79831-92-8

Basic information

• Product Name: 5-benzyloxy-4-methoxy-2-nitro-N-(3,4,5-trimethoxyphenethyl)phenylacetamide
• CAS NO: 79831-92-8
• Molecular Weight: 510.544
• Mol File: 79831-92-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-benzyloxy-4-methoxy-2-nitro-N-(3,4,5-trimethoxyphenethyl)phenylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 5-benzyloxy-4-methoxy-2-nitro-N-(3,4,5-trimethoxyphenethyl)phenylacetamide(79831-92-8)
• EPA Substance Registry System: 5-benzyloxy-4-methoxy-2-nitro-N-(3,4,5-trimethoxyphenethyl)phenylacetamide(79831-92-8)

Safety Data

• Hazardous Substances Data: 79831-92-8(Hazardous Substances Data)

Upstream product

• 78792-73-1 5-benzyloxy-4-methoxy-2-nitrophenylacetic acid 
• 54-04-6 mescaline 
• 99613-07-7 5-benzyloxy-4-methoxy-2-nitrophenylacetyl chloride 
• 5487-33-2 O-benzylhomoisovanillic acid 

Downstream Products

• 79832-21-6 1-(2-amino-5-benzyloxy-4-methoxybenzyl)-1,2,3,4-tetrahydro-6,7,8-trimethoxy-2-methylisoquinoline 
• 549-28-0 protostephanine 
• 20824-18-4 protostephanone 
• 79832-12-5 1-(5-benzyloxy-4-methoxy-2-nitrobenzyl)-3,4-dihydro-6,7,8-trimethoxyisoquinoline 

Relevant articles and documents

Synthesis along Biosynthetic Pathways. Part 2. Synthesis of Protostephanine

The dienone protostephanone (3) is synthesised by phenol coupling or by Pschorr cyclisation from readily prepared tetrahydroisoquinolines, and the corresponding dienols (17) and (18) are converted by rearrangement, fragmentation, and reduction into protostephanine (4).This sequence mimics the natural pathway to the alkaloid.