62726-03-8

Basic information

• Product Name: 2-methoxy-4-nitrobenzamide
• CAS NO: 62726-03-8
• Molecular Formula: C₈H₈N₂O₄
• Molecular Weight: 196.1601
• Mol File: 62726-03-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 374.186°C at 760 mmHg
• Flash Point: 180.102°C
• Density: 1.362g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.587
• CAS DataBase Reference: 2-methoxy-4-nitrobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-4-nitrobenzamide(62726-03-8)
• EPA Substance Registry System: 2-methoxy-4-nitrobenzamide(62726-03-8)

Safety Data

• Hazardous Substances Data: 62726-03-8(Hazardous Substances Data)

Upstream product

• 39787-83-2 2-methoxy-4-nitrobenzoyl chloride 
• 2597-56-0 4-nitro-o-anisic acid 
• 619-19-2 2-hydroxy-4-nitrobenzoic acid 
• 39106-79-1 methyl 2-methoxy-4-nitrobenzoate 

Downstream Products

• 75955-30-5 4-amino-2-methoxybenzamide 
• 1319746-22-9 (Z)-2-methoxy-4-((1-(2-methoxy-4-nitrophenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)benzamide 
• 1319746-25-2 (Z)-4-((1-(2-isopropoxy-4-nitrophenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-methoxybenzamide 
• 1319746-28-5 (Z)-4-((1-(2-(benzyloxy)-4-nitrophenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-methoxybenzamide 
• 1319746-31-0 (Z)-4-((1-(4-amino-2-methoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-methoxybenzamide 
• 1319746-34-3 (Z)-4-((1-(4-amino-2-isopropoxyphenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-methoxybenzamide 
• 1319746-37-6 (Z)-4-((1-(4-amino-2-(benzyloxy)phenyl)-5-methyl-1-oxohex-2-en-3-yl)amino)-2-methoxybenzamide 
• 139632-39-6 endo-N-<<(8-methyl-8-azabicyclo<3.2.1>octan-3-yl)amino>carbonyl>-4-amino-5-chloro-2-methoxybenzamide 
• 139632-37-4 endo-N-<<(8-methyl-8-azabicyclo<3.2.1>octan-3-yl)amino>carbonyl>-4-amino-2-methoxybenzamide 
• 139632-36-3 endo-N-<<(8-methyl-8-azabicyclo<3.2.1>octan-3-yl)amino>carbonyl>-2-methoxy-4-nitrobenzamide 

Relevant articles and documents

SUBSTITUTED OXOPYRIDINE DERIVATIVES

The invention relates to substituted oxopyridine derivatives and to processes for preparation thereof, and also to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially of cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

Synthesis and antitumor activity of fused quinoline derivatives. IV. Novel 11-aminoindolo[3,2-b]quinolines

Indolo[3,2-b]quinoline derivatives (1) having various amine moieties were prepared and their antitumor activities against P388 leukemia in mice were evaluated, for the purpose of gaining an insight into the role of the amine moiety in the antitumor activity and searching for an effective amine moiety. Introduction of a methylene group between the phenyl group and amino or methanesulfonamido group resulted in decrease or loss of activity.