72785-28-5

Basic information

• Product Name: 4-methoxy-5-(4-methoxybenzyloxy)-benzyl acetate
• Synonyms: 4-methoxy-5-(4-methoxybenzyloxy)-benzyl acetate
• CAS NO: 72785-28-5
• Molecular Weight: 316.354
• Mol File: 72785-28-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-methoxy-5-(4-methoxybenzyloxy)-benzyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-5-(4-methoxybenzyloxy)-benzyl acetate(72785-28-5)
• EPA Substance Registry System: 4-methoxy-5-(4-methoxybenzyloxy)-benzyl acetate(72785-28-5)

Safety Data

• Hazardous Substances Data: 72785-28-5(Hazardous Substances Data)

Upstream product

• 125145-47-3 4-methoxy-5-(4-methoxybenzyloxy)benzyl alcohol 
• 75-36-5 acetyl chloride 
• 824-94-2 p-methoxybenzyl chloride 
• 72785-29-6 4-methoxy-3-((4-methoxybenzyl)oxy)benzaldehyde 
• 621-59-0 isovanillin 

Downstream Products

• 125145-48-4 2-bromo-4-methoxy-5-(4-methoxybenzyloxy)-benzylacetate 
• 1668-85-5 (-)-epigalanthamine 
• 72785-27-4 2-bromo-4-methoxy-5-(4-methoxybenzyloxy)-N-<2-(4-methoxybenzyloxyphenyl)ethyl>-N-methylbenzamide 
• 24958-44-9 2-bromo-4-methoxy-5-hydroxy-N-[2-(4-hydroxyphenyl)-ethyl]-N-methylbenzamide 
• 125145-49-5 2-bromo-4-methoxy-5-(4-methoxybenzyloxy)-benzyl alcohol 
• 72785-26-3 2-bromo-4-methoxy-5-(4-methoxybenzyloxy)-benzoic acid 
• 357-70-0 galanthamine 

Relevant articles and documents

SYNTHESIS OF GALANTHAMINE AND RELATED ALKALOIDS - NEW APPROARCHES. I.

Modifications of protecting groups and of the oxidative coupling conditions led to pure crystalline intermediates in the synthesis of galanthamine derivatives and gave dienone A in better yields than reported before.The E-configuration of amide 3' in crystalline state has been determined by X-ray diffraction.Streptomyces affinis 6737 reduces A to the optically active (-)-epigalanthamine derivative C, whose absolute configuration was determined by Bijvoet's method.Nematospora corylii CBS 2608 reduces to racemic B.With Ashbya gossypii IFO 1355 a mixture of racemic B and of optically active C is obtained.Some other microbial transformations are described.