1196996-66-3

Basic information

• Product Name: (3-(benzyloxy)-6-(((S)-7-(benzyloxy)-1,2,3,4-tetrahydro-6-methoxyisoquinolin-1-yl)-methyl)-2-methoxyphenyl)methanol
• Synonyms: (3-(benzyloxy)-6-(((S)-7-(benzyloxy)-1,2,3,4-tetrahydro-6-methoxyisoquinolin-1-yl)-methyl)-2-methoxyphenyl)methanol
• CAS NO: 1196996-66-3
• Molecular Weight: 525.645
• Mol File: 1196996-66-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (3-(benzyloxy)-6-(((S)-7-(benzyloxy)-1,2,3,4-tetrahydro-6-methoxyisoquinolin-1-yl)-methyl)-2-methoxyphenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3-(benzyloxy)-6-(((S)-7-(benzyloxy)-1,2,3,4-tetrahydro-6-methoxyisoquinolin-1-yl)-methyl)-2-methoxyphenyl)methanol(1196996-66-3)
• EPA Substance Registry System: (3-(benzyloxy)-6-(((S)-7-(benzyloxy)-1,2,3,4-tetrahydro-6-methoxyisoquinolin-1-yl)-methyl)-2-methoxyphenyl)methanol(1196996-66-3)

Safety Data

• Hazardous Substances Data: 1196996-66-3(Hazardous Substances Data)

Upstream product

• 63909-38-6 3-methoxy-4-benzyloxy-ω-nitrostyrolene 
• 1196996-64-1 3-(benzyloxy)-6-((7-(benzyloxy)-3,4-dihydro-6-methoxyisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate 
• 1196996-63-0 6-((4-(benzyloxy-3-methoxyphenethyl)carbamoyl)methyl)-3-(benzyloxy)-2-methoxybenzyl acetate 
• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 65615-24-9 N-(4-(benzyloxy)-3-methoxyphenethyl)-2-(4-(benzyloxy)-2-(hydroxymethyl)-3-methoxyphenyl)acetamide 
• 65615-22-7 7-(benzyloxy)-8-hydroxy-1H-isochromen-3(4H)-one 
• 28988-68-3 2-(4-(benzyloxy)-3-hydroxyphenyl)acetic acid 
• 100-39-0 benzyl bromide 
• 101111-25-5 methyl 2-(4-(benzyloxy)-3-bromophenyl)acetate 
• 121-33-5 vanillin 
• 34918-57-5 methyl 3-bromo-4-hydroxyphenylacetate 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 22231-61-4 2-[4-(benzyloxy)-3-methoxyphenyl]ethylamine 
• 1196996-65-2 3-(benzyloxy)-6-(((S)-7-(benzyloxy)-1,2,3,4-tetrahydro-6-methoxyisoquinolin-1-yl)methyl)-2-methoxybenzyl acetate 

Downstream Products

• 1258935-42-0 C₃₃H₃₄ClNO₄ 
• 16562-14-4 (-)-stepholidine 
• 1196996-62-9 (S)-2,10-dibenzyloxy-3,9-dimethoxytetrahydroprotoberberine 

Relevant articles and documents

Asymmetric total synthesis of tetrahydroprotoberberine derivatives and evaluation of their binding affinities at dopamine receptors

Cocaine addiction remains a serious challenge for clinical and medical research because there is no effective pharmacological treatment. L-THP, a natural product isolated from Corydalis yanhusuo W.T. Wang, is one of the most frequently used traditional herbs to treat drug addiction in China. Our laboratory first reported that its demethylated metabolites L-ICP, L-CD, and L-CP had high affinity at dopamine D1, D2, and D5 receptors. Here we report the chemical synthesis of these metabolites and other derivatives and their binding affinities at dopamine receptors. The synthesis of these bioactive metabolites will allow further in vivo study of their potential in treating cocaine addiction.

Enantioselective total synthesis of (-)-(S)-stepholidine

(Chemical Equation Presented) Enantioselective total synthesis of (-)-(S)-stepholidine, a drug candidate for the treatment of schizophrenia and/or drug abuse, is described. Asymmetric transfer hydrogenation of imines with use of Noyori's catalyst was used