55386-54-4

Upstream product

• 72023-44-0 2,3,4,5-tetramethoxybenzoic acid 
• 118-41-2 Eudesmic acid 
• 23346-82-9 2-bromo-3,4,5-trimethoxybenzoic acid 

Downstream Products

• 141082-03-3 N-((S)-1-Hydroxymethyl-2-methyl-propyl)-2,3,4,5-tetramethoxy-benzamide 
• 109745-55-3 2,3,4,5-tetramethoxybenzamide 
• 141082-08-8 (R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 6'-hydroxy-4,5,6,2',3',4'-hexamethoxy-biphenyl-2-yl ester 
• 141082-01-1 (S)-4-tert-Butyl-2-(2,3,4,5-tetramethoxy-phenyl)-4,5-dihydro-oxazole 
• 109745-63-3 2-{2-[6-(1-Allyloxy-ethyl)-benzo[1,3]dioxol-5-yl]-3,4,5-trimethoxy-benzyl}-malonic acid dimethyl ester 
• 109745-64-4 2-{2-[6-(1-Hydroxy-ethyl)-benzo[1,3]dioxol-5-yl]-3,4,5-trimethoxy-benzyl}-malonic acid dimethyl ester 
• 109745-62-2 5-(1-Allyloxy-ethyl)-6-(6-bromomethyl-2,3,4-trimethoxy-phenyl)-benzo[1,3]dioxole 
• 109745-61-1 {2-[6-(1-Allyloxy-ethyl)-benzo[1,3]dioxol-5-yl]-3,4,5-trimethoxy-phenyl}-methanol 
• 73252-70-7 dimethyl 2-<1'-(2'-bromoacetyl-4',5'-methylenedioxyphenyl)>-3,4,5-trimethoxybenzylmalonate 
• 73252-69-4 dimethyl 2-<1'-(2'-acetyl-4',5'-methylenedioxyphenyl)>-3,4,5-trimethoxybenzylmalonate 
• 141082-05-5 (S)-4-Isopropyl-2-(2,3,4,5-tetramethoxy-phenyl)-4,5-dihydro-oxazole 
• 29620-05-1 methyl 2,3,4,5-tetramethoxybenzoate 

Relevant academic research and scientific papers

Is 2,3,4,5-tetramethoxybenzoyl chloride a natural product?

The title compound, which was reported to be a constituent of the fruiting body of the fungus Antrodia camphorata, has been synthesized. The reactivity and spectroscopic properties of the synthetic material do not match those of the natural product. There

Chiral oxazoline route to enantiomerically pure biphenyls: Magnesio and copper mediated asymmetric hetero- and homo-coupling reactions

A series of chiral biphenyls were prepared via asymmetric reactions involving chiral oxazolines. One series of chiral biphenyls was reached by the magnesium mediated coupling of aryl bromides (via their Grignard reagents) with o-methoxyaryl oxazolines. In

A highly stereoselective synthesis of axially chiral biaryls. Application to the synthesis of a potential chiral catalyst

Excellent diastereoselectivities (>98.2) have been obtained in the biaryl coupling of 2',6',-disubstituted aryl Grignard reagents 1 with aryl oxazolines 6, conveniently synthesised from the optically pure amino alcohols L-valinol and (S)-t-leucinol.