218444-39-4

Basic information

• Product Name: 2-[[3,5-dimethoxy-4-(3-methyl-2-butenyl)]phenyl]-6-(tert-butyldimethylsilanyloxy)benzofuran
• Synonyms: 2-[[3,5-dimethoxy-4-(3-methyl-2-butenyl)]phenyl]-6-(tert-butyldimethylsilanyloxy)benzofuran
• CAS NO: 218444-39-4
• Molecular Weight: 452.666
• Mol File: 218444-39-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-[[3,5-dimethoxy-4-(3-methyl-2-butenyl)]phenyl]-6-(tert-butyldimethylsilanyloxy)benzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[[3,5-dimethoxy-4-(3-methyl-2-butenyl)]phenyl]-6-(tert-butyldimethylsilanyloxy)benzofuran(218444-39-4)
• EPA Substance Registry System: 2-[[3,5-dimethoxy-4-(3-methyl-2-butenyl)]phenyl]-6-(tert-butyldimethylsilanyloxy)benzofuran(218444-39-4)

Safety Data

• Hazardous Substances Data: 218444-39-4(Hazardous Substances Data)

Upstream product

• 870-63-3 prenyl bromide 
• 218444-38-3 2-(3,5-dimethoxyphenyl)-6-(tert-butyl-dimethylsilanyloxy)benzofuran 
• 41777-08-6 2,4-diacetoxybenzaldehyde 
• 6272-26-0 6-hydroxybenzofuran-3-one 
• 299912-77-9 6-(tert-butyl-dimethylsilanyloxy)-[2H]-benzofuran-3-one 
• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 218444-32-7 2,4-Bis(3',5'-dimethoxybenzoyloxy)benzyl alcohol 
• 218444-31-6 2,4-Bis(3',5'-dimethoxybenzoyloxy)benzaldehyde 
• 218444-34-9 6-(3'',5''-Dimethoxybenzoyloxy)-2-(3',5'-dimethoxyphenyl)benzo[b]furan 
• 218444-37-2 6-Acetoxy-2-(3',5'-dimethoxyphenyl)benzo[b]furan 
• 218444-35-0 5-acetoxy-2-acetoxymethylphenol 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 134937-20-5 2-(3,5-dimethoxyphenyl)-6-hydroxybenzofuran 

Relevant articles and documents

Total synthesis of the 2-arylbenzo[b]furan-containing natural products from Artocarpus

In this study, 2-arylbenzo[b]furan-containing derivatives moracin C (1) and moracin M (4), the natural products from Artocarpus, have been synthesized in highest overall yield to date (1, 7 steps with an overall yield of 41.9%; 4, 6 steps with an overall yield of 56.3%), and we also report the first total synthesis of artoindonesianin B-1 (2), another member of this family, in the same route (8 steps with an overall yield of 11.3%). This discovery provides a concise route for preparing enough amounts of 1, 2, and 4 as well as 2-arylbenzo[b]furan-containing natural product-like analogs (71-74) to explore the biological potential.