52028-95-2

Basic information

• Product Name: 2-Propenamide, 3-amino-3-phenyl-
• CAS NO: 52028-95-2
• Molecular Formula: C9H10N2O
• Molecular Weight: 162.191
• Mol File: 52028-95-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Propenamide, 3-amino-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenamide, 3-amino-3-phenyl-(52028-95-2)
• EPA Substance Registry System: 2-Propenamide, 3-amino-3-phenyl-(52028-95-2)

Safety Data

• Hazardous Substances Data: 52028-95-2(Hazardous Substances Data)

Upstream product

• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 100-47-0 benzonitrile 
• 3446-58-0 3-oxo-3-phenylpropanamide 
• 2216-94-6 phenylpropynoic acid ethyl ester 
• 1823-99-0 3-amino-3-phenylacrylonitrile 
• 4369-55-5 3-phenyl-isoxazol-5-ylamine 

Downstream Products

• 98179-89-6 2-(amino-phenyl-methylene)-N¹-(4-nitro-phenyl)-thiomalonamide 
• 1023694-86-1 6-(6-oxo-4-phenyl-1,6-dihydropyrimidin-2-yl)hexanoic acid 
• 92869-29-9 5-(4-nitro-anilino)-3-phenyl-isothiazole-4-carboxylic acid amide 
• 3446-58-0 3-oxo-3-phenylpropanamide 
• 84920-93-4 (Z)-3-Amino-2-(5-nitro-pyridin-2-yl)-3-phenyl-acrylamide 
• 93168-09-3 2-(Hydroxyimino)-3-oxo-3-phenylpropionamid 
• 116046-46-9 5-phenyl-4-carbamoyl-4-pyrroline-2,3-dione 
• 90563-64-7 thiobenzoyl-acetamide 
• 6632-05-9 2,5-diphenyl-1,2-dihydro-pyrazol-3-one 

Relevant articles and documents

Synthesis and Characterization of New Boron Compounds Using Reaction of Diazonium Tetraphenylborate with Enaminoamides

A family of oxazaborines, diazaborinones, triazaborines, and triazaborinones was prepared by reaction of polarized ethylenes, such as β-enaminoamides, with 4-methylbenzenediazo-nium tetraphenylborates. The reaction conditions (stirring in CH2Cl2 at room temperature (Method A) or stirring with CH3COONa in CH2Cl2 at room temperature (Method B) or refluxing in the CH2Cl2/toluene mixture (Method C)) controlled the formation and relative content of these compounds in the reaction mixtures from one to three products. Substituted oxazaborines gradually rearranged into diazaborinones at 250 °C. The prepared compounds were characterized by1H NMR,13C NMR, IR, and UV–Vis spectroscopy, HRMS, or microanalysis. The structure of individual compounds was confirmed by11B NMR,15N NMR, 1D NOESY, and X-ray analysis. The mechanism of reaction of enaminoamides with 4-methylbenzenediazonium tetraphenylborate was proposed.

β Aminocinnamonitriles as potential antiinflammatory agents

A number of β aminocinnamonitriles have been prepared by the reaction of salts of acetonitrile and proprionitrile with benzonitrile. These materials were evaluated in the carrageenan antiinflammatory screen in Royal Hart, Wistar strain rats. Despite food weight gains with the parent molecule, β aminocinnamonitrile, only marginal activity was found in related compounds and some possible 'metabolites'.