128429-03-8

Basic information

• Product Name: Methyl 3-nitro-4-(propylaMino)benzoate
• Synonyms: Methyl 3-nitro-4-(propylaMino)benzoate
• CAS NO: 128429-03-8
• Molecular Formula: C₁₁H₁₄N₂O₄
• Molecular Weight: 238.23986
• Mol File: 128429-03-8.mol
• Article Data: 7

Chemical Properties

• Melting Point: 62-64 °C
• Boiling Point: 384.1±32.0 °C(Predicted)
• Appearance: /
• Density: 1.243±0.06 g/cm3(Predicted)
• PKA: -2.66±0.50(Predicted)
• CAS DataBase Reference: Methyl 3-nitro-4-(propylaMino)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 3-nitro-4-(propylaMino)benzoate(128429-03-8)
• EPA Substance Registry System: Methyl 3-nitro-4-(propylaMino)benzoate(128429-03-8)

Safety Data

• Hazardous Substances Data: 128429-03-8(Hazardous Substances Data)

Upstream product

• 96-99-1 4-chloro-3-nitrobenzoate 
• 107-10-8 propylamine 
• 329-59-9 4-fluoro-3-nitro-benzoic acid methyl ester 
• 14719-83-6 methyl 3-nitro-4-chlorobenzoate 
• 453-71-4 3-nitro-4-fluorobenzoic acid 
• 67-56-1 methanol 
• 68740-31-8 3-nitro-N⁴-propylaminobenzoic acid 

Downstream Products

• 762295-22-7 methyl 3-amino-4-(propylamino)benzoate 

Relevant articles and documents

Modulating catalytic activity of a modified flavin analogue: Via judicially positioned metal ion toward aerobic sulphoxidation

This manuscript describes the synthesis, spectroscopic and crystallographic characterization of a cadmium complex of 10-propoylisoalloxazine-7-carboxylic acid (Flc-Cd). Catalytic activity of Flc-Cd towards aerobic sulphoxidation reaction was investigated in the presence of l-ascorbic acid as the reducing agent. Notably the neutral un-metalated flavin analogue did not show any significant catalytic activity. The design strategy for Flc provides a close proximity of the metal centre to the flavin core without compromising the catalytic site thereby assisting the product formation when compared to unmetallated Flc. Minor enantioselectivity is also observed in cases where unsymmetrical sulphides were used; indicative of the possible involvement of chiral l-ascorbic acid in the intermediate formation. This journal is

Copper catalyzed aerobic oxidative cyclization and ketonization: One pot synthesis of benzoimidazo[1,2-: A] imidazolones

A highly efficient synthesis of benzoimidazo[1,2-a]imidazolone through a novel oxidative 5-exo-dig cyclization-ketonization cascade of 2-aminobenzimidazole, aldehyde and terminal alkyne has been explored under aerobic conditions. The reaction proceeds thr

A concise synthesis of 2-(2-aminothiophene)-benzimidazoles by one-pot multicomponent reaction

A one-pot synthesis of 2-aminothiophene linked benzimidazoles was achieved by utilizing 2-cyanomethyl benzimidazoles in a modified Gewald multicomponent reaction. The synthetic strategy of the reaction involved treatment of 2-(cyanomethyl)-benzimdazole wi