62653-82-1

Basic information

• Product Name: (1R,4R,5R,8R)-4,8-bis(3,4-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane-2,6-dione
• Synonyms: (1R,4R,5R,8R)-4,8-bis(3,4-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane-2,6-dione
• CAS NO: 62653-82-1
• Molecular Weight: 414.412
• Mol File: 62653-82-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (1R,4R,5R,8R)-4,8-bis(3,4-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane-2,6-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,4R,5R,8R)-4,8-bis(3,4-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane-2,6-dione(62653-82-1)
• EPA Substance Registry System: (1R,4R,5R,8R)-4,8-bis(3,4-dimethoxyphenyl)-3,7-dioxabicyclo[3.3.0]octane-2,6-dione(62653-82-1)

Safety Data

• Hazardous Substances Data: 62653-82-1(Hazardous Substances Data)

Upstream product

• 14737-89-4 3,4-dimethoxy-trans-cinnamic acid 
• 879326-62-2 1,4-Bis-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-butane-1,4-dione 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 114125-25-6 (3S,4S)-3,4-Bis-[(3,4-dimethoxy-phenyl)-trimethylsilanyloxy-methyl]-dihydro-thiophene-2,5-dione 
• 77220-06-5 2,5-bis<(trimethylsilyl)oxy>furan 

Downstream Products

• 526-06-7 eudesmine 

Relevant articles and documents

Electochemical asymmetric dimerization of cinnamic acid derivatives and application to the enantioselective syntheses of furofuran lignans

A new electrochemical method for the asymmetric oxidative dimerization of cinnamic acid derivatives has been developed. This method enabled the enantioselective syntheses of furofuran lignans, yangambin, sesamin and eudesmin.

Reactions of Trialkylsilyl Trifluoromethanesulfonates, XII. - Aldol-Type Reactions with 2,6-Bis(trimethylsilyloxy)thiophene Synthesis of Bicyclic γ-Lactones

In the presence of trimethylsilyl triflate (2) aromatic aldehydes 4 react with 2,6-bis(trimethylsilyloxy)thiophene (3) to yield the 3,4-disubstituted thiosuccinic anhydrides 5.By hydrolysis of the products 5 in the presence of lead acetate the diaryl-subs