968-29-6

Basic information

• Product Name: N-(4-nitrophenyl)-3-oxo-3-phenylpropanamide
• CAS NO: 968-29-6
• Molecular Formula: C₁₅H₁₂N₂O₄
• Molecular Weight: 284.2668
• Mol File: 968-29-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 554°C at 760 mmHg
• Flash Point: 288.9°C
• Density: 1.351g/cm³
• Vapor Pressure: 2.57E-12mmHg at 25°C
• Refractive Index: 1.649
• CAS DataBase Reference: N-(4-nitrophenyl)-3-oxo-3-phenylpropanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-nitrophenyl)-3-oxo-3-phenylpropanamide(968-29-6)
• EPA Substance Registry System: N-(4-nitrophenyl)-3-oxo-3-phenylpropanamide(968-29-6)

Safety Data

• Hazardous Substances Data: 968-29-6(Hazardous Substances Data)

Upstream product

• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 110194-21-3 1-benzenesulfonylamino-4-(3-oxo-3-phenyl-propionylamino)-benzene 
• 113381-03-6 1-benzoylamino-4-(3-oxo-3-phenyl-propionylamino)-benzene 
• 118533-90-7 5-(2,4-Dichloro-phenyl)-1-(5,6-diphenyl-[1,2,4]triazin-3-yl)-3-phenyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid (4-nitro-phenyl)-amide 
• 118509-17-4 (Z)-3-(2,4-Dichloro-phenyl)-2-{[(5,6-diphenyl-[1,2,4]triazin-3-yl)-hydrazono]-phenyl-methyl}-N-(4-nitro-phenyl)-acrylamide 
• 103-94-6 mono-p-nitroanilide of oxalyl acid 
• 80392-87-6 2-Hydroxy-6-(4-nitro-phenylamino)-4-phenyl-nicotinonitrile 
• 80392-83-2 2-{Amino-[6-(4-nitro-phenylamino)-2-oxo-4-phenyl-2H-pyridin-(3Z)-ylidene]-methyl}-malononitrile 
• 80392-94-5 4,4-Dicyano-3-phenyl-but-3-enoic acid (4-nitro-phenyl)-amide 
• 80392-91-2 6-Hydroxy-2-imino-1-(4-nitro-phenyl)-4-phenyl-1,2-dihydro-pyridine-3-carbonitrile 
• 118509-13-0 (Z)-2-Benzoyl-3-(2,4-dichloro-phenyl)-N-(4-nitro-phenyl)-acrylamide 
• 118705-90-1 [1-(5,6-Diphenyl-[1,2,4]triazin-3-yl)-5-phenyl-1H-pyrazol-3-yl]-(4-nitro-phenyl)-amine 
• 29458-28-4 3-oxo-3-phenyl-propionic acid-(4-amino-anilide) 

Relevant articles and documents

Selective exploitation of acetoacetate carbonyl groups using imidazolium based ionic liquids: synthesis of 3-oxo-amides and substituted benzimidazoles

An unprecedented Br?nsted base ionic liquid tuned selective aminolysis of ester carbonyl of acetoacetates is demonstrated to achieve acetoacetamide derivatives. Other imidazolium ionic liquid performs an efficient cyclization catalysis involving acetoacetate-carbonyl groups and o-phenylenediamine at elevated temperature to produce benzimidazoles via C–C bond cleavage of intermediate 1,5-benzodiazepinones under solvent-free conditions.