1026854-87-4

Basic information

• Product Name: 3-{1-(4-methoxy-benzyl)-3-[2-(4-methoxy-benzyloxy)-ethyl]-1H-indol-2-yl}-1-methyl-3,4-dihydro-[2,7]naphthyridine
• Synonyms: 3-{1-(4-methoxy-benzyl)-3-[2-(4-methoxy-benzyloxy)-ethyl]-1H-indol-2-yl}-1-methyl-3,4-dihydro-[2,7]naphthyridine
• CAS NO: 1026854-87-4
• Molecular Weight: 545.681
• Mol File: 1026854-87-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-{1-(4-methoxy-benzyl)-3-[2-(4-methoxy-benzyloxy)-ethyl]-1H-indol-2-yl}-1-methyl-3,4-dihydro-[2,7]naphthyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-{1-(4-methoxy-benzyl)-3-[2-(4-methoxy-benzyloxy)-ethyl]-1H-indol-2-yl}-1-methyl-3,4-dihydro-[2,7]naphthyridine(1026854-87-4)
• EPA Substance Registry System: 3-{1-(4-methoxy-benzyl)-3-[2-(4-methoxy-benzyloxy)-ethyl]-1H-indol-2-yl}-1-methyl-3,4-dihydro-[2,7]naphthyridine(1026854-87-4)

Safety Data

• Hazardous Substances Data: 1026854-87-4(Hazardous Substances Data)

Upstream product

• 3430-22-6 3-Bromo-4-methylpyridin 
• 824-94-2 p-methoxybenzyl chloride 
• 526-55-6 2-(3-indole)-ethanol 
• 5444-01-9 3-cyano-4-methylpyridine 
• 915415-73-5 (S_s)-(E)-N-((1-(4-methoxybenzyl)-3-(2-(4-methoxybenzyloxy)ethyl)-1H-indol-2-yl)methylidene)-4-methylbenzenesulfinamide 
• 915415-72-4 1-(4-methoxybenzyl)-3-(2-(4-methoxybenzyloxy)ethyl)-1H-indole-2-carbaldehyde 
• 915415-71-3 1-(4-methoxybenzyl)-3-(2-(4-methoxybenzyloxy)ethyl)-1H-indole 
• 915415-75-7 (S_s)-(-)-N-[(1S)-2-(3-cyanopyridin-4-yl)-1-(1-(4-methoxybenzyl)-3-{2-[(4-methoxybenzyl)oxy]ethyl}-1H-indol-2-yl)-ethyl]-4-methylbenzenesulfinamide 
• 917-54-4 methyllithium 

Downstream Products

• 1025995-42-9 (1S,3S)-(-)-3-(1-(4-methoxybenzyl)-3-{2-[(4-methoxybenzyl)oxy]ethyl}-1H-indol-2-yl)-1-methyl-1,2,3,4-tetrahydro-2,7-naphthyridine 

Relevant articles and documents

Total synthesis of (-)-normalindine via addition of metalated 4-methyl-3-cyanopyridine to an enantiopure sulfinimine

A concise total asymmetric synthesis of the tetrahydronaphthyridine alkaloid (-)-normalindine has been accomplished via the addition of a laterally metalated 4-methyl-3-cyanopyridine to a sulfmimine (N-sulfmyl imine) as the key step.