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

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

• 118705-90-1 [1-(5,6-Diphenyl-[1,2,4]triazin-3-yl)-5-phenyl-1H-pyrazol-3-yl]-(4-nitro-phenyl)-amine 
• 118509-13-0 (Z)-2-Benzoyl-3-(2,4-dichloro-phenyl)-N-(4-nitro-phenyl)-acrylamide 
• 80392-91-2 6-Hydroxy-2-imino-1-(4-nitro-phenyl)-4-phenyl-1,2-dihydro-pyridine-3-carbonitrile 
• 80392-94-5 4,4-Dicyano-3-phenyl-but-3-enoic acid (4-nitro-phenyl)-amide 
• 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 
• 103-94-6 mono-p-nitroanilide of oxalyl acid 
• 29458-28-4 3-oxo-3-phenyl-propionic acid-(4-amino-anilide) 
• 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 

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.

Reaction of 3-Hydrazino-5,6-diphenyl-1,2,4-triazine with Unsymmetrical 1,3-Bicarbonyl Compounds : Synthesis of Some New 3-(3',5'-Disubstituted pyrazol-1'-yl)-5,6-diphenyl-1,2,4-triazines and Their Antimicrobial Activity

The reactions of 3-hydrazino-5,6-diphenyl-1,2,4-triazine (I) with unsymmetrical 1,3-bicarbonyl compounds such as α-cyanoacetophenone, benzoylacetanilide, anilino-α,β-unsaturated ketone, benzoylacetic acid hydrazide, N1-cyanoacetyl-N2-benzoylacetylhydrazine, N1-benzene-N2-benzoyl-acetylhydrazine, 1,1,1-trifluoroacetylacetone, 1,1,1,5,5,5-hexafluoropenta-2,4-dione and 1-benzoylacetone-2-oxime, have been studied in abs. ethanol, gl. acetic acid and ethanol-piperidine media.These reactions result in some new 3-(3',5'-disubstituted pyrazol-1'-yl)-5,6-diphenyl-1,2,4-triazines.Some of these compounds show moderate antimicrobial activity.