88205-41-8

Basic information

• Product Name: Isoquinolinium,2-(acetylamino)-1-[(3,4-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-, iodide
• CAS NO: 88205-41-8
• Molecular Formula: C23H31N2O5.I
• Molecular Weight: 542.414
• Mol File: 88205-41-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Isoquinolinium,2-(acetylamino)-1-[(3,4-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-, iodide(CAS DataBase Reference)
• NIST Chemistry Reference: Isoquinolinium,2-(acetylamino)-1-[(3,4-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-, iodide(88205-41-8)
• EPA Substance Registry System: Isoquinolinium,2-(acetylamino)-1-[(3,4-dimethoxyphenyl)methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-, iodide(88205-41-8)

Safety Data

• Hazardous Substances Data: 88205-41-8(Hazardous Substances Data)

Upstream product

• 88205-40-7 N-acetamidopapaverinium iodide 
• 88205-39-4 1-(3',4'-dimethoxybenzyl)-6,7-dimethoxy-2-(N-methylacetamido)isoquinolinium iodide 
• 88205-38-3 N-aminopapaverinium mesitylenesulphate 
• 88205-34-9 2-acetamido-1-(3',4'-dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 88205-35-0 1-(3',4'-dimethoxybenzyl)-6,7-dimethoxy-2-(N-methylacetamido)-1,2-dihydroisoquinoline 
• 88205-33-8 2-amino-1-(3',4'-dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 58-74-2 Papaverine 
• 88205-36-1 1-(3',4'-dimethoxybenzyl)-6,7-dimethoxy-2-(N-methylacetamido)-1,2,3,4-tetrahydroisoquinoline 
• 74-88-4 methyl iodide 

Downstream Products

• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 16620-96-5 2-methyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Electrochemical Oxidation of Aromatic Ethers. Part 8. Evidence of Homogeneous Electron Transfer during the 'Low Potential' Oxidation of Laudanosine

Photolysis of N-amino- and N-nitroso-derivatives of 1,2,3,4-tetrahydropapaverine fails to produce aryl-aryl coupled products analogous to O-methylflavinantine.Instead both the 1- and 2-substituents of the heterocyclic ring are cleaved to give 6,7-dimethoxy-3,4-dihydroisoquinolines and veratraldehyde, the latter being an oxidation product of the 3,4-dimethoxybenzyl radical and/or cation.From this evidence, and the results of an electrolysis experiment carried out at high dilution, it is considered that the anodic cyclisation of laudanosine to O-methylflavinantine proceeds through homogeneous electron transfer rather than via homoconjugative activation within the intermediate radical cation as proposed by other workers.