15440-38-7

Basic information

• Product Name: N-[3-oxo-1-phenyl-3-(phenylamino)prop-1-en-2-yl]benzamide
• CAS NO: 15440-38-7
• Molecular Formula: C₂₂H₁₈N₂O₂
• Molecular Weight: 342.3905
• Mol File: 15440-38-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 635.3°C at 760 mmHg
• Flash Point: 227.2°C
• Density: 1.24g/cm³
• Vapor Pressure: 4.84E-16mmHg at 25°C
• Refractive Index: 1.681
• CAS DataBase Reference: N-[3-oxo-1-phenyl-3-(phenylamino)prop-1-en-2-yl]benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[3-oxo-1-phenyl-3-(phenylamino)prop-1-en-2-yl]benzamide(15440-38-7)
• EPA Substance Registry System: N-[3-oxo-1-phenyl-3-(phenylamino)prop-1-en-2-yl]benzamide(15440-38-7)

Safety Data

• Hazardous Substances Data: 15440-38-7(Hazardous Substances Data)

Upstream product

• 842-74-0 4-benzylidene-2-phenyloxazole-5(4H)-one 
• 62-53-3 aniline 
• 17606-70-1 (4Z)-4-benzylidene-2-phenyl-1,3-oxazol-5(4H)-one 
• 495-69-2 Hippuric Acid 
• 100-52-7 benzaldehyde 
• 18510-74-2 4-benzylidene-2,6-diphenyl-4H-[1,2,5]oxadiazin-3-one 
• 1199-01-5 2-phenylazlactone 
• 538-51-2 benzylidene phenylamine 
• 16446-30-3 4-benzylidene-2-phenyl-4H-thiazol-5-one 
• 18510-92-4 N-hydroxy-3,N-diphenyl-2-thiobenzoylamino-acrylamide 

Downstream Products

• 36917-07-4 (4-benzylidene-2-phenyl-4H-oxazol-5-ylidene)-phenyl-amine 

Relevant articles and documents

Solid supported reaction of substituted 2-oxazoline with amines under microwave irradiation

1,2-Diaryl-4-phenylmethylene-2-imidazolin-5-ones were obtained by the interaction of primary amines with 2-phenyl-4-phenylmethylene-2-oxazolin-5-one using acidic alumina or montmorillonite K10 clay under microwave irradiation (MWI). The same reaction over

A fast and facile synthesis of n-substituted 2-acylaminoprop-2- enamides using unsaturated azlactones as synthons

A modified route for the fast and facile synthesis of N-substituted 2-acylaminopro- 2-enamides (4) is hereby developed. The conversion of α -N-acylglycine (1) to unstable 2-substituted 2-oxazolin-5-ones (2) was carried out at room temp using ptoluenesulph