103047-73-0

Basic information

• Product Name: α-<3.4.5-Trimethoxy-benzyliden>-β-<3.4.5-trimethoxy-benzyl>-γ-butyrolacton
• Synonyms: α-<3.4.5-Trimethoxy-benzyliden>-β-<3.4.5-trimethoxy-benzyl>-γ-butyrolacton
• CAS NO: 103047-73-0
• Molecular Weight: 444.482
• Mol File: 103047-73-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: α-<3.4.5-Trimethoxy-benzyliden>-β-<3.4.5-trimethoxy-benzyl>-γ-butyrolacton(CAS DataBase Reference)
• NIST Chemistry Reference: α-<3.4.5-Trimethoxy-benzyliden>-β-<3.4.5-trimethoxy-benzyl>-γ-butyrolacton(103047-73-0)
• EPA Substance Registry System: α-<3.4.5-Trimethoxy-benzyliden>-β-<3.4.5-trimethoxy-benzyl>-γ-butyrolacton(103047-73-0)

Safety Data

• Hazardous Substances Data: 103047-73-0(Hazardous Substances Data)

Upstream product

• 65171-10-0 (+/-)-4-(3,4,5-trimethoxyphenyl)-4,5-dihydro-2(3H)-furanone 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 76763-88-7 (R)-dihydro-4-(3,4,5-trimethoxybenzyl)furan-2(3H)-one 

Downstream Products

• 7432-28-2 6(SR),7(RS)-5,6,7,8-tetrahydro-7-hydroxy-1,2,3,10,11,12-hexamethoxy-6,7-dimethyldibenzocyclooctene 
• 7432-28-2 isoschizandrin 

Relevant articles and documents

Synthesis of optically pure gomisin A and schizandrin: The first total synthesis of gomisin A and schizandrin having naturally occurring configurations

The total synthesis of gomisin A and schizandrin having natural configurations were accomplished for the first time. The key feature of these syntheses is a highly efficient intramolecular oxidative coupling of the intermediates 9 and 21, which can be obtained as both enantiomers in optically pure forms. The manipulation of the lactone moieties of 7 and 22 afforded natural enantiomers of schizandrin and gomisin A.