65047-63-4

Basic information

• Product Name: 1-Naphthalenol, 2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-
• CAS NO: 65047-63-4
• Molecular Formula: C20H20O5
• Molecular Weight: 340.376
• Mol File: 65047-63-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenol, 2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenol, 2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-(65047-63-4)
• EPA Substance Registry System: 1-Naphthalenol, 2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-(65047-63-4)

Safety Data

• Hazardous Substances Data: 65047-63-4(Hazardous Substances Data)

Upstream product

• 58-74-2 Papaverine 
• 93-15-2 1,2-dimethoxy-4-(2-propenyl)benzene 
• 457060-10-5 2-[(E)-3-(3,4-Dimethoxy-phenyl)-propenyl]-4,5-dimethoxy-benzoic acid methyl ester 
• 64-17-5 ethanol 
• 2679-26-7 2-Methylpapaverinium iodide 
• 30034-55-0 1-(3,4-dimethoxybenzylidene)-6,7-dimethoxyisochroman-3-one 

Downstream Products

• 302587-09-3 N,N-diethyl-6-(3'-hydroxy-6',7'-dimethoxy-1',4'-dioxo-2'-naphthalenyl)-2,3-dimethoxy-benzamide 
• 302587-08-2 N,N-diethyl-6-(6',7'-dimethoxy-1',4'-dihydro-2'-naphthalenyl)-2,3-dimethoxy-benzamide 
• 302587-07-1 N,N-diethyl-6-(1'-hydroxy-6',7'-dimethoxy-2'-naphthyl)-2,3-dimethoxybenzamide 
• 40940-48-5 2-(3',4'-dimethoxyphenyl)-6,7-dimethoxy-3-hydroxy-1,4-dihydro-1,4-naphthalenedione 
• 457060-14-9 1,4-bis-(3,4-dimethoxyphenyl)-3-[2-(3,4-dimethoxyphenyl)-ethyl]-9b-hydroxy-7,8-dimethoxy-1,9b-dihydro-3H-benzo[e]indole-2,5-dione 
• 457060-08-1 2-(3,4-dimethoxyphenyl)-3-[2-(3,4-dimethoxyphenyl)-ethylamino]-6,7-dimethoxy-[1,4]-naphthoquinone 
• 322765-98-0 permethyl ningalin C 
• 302587-06-0 N,N-diethylamino-2-(3',4'-dimethoxyphenyl)-6,7-dimethoxy-1-naphthyloxymrthanone 
• 302331-54-0 2-(3',4'-dimethoxyphenyl)-6,7-dimethoxy-1,4-dihydro-1,4-naphthalenedione 

Relevant articles and documents

Efficient synthesis of ningalin C

(Matrix presented) A concise and efficient synthesis of the permethyl derivative of the marine alkaloid ningalin C (2) has been accomplished. The key step involves the formation of a pyrrolinone fron an aminoquinone in one pot. An efficient route for the

Reaction of 1-(3,4-Dimethoxybenzylidene)-6,7-dimethoxyisochroman-3-one with Lithium Aluminium Hydride: Formation of 1-(3,4-Dimethoxybenzylidene)-6,7-dimethoxyisochroman

Evidence is presented to indicate that the reductive reaction of the isochromanone derivative 1 by means of lithium aluminium hydride (LAH), yielded the isochroman 2 together with small amounts of naphthalene derivatives.All new compounds have been identi