126893-26-3

Basic information

• Product Name: 2-Nitro-3,5-dimethoxy-ω-diazoacetophenone
• CAS NO: 126893-26-3
• Molecular Weight: 251.199
• Mol File: 126893-26-3.mol

Chemical Properties

• CAS DataBase Reference: 2-Nitro-3,5-dimethoxy-ω-diazoacetophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Nitro-3,5-dimethoxy-ω-diazoacetophenone(126893-26-3)
• EPA Substance Registry System: 2-Nitro-3,5-dimethoxy-ω-diazoacetophenone(126893-26-3)

Safety Data

• Hazardous Substances Data: 126893-26-3(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 109069-76-3 3,5-dimethoxy-2-nitrobenzoyl chloride 
• 113884-71-2 Acide 2-nitro-3,5-dimethoxybenzoique 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 
• 76746-30-0 2-Nitro-3,5-dimethoxybenzoate de methyle 
• 1132-21-4 3,5-dimethoxybenzoic acid 

Downstream Products

• 126893-21-8 N-(2-Benzo[1,3]dioxol-5-yl-ethyl)-2-(3,5-dimethoxy-2-nitro-phenyl)-acetamide 
• 102652-89-1 3,5-dimethoxy-2-nitroacetophenone 
• 23042-76-4 2-amino-3,5-dimethoxyacetophenone 
• 126893-22-9 1-(2-nitro-3,5-dimethoxy-benzyl)-6,7-methylenedioxy-3,4-dihydroisoquinoline 
• 131653-15-1 2,4-Dimethoxy-6-(6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-ylmethyl)-phenylamine 
• 131653-14-0 5-[1-(3,5-Dimethoxy-2-nitro-phenyl)-meth-(Z)-ylidene]-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline 
• 131653-16-2 5-(3,5-Dimethoxy-2-nitro-benzyl)-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline 
• 131653-13-9 5-(3,5-Dimethoxy-2-nitro-benzyl)-6-methyl-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinolin-6-ium; iodide 

Relevant articles and documents

Alkaloids from Annonaceae 93. First synthesis of a meta-disubstituted aporphine

The synthesis of a new aporphinoid alkaloid, substituted on the 9 and 11 positions, is reported.An unexpected reactivity has been observed for several intermediates.It has been attributed to the position of the methoxy groups with regard to the nitro group.

Obtention of Anthranil Derivatives by a Modified Bischler-Napieralsky Reaction.

The action of PCl5 or POCl3 on substituted 2-nitro-3,5-dimethoxyphenylacetamide gives 5,7-dimethoxy-2,1-benzisoxazole derivatives in high yields, even in the absence of any alkaline treatment.This special reactivity is due to the position of the two metho