292820-07-6

Basic information

• Product Name: (2S,5R)-2-tert-Butyldiphenylsilyloxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)non-5'-enyl)tetrahydrofuran
• Synonyms: (2S,5R)-2-tert-Butyldiphenylsilyloxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)non-5'-enyl)tetrahydrofuran
• CAS NO: 292820-07-6
• Molecular Weight: 674.993
• Mol File: 292820-07-6.mol

Chemical Properties

• CAS DataBase Reference: (2S,5R)-2-tert-Butyldiphenylsilyloxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)non-5'-enyl)tetrahydrofuran(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,5R)-2-tert-Butyldiphenylsilyloxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)non-5'-enyl)tetrahydrofuran(292820-07-6)
• EPA Substance Registry System: (2S,5R)-2-tert-Butyldiphenylsilyloxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)non-5'-enyl)tetrahydrofuran(292820-07-6)

Safety Data

• Hazardous Substances Data: 292820-07-6(Hazardous Substances Data)

Upstream product

• 292820-05-4 4-(2',3',4',5'-Tetramethoxy-6'-methylphenyl)-4-oxobutyric acid 
• 292820-15-6 1-(1',4'-Dihydroxybutyl)-2,3,4,5-tetramethoxy-6-methylbenzene 
• 80810-55-5 1-(4'-Hydroxybutyl)-2,3,4,5-tetramethoxy-6-methylbenzene 
• 35896-58-3 2,3,4,5-tetramethoxytoluene 
• 80810-40-8 1-(4'-Oxobutyl)-2,3,4,5-tetramethoxy-6-methylbenzene 

Downstream Products

• 337954-04-8 19-O,23-O-Di-(tert-butyldimethylsilyl)hydroquinone-mucocin dimethyl ether 
• 292820-09-8 Hydroquinone-mucocin dimethyl ether 
• 292820-17-8 (2S,5R)-2-Hydroxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)nonyl)tetrahydrofuran 
• 292820-08-7 (2S,5R)-2-Formyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)nonyl)tetrahydrofuran 
• 292820-16-7 (2S,5R)-2-tert-Butyldiphenylsilyloxymethyl-5-(9'-(2'',3'',4'',5''-tetramethoxy-6''-methylphenyl)nonyl)tetrahydrofuran 

Relevant articles and documents

Natural-product hybrids: Design, synthesis, and biological evaluation of quinone - Annonaceous acetogenins

Replacement of the butyrolactone unit of the natural products with a quinone subunit has resulted in the synthesis of natural-product hybrids of quinone-mucocin (1). These compounds, which are combined from partial structures of annonaceous acetogenins an