1260158-09-5

Basic information

• Product Name: 1-(4-isopropoxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline
• Synonyms: 1-(4-isopropoxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline
• CAS NO: 1260158-09-5
• Molecular Weight: 355.477
• Mol File: 1260158-09-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-isopropoxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-isopropoxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline(1260158-09-5)
• EPA Substance Registry System: 1-(4-isopropoxybenzyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline(1260158-09-5)

Safety Data

• Hazardous Substances Data: 1260158-09-5(Hazardous Substances Data)

Upstream product

• 1070165-27-3 4-isopropoxyphenylacetaldehyde 
• 35690-71-2 [2-(3,4-dimethoxy-phenyl)-ethyl]-carbamic acid methyl ester 
• 50-00-0 formaldehyd 
• 1260158-11-9 1-(4-isopropoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 

Downstream Products

• 5884-67-3 armepavine 

Relevant articles and documents

Total synthesis of (±)-armepavines and (±)-nuciferines from (2-nitroethenyl)benzene derivatives

A concise route to armepavine 1 and nuciferine 2 and 3, which can be isolated from the leaves of Nelumbo nucifera (Nymphaceae), has been achieved in which the longest linear sequence is only six steps from commercially available benzaldehyde in 28%, 21%, and 20% overall yield, respectively. The key transformations in the synthesis are the radical cyclization of aryl bromide with Bu3SnH and the Pictet-Spengler reaction of N-substituted amine with aldehyde. Copyright Taylor & Francis Group, LLC.