133056-55-0

Basic information

• Product Name: (-)-(R)-2-(4,5-dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxybenzaldehyde
• CAS NO: 133056-55-0
• Molecular Weight: 366.414
• Mol File: 133056-55-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (-)-(R)-2-(4,5-dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxybenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-(R)-2-(4,5-dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxybenzaldehyde(133056-55-0)
• EPA Substance Registry System: (-)-(R)-2-(4,5-dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxybenzaldehyde(133056-55-0)

Safety Data

• Hazardous Substances Data: 133056-55-0(Hazardous Substances Data)

Upstream product

• 134276-86-1 (+)-(R,4S,5S)-4,5-dihydro-2-<1<2-(1,3-dioxolan-2-yl)-4,6-dimethoxyphenyl>-4,5-dimethoxy-2-naphthyl>-4-methoxymethyl-5-phenyloxazole 
• 139077-44-4 (+)-(S)-methyl 1-<2-(1,3-dioxolan-2-yl)-4,6-dimethoxyphenyl>-4,5-dimethoxynaphthalene-2-carboxylate 
• 139077-45-5 (+)-(S)-2-<2-(2-hydroxymethyl-4,5-dimethoxy-1-naphthyl)-3,5-dimethoxyphenyl>-1,3-dioxolane 
• 133056-49-2 (+)-(4S,5S)-4-(Methoxymethyl)-5-phenyl-2-(1,4,5-trimethoxy-2-naphthyl)-4,5-dihydroxooxazole 
• 133056-53-8 1-(2-[1,3]Dioxan-2-yl-4,6-dimethoxy-phenyl)-4,5-dimethoxy-naphthalene-2-carboxylic acid methyl ester 
• 133056-54-9 (-)-(R)-2-<2-(2-Hydroxymethyl-4,5-dimethoxy-1-naphthyl)-3,5-dimethoxyphenyl>-1,3-dioxane 
• 133056-51-6 (+)-(R,4S,5S)-2-<1-<2-(1,3-Dioxan-2-yl)-4,6-dimethoxyphenyl>-4,5-dimethoxy-2-naphthyl>-4-(methoxymethyl)-5-phenyl-4,5-dihydrooxazole 
• 134984-07-9 Methanesulfonic acid 1-(2-[1,3]dioxan-2-yl-4,6-dimethoxy-phenyl)-4,5-dimethoxy-naphthalen-2-ylmethyl ester 
• 133056-53-8 1-(2-[1,3]Dioxan-2-yl-4,6-dimethoxy-phenyl)-4,5-dimethoxy-naphthalene-2-carboxylic acid methyl ester 
• 133056-54-9 (+)-S-2-<2-(2-Hydroxymethyl-4,5-dimethoxy-1-naphthyl)-3,,5-dimethoxyphenyl>-1,3-dioxane 
• 133056-51-6 (+)-(S,4S,5S)-2-<1-<2-(1,3-Dioxan-2-yl)-4,6-dimethoxyphenyl>-4,5-dimethoxy-2-naphthyl>-4-(methoxymethyl)-5-phenyl-4,5-dihydroxooxazole 
• 133056-48-1 1,4,5-Trimethoxynaphthalene-2-carboxamide 
• 133056-50-5 2-(2-Bromo-3,5-dimethoxyphenyl)-1,3-dioxane 
• 123796-58-7 1,4,5-Trimethoxynaphthalene-2-carbonitrile 

Downstream Products

• 133056-56-1 1-[2,4-Dimethoxy-6-((E)-2-nitro-propenyl)-phenyl]-4,5-dimethoxy-2-methyl-naphthalene 
• 133056-56-1 (+)-(R)-1-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-2-nitropropene 
• 133056-56-1 (-)-(S)-1-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-2-nitropropene 
• 133056-57-2 2-[2-(4,5-Dimethoxy-2-methyl-naphthalen-1-yl)-3,5-dimethoxy-phenyl]-1-methyl-ethylamine 
• 133056-57-2 (S)-2-[2-(4,5-Dimethoxy-2-methyl-naphthalen-1-yl)-3,5-dimethoxy-phenyl]-1-methyl-ethylamine 
• 133056-57-2 (R)-2-[2-(4,5-Dimethoxy-2-methyl-naphthalen-1-yl)-3,5-dimethoxy-phenyl]-1-methyl-ethylamine 
• 133056-59-4 (+)-(R,1S)-N-<2-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>-acetamide 
• 133056-59-4 (+)-(R,1R)-N-<2-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>-acetamide 
• 133056-58-3 (+)-(R,1S,3R)-N-<2-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>-4-hydroxy-3-phenylbutanamide 
• 133056-58-3 (+)-(R,1R,3R)-N-<2-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>-4-hydroxy-3-phenylbutanamide 
• 133056-57-2 2-[2-(4,5-Dimethoxy-2-methyl-naphthalen-1-yl)-3,5-dimethoxy-phenyl]-1-methyl-ethylamine 
• 133056-57-2 (S)-2-[2-(4,5-Dimethoxy-2-methyl-naphthalen-1-yl)-3,5-dimethoxy-phenyl]-1-methyl-ethylamine 
• 133056-57-2 (R)-2-[2-(4,5-Dimethoxy-2-methyl-naphthalen-1-yl)-3,5-dimethoxy-phenyl]-1-methyl-ethylamine 
• 133056-59-4 N-{2-[2-(4,5-Dimethoxy-2-methyl-naphthalen-1-yl)-3,5-dimethoxy-phenyl]-1-methyl-ethyl}-acetamide 

Relevant articles and documents

Synthetic Approaches to the Alkaloids of the Ancistrocladaceae. Part 3. The Total Synthesis of (-)-Ancistrocladinine: Control of the Diastereoisomer Excess in the Synthesis of Axially Chiral Biaryls.

The total synthesis of the naphthylisoquinoline alkaloid (-)-ancistrocladinine is described.The key step was the construction of the disymmetric bi

Synthetic Approaches to the Alkaloids of the Ancistrocladaceae: (-)-O-Methylancistrocladine and (+)-O-Methylhamatine

An asymmetric total synthesis of the naphthylisoquinoline alkaloid (-)-O-methylancistrocladine (2) is described; the synthetic method also provides routes to the atropisomer O-methylhamatine (4) and the enantiomers of these alkaloids.