55386-54-4

Basic information

• Product Name: 2,3,4,5-Tetramethoxybenzoylchlorid
• Synonyms: 2,3,4,5-Tetramethoxybenzoylchlorid
• CAS NO: 55386-54-4
• Molecular Weight: 260.674
• Mol File: 55386-54-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,3,4,5-Tetramethoxybenzoylchlorid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,5-Tetramethoxybenzoylchlorid(55386-54-4)
• EPA Substance Registry System: 2,3,4,5-Tetramethoxybenzoylchlorid(55386-54-4)

Safety Data

• Hazardous Substances Data: 55386-54-4(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 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 
• 109745-55-3 2,3,4,5-tetramethoxybenzamide 
• 141082-03-3 N-((S)-1-Hydroxymethyl-2-methyl-propyl)-2,3,4,5-tetramethoxy-benzamide 

Relevant articles and documents

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

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.