5679-59-4

Basic information

• Product Name: Phosphenimidous amide,N,N'-diphenyl-
• Synonyms: Phosphine,anilino(phenylimino)- (5CI); NSC 5726
• CAS NO: 5679-59-4
• Molecular Formula: C12H11 N2 P
• Molecular Weight: 214.207
• Mol File: 5679-59-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• CAS DataBase Reference: Phosphenimidous amide,N,N'-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphenimidous amide,N,N'-diphenyl-(5679-59-4)
• EPA Substance Registry System: Phosphenimidous amide,N,N'-diphenyl-(5679-59-4)

Safety Data

• Hazardous Substances Data: 5679-59-4(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 

Downstream Products

• 17645-30-6 (E)-crotonanilide 
• 4424-17-3 2-aminobenzanilide 
• 885657-93-2 4-(2-methyl-4-oxo-4H-quinazolin-3-yl)-N-phenyl-butyramide 
• 14664-84-7 3-methyl-4-phenyl-5-(2-pyridyl)-1,2,4-triazole 
• 948854-58-8 3-isopropyl-4-phenyl-5-(2-(phenylselanyl)ethyl)-4H-[1,2,4]triazole 
• 948854-51-1 3-benzyl-4-phenyl-5-(2-(phenylselanyl)ethyl)-4H-[1,2,4]triazole 
• 2210-24-4 N-acryloylaniline 
• 54639-27-9 N-phenyl-2-hydroxy-3-methyl-butanamide 

Relevant articles and documents

Synthesis and properties of 1,2-dihydro-4(3H)-quinazolinones

We modified the preparative-scale method for the synthesis of 2-aryl 1,2-dihydro-4(3H)-quinazolinone derivatives obtained in high yields by the reaction of new and commercially available aromatic aldehydes with anthranilic acid amides. A series of quinazolinone derivatives possessing anticancer and antiparasitic activities, as well as capable of preventing the progress of neurodegenerative diseases were characterized. There are grounds for clinical trials of these substances in order to select compounds being promising for clinical application.

An efficient route to vinyl substituted oxadiazoles and triazoles using phenylselanyl derivatives as precursor

Vinyl substituted oxadiazoles and triazoles were obtained from selenoxide syn-elimination of phenylselanylethyl substituted oxadiazoles and triazoles, which were prepared through hydrazinolysis, acylation, and cyclocondensation reactions of phenylselanyl-