105594-89-6

Basic information

• Product Name: Formamide, N-[6-(3,4-dimethoxyphenyl)naphtho[2,3-d]-1,3-dioxol-5-yl]-N-methyl-
• CAS NO: 105594-89-6
• Molecular Formula: C21H19NO5
• Molecular Weight: 365.386
• Mol File: 105594-89-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Formamide, N-[6-(3,4-dimethoxyphenyl)naphtho[2,3-d]-1,3-dioxol-5-yl]-N-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Formamide, N-[6-(3,4-dimethoxyphenyl)naphtho[2,3-d]-1,3-dioxol-5-yl]-N-methyl-(105594-89-6)
• EPA Substance Registry System: Formamide, N-[6-(3,4-dimethoxyphenyl)naphtho[2,3-d]-1,3-dioxol-5-yl]-N-methyl-(105594-89-6)

Safety Data

• Hazardous Substances Data: 105594-89-6(Hazardous Substances Data)

Upstream product

• 105594-81-8 cis-2-(3,4-dimethoxyphenyl)-N-methyl-6,7-methylenedioxy-1,2,3,4-tetrahydro-1-naphthylamine 
• 41303-46-2 2-(3,4-dimethoxyphenyl)-6,7-methylenedioxy-3,4-dihydronaphthalen-1(2H)-one 
• 88775-45-5 (E)-1-(benzo[d][1,3]dioxol-5-yl)-3-(3,4-dimethoxyphenyl)-2-propen-1-one 
• 54022-58-1 2-(3,4-dimethoxyphenyl)-4-(3,4-methylenedioxyphenyl)-4-oxobutyronitrile 
• 6329-73-3 1-benzo[1,3]dioxol-5-yl-ethanol 
• 3162-29-6 1-(benzo[d][1,3]dioxol-6-yl)ethanone 
• 120-57-0 piperonal 
• 180411-13-6 2-(6-bromo-naphtho[2,3-d][1,3]dioxol-5-yloxy)-2-methylpropionamide 
• 213698-51-2 N-(6-bromonaphtho[2,3-d][1,3]dioxol-5-yl)-2-hydroxy-2-methylpropionamide 
• 180411-19-2 N-(6-Bromo-naphtho[2,3-d][1,3]dioxol-5-yl)-formamide 
• 180411-09-0 6,6-dibromo-7,8-dihydro-6H-naphtho[2,3-d][1,3]dioxol-5-one 
• 180411-11-4 6-bromonaphtho[2,3-d][1,3]dioxol-5-ol 
• 180411-17-0 2-bromo-6,7-methylenedioxy-1-naphthylamine 
• 41303-45-1 6,7-methylenedioxy-1-tetralone 

Downstream Products

• 52259-64-0 fagaronine 
• 88114-55-0 2-(3,4-dimethoxyphenyl)-6-hydroxy-7-methoxy-1-(N-methylformamido)naphthalene 
• 13063-04-2 nitidine chloride 

Relevant articles and documents

A versatile synthesis of fully aromatic benzo[c]phenanthridine alkaloids

A versatile new approach for the synthesis of benzo[c]phenanthridine alkaloids is described and is illustrated by the preparation of eight different alkaloids. The key steps are Smiles rearrangements, which allow easy access to 2-bromo-1-naphthylamines from 2-bromo-1-naphthols, and the attachment of the D-ring unit by Suzuki coupling.

Studies on the chemical constituents of rutaceous plants. LX. Development of a versatile method for syntheses of the antitumor benzo[c]phenanthridine alkaloids. (9). Efficient syntheses and antitumor activities of nitidine and related nonphenolic benzo[c]phenanthridine alkaloids

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