88114-54-9

Basic information

• Product Name: Formamide, N-[2-(3,4-dimethoxyphenyl)-7-methoxy-6-(1-methylethoxy)-1-naphthalen yl]-N-methyl-
• CAS NO: 88114-54-9
• Molecular Formula: C24H27NO5
• Molecular Weight: 409.482
• Mol File: 88114-54-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Formamide, N-[2-(3,4-dimethoxyphenyl)-7-methoxy-6-(1-methylethoxy)-1-naphthalen yl]-N-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Formamide, N-[2-(3,4-dimethoxyphenyl)-7-methoxy-6-(1-methylethoxy)-1-naphthalen yl]-N-methyl-(88114-54-9)
• EPA Substance Registry System: Formamide, N-[2-(3,4-dimethoxyphenyl)-7-methoxy-6-(1-methylethoxy)-1-naphthalen yl]-N-methyl-(88114-54-9)

Safety Data

• Hazardous Substances Data: 88114-54-9(Hazardous Substances Data)

Upstream product

• 88114-53-8 cis-2-(3,4-dimethylphenyl)-6-isopropoxy-7-methoxy-N-methyl-1,2,3,4-tetrahydronaphthalen-1-amine 
• 113964-89-9 2-(3,4-dimethoxyphenyl)-4-(3'-isopropyloxy-4'-methoxy)phenyl butyric acid 
• 113964-91-3 2-(3,4-dimethoxyphenyl)-6-isopropyloxy-7-methoxy-3,4-dihydronaphthalen-1(2H)-one 
• 88114-46-9 2-(3,4-dimethoxyphenyl)-4-(3-isopropoxy-4-methoxyphenyl)-4-oxobutyronitrile 
• 88114-47-0 2-(3,4-dimethoxyphenyl)-4-(3-isopropoxy-4-methoxyphenyl)-4-oxobutyric acid 
• 88114-52-7 [2-(3,4-Dimethoxy-phenyl)-6-isopropoxy-7-methoxy-3,4-dihydro-2H-naphthalen-(1Z)-ylidene]-methyl-amine 
• 88114-45-8 3'-isopropoxy-3,4,4'-trimethoxychalcone 
• 113964-90-2 1-(3-isopropoxy-4-methoxyphenyl)ethanol 
• 621-59-0 isovanillin 
• 88114-56-1 cis-2-(3,4-dimethoxyphenyl)-6-isopropoxy-7-methoxy-1-(N-methyl-formamido)-1,2,3,4-tetrahydronaphthalene 

Downstream Products

• 52259-64-0 fagaronine 
• 88114-55-0 2-(3,4-dimethoxyphenyl)-6-hydroxy-7-methoxy-1-(N-methylformamido)naphthalene 

Relevant articles and documents

Studies on the Chemical Constituents of Rutaceous Plants. Part 62. Efficient Synthesis of Fagaronine, a Phenolic Benzophenanthridine Alkaloid with Antileukaemic Activity

Fagarinone (2), an antileukaemic hydroxybenzophenanthridine alkaloid, has been synthesized from the chalcone (4a) according to the synthetic sequence (Schemes 1-4).During the synthesis, the hydroxy group was protected in the form of its isopropoxy deri