive dihydrocinnamic esters with solid-supported palladium chloride/ammonium formate (cat.) in HCOOH/H2O 1:2 as a hydrogenating agent under focused-microwave irradiation for 10 min.

Friedel-crafts reaction of activated benzene rings with captodative and electron-deficient alkenes. A one-step synthesis of the natural product methyl 3-(2,4,5-trimethoxyphenyl)propionate

Electrophilic aromatic substitution of activated benzenes with the captodative olefin 1-acetylvinyl-1-p-nitrobenzoate (9), and with the electron-deficient alkenes methyl acrylate (8a), methylvinylketone (8b), and acrolein (8c) were evaluated under Lewis a

A concise conversion of β-asarone into 1-(3′- methoxypropanoyl)-2,4,5-trimethoxybenzene occurring in Cordia alliodora

The first synthesis of 1-(3′-methoxypropanoyl)-2,4,5- trimethoxybenzene 4, a natural phenylpropanoid occurring in Cordia alliodora, has been achieved, from β-asarone 1 of Acorus calamus. Selenium dioxide oxidation of 1 leads to 2,4,5-trimethoxycinnamaldeh