52392-73-1

Basic information

• Product Name: 3,4-Diphenylisoxazol-5-amine
• Synonyms: 3,4-Diphenylisoxazol-5-amine;3,4-diphenyl-1,2-oxazol-5-amine
• CAS NO: 52392-73-1
• Molecular Formula: C₁₅H₁₂N₂O
• Molecular Weight: 236.26858
• Mol File: 52392-73-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 401.3±45.0 °C(Predicted)
• Appearance: /
• Density: 1.191±0.06 g/cm3(Predicted)
• PKA: -2.08±0.50(Predicted)
• CAS DataBase Reference: 3,4-Diphenylisoxazol-5-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Diphenylisoxazol-5-amine(52392-73-1)
• EPA Substance Registry System: 3,4-Diphenylisoxazol-5-amine(52392-73-1)

Safety Data

• Hazardous Substances Data: 52392-73-1(Hazardous Substances Data)

Upstream product

• 5415-07-6 3-oxo-2,3-diphenyl-propionitrile 
• 53983-66-7 N-hydroxy-3-hydroxyamino-2,3-diphenyl-propionamidine 
• 55902-40-4 Z α-cyano β-nitrostilbene 
• 140-29-4 phenylacetonitrile 
• 934-16-7 phenylhydroxamoyl chloride 
• 873-67-6 benzonitrile oxide 
• 1071612-78-6 C₉H₈N₂ 

Downstream Products

• 52392-71-9 N-(3,4-diphenyl-isoxazol-5-yl)-acetamide 
• 52470-18-5 N-(3,4-diphenyl-isoxazol-5-yl)-diacetamide 
• 25632-70-6 5-Oxo-3,4-diphenyl-4,5-dihydroisoxazol 
• 122689-90-1 Dibenzyl-(3,4-diphenyl-isoxazol-5-yl)-amine 
• 122689-98-9 2,3-Diphenyl-2H-azirine-2-carboxylic acid dibenzylamide 
• 33859-59-5 2,3-diphenyl-2H-azirine-2-carboxamide 

Relevant articles and documents

Hoveyda-Grubbs II Catalyst: A Useful Catalyst for One-Pot Visible-Light-Promoted Ring Contraction and Olefin Metathesis Reactions

A one-pot reaction to synthesize functionalized 2H-azirines through visible-light-mediated ring contraction and olefin metathesis of isoxazoles is described. Hoveyda-Grubbs II catalyst was found to function as a photocatalyst for these transformations, al

A convenient synthesis of 4-alkyl-5-aminoisoxazoles

A series of 4-alkyl-5-aminoisoxazoles have been synthesized in high yield by nucleophilic addition of lithiated alkyl nitriles to (α)-chlorooximes. The scope and limitations of this reaction were examined by varying the nature of the nitrile and chloride