123878-26-2

Basic information

• Product Name: ancistrocladisine
• CAS NO: 123878-26-2
• Molecular Weight: 419.521
• Mol File: 123878-26-2.mol

Chemical Properties

• CAS DataBase Reference: ancistrocladisine(CAS DataBase Reference)
• NIST Chemistry Reference: ancistrocladisine(123878-26-2)
• EPA Substance Registry System: ancistrocladisine(123878-26-2)

Safety Data

• Hazardous Substances Data: 123878-26-2(Hazardous Substances Data)

Upstream product

• 123796-68-9 N-<2-<4-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>acetamide 
• 31558-40-4 4-bromo-3,5-dimethoxybenzaldehyde 
• 123796-59-8 1,4,5-Trimethoxynaphthalene-2-carboxylic Acid 
• 123796-62-3 2-<1-<4-(1,3-Dioxolan-2-yl)-2,6-dimethoxyphenyl>-4,5-dimethoxy-2-naphthyl>-4,4-dimethyl-4,5-dihydrooxazole 
• 134822-51-8 Methyl 1-<2,6-Dimethoxy-4-((E)-2-nitropropenyl)phenyl>-4,5-dimethoxynaphthalene-2-carboxylate 
• 123796-60-1 4,5-Dihydro-4,4-dimethyl-2(1,4,5-trimethoxy-2-naphthyl)-oxazole 
• 186581-53-3 diazomethane 
• 123796-61-2 2-(4-bromo-3,5-dimethoxyphenyl)-[1,3]dioxolane 
• 107941-22-0 2-bromo-1,4,5-trimethoxynaphthalene 
• 123796-58-7 1,4,5-Trimethoxynaphthalene-2-carbonitrile 
• 77189-69-6 5-acetoxy-2-bromo-1,4-naphthoquinone 
• 123796-64-5 1-[2,6-Dimethoxy-4-((Z)-2-nitro-propenyl)-phenyl]-4,5-dimethoxy-naphthalene-2-carboxylic acid methyl ester 
• 123796-66-7 Acetic acid 1-[4-(2-acetylamino-propyl)-2,6-dimethoxy-phenyl]-4,5-dimethoxy-naphthalen-2-ylmethyl ester 
• 123796-67-8 N-<2-<2-(Hydroxymethyl-4,5-dimethoxy-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>acetamide 

Relevant articles and documents

Ancistrobertsonines B, C, and D as well as 1,2- didehydroancistrobertsonine D from Ancistrocladus robertsoniorum

From the East African Liana Ancistrocladus robertsoniorum, four new naphthylisoquinoline alkaloids have been isolated using High Speed Countercurrent Chromatography (HSCCC) and High Performance Liquid Chromatography (HPLC). Their stereostructures were established by spectroscopic, chemical, and chiroptical methods. Two of the new compounds, ancistrobertsonines B and C, constitute O- and N-permethylated 5,1'-coupled and 5,8'-coupled regioisomeric naphthylisoquinolines, while ancistrobertsonine D and its 1,2-didehydro analogue are based on a 7,1'- coupling mode between the isoquinoline and naphthalene moieties. Biological tests revealed that some of the isolated alkaloids possess moderate antimalarial activities.

Synthetic Approaches to the Naphthyl-isoquinoline Alkaloids. Part 1. Dehydroancistrocladisine

A synthesis of (+/-)-7-(4,5-dimethoxy-2-methyl-1-naphthyl)-6,8-dimethoxy-1,3-dimethylisoqinoline (dehydroancistrocladisine) 19, the racemic form of a degradation product of the unusual naphthylisoquinoline alkaloid ancistrocladisine 3, is recorded.The key

Synthetic Approaches to the Alkaloids of the Ancistrocladacea: Dehydroancistrocladisine

Dehydroancistrocladisine, a derivative of ancistrocladisine which is a member of the unusual naphthyl-isoquinoline group of alkaloids, has been synthesized by a route which can be adapted to provide asymmetric syntheses of thes alkaloids.