19857-47-7

Basic information

• Product Name: 4(3H)-Quinazolinone, 3-(4-bromophenyl)-2-phenyl-
• CAS NO: 19857-47-7
• Molecular Formula: C20H13BrN2O
• Molecular Weight: 377.24
• Mol File: 19857-47-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4(3H)-Quinazolinone, 3-(4-bromophenyl)-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4(3H)-Quinazolinone, 3-(4-bromophenyl)-2-phenyl-(19857-47-7)
• EPA Substance Registry System: 4(3H)-Quinazolinone, 3-(4-bromophenyl)-2-phenyl-(19857-47-7)

Safety Data

• Hazardous Substances Data: 19857-47-7(Hazardous Substances Data)

Upstream product

• 5344-90-1 2-Aminobenzyl alcohol 
• 106-40-1 4-bromo-aniline 
• 50735-55-2 2-amino-N-(4-bromophenyl)benzamide 
• 119072-55-8 tert-butylisonitrile 
• 98-80-6 phenylboronic acid 
• 610-14-0 2-nitrobenzyl chloride 
• 2385-26-4 N-(4-bromophenyl)-2-nitrobenzamide 
• 100-51-6 benzyl alcohol 
• 698-16-8 benzohydroximoyl chloride 
• 780-20-1 N-benzylidene-4-bromoaniline 
• 1437798-56-5 4-(4-bromophenyl)-3,5-diphenyl-4,5-dihydro-1,2,4-oxadiazole 
• 3084-52-4 2-phenyl-4H-1,3-benzoxazin-4-one 
• 98-88-4 benzoyl chloride 
• 118-92-3 anthranilic acid 

Relevant articles and documents

Palladium-Catalyzed Oxidative Three-Component Coupling of Anthranilamides with Isocyanides and Arylboronic Acids: Access to 2,3-Disubstituted Quinazolinones

A novel palladium-catalyzed oxidative three-component coupling of easily accessible N-substituted anthranilamides with isocyanides and arylboronic acids is achieved. This protocol offers an alternative approach toward 2,3-disubstituted quinazolinones with a wide substrate scope and good functional group tolerance.

Oxidative radical skeletal rearrangement induced by molecular oxygen: Synthesis of quinazolinones

Oxidative skeletal rearrangement of 5-aryl-4,5-dihydro-1,2,4-oxadiazoles into quinazolinones is induced by molecular oxygen (under a dry air atmosphere) that likely proceeds via transient iminyl radical species. Concise syntheses of biologically active qu

Reinvestigation of the synthesis of 2-benzyl-3-aryl-quinazolin-4-[3H]-ones. An improved multi-component procedure using microwaves

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