13324-82-8

Basic information

• Product Name: 4(1H)-Quinazolinone, 2,3-dihydro-2-[(1E)-2-phenylethenyl]-
• CAS NO: 13324-82-8
• Molecular Formula: C16H14N2O
• Molecular Weight: 250.3
• Mol File: 13324-82-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4(1H)-Quinazolinone, 2,3-dihydro-2-[(1E)-2-phenylethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 4(1H)-Quinazolinone, 2,3-dihydro-2-[(1E)-2-phenylethenyl]-(13324-82-8)
• EPA Substance Registry System: 4(1H)-Quinazolinone, 2,3-dihydro-2-[(1E)-2-phenylethenyl]-(13324-82-8)

Safety Data

• Hazardous Substances Data: 13324-82-8(Hazardous Substances Data)

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 28144-70-9 anthranilic acid amide 
• 610-15-1 2-nitrobenzamide 
• 118-48-9 isatoic anhydride 
• 101350-27-0 2-[(E)-3-phenylpropen-2-ylideneamino]benzamide 

Relevant articles and documents

One-pot B(C6F5)3 catalyzed cascade synthesis of 2-substituted-2,3-dihydroquinazolin-4(1H)-ones

A new and efficient B(C6F5)3 catalyzed domino strategy has been developed for the synthesis of 2-substituted quinazolinones. The reaction utilizes 2-aminobenzamide and aldehydes for a one-pot protocol. A wide range of substrate scope, functional group tolerance, and operational simplicity with excellent yield are synthetically useful features.

Efficient one-pot synthesis of 2,3-dihydroquinazoline-4(1H)-ones promoted by FeCl3/neutral Al2O3

2,3-Dihydroquinazolin-4(1H)-one derivatives have been synthesized via one-pot reaction of isatoic anhydride, aromatic aldehyde, and ammonium acetate catalyzed by FeCl3/neutral Al2O3 in tert-butanol under reflux conditions.

Tandem supramolecular synthesis of substituted 2-aryl-2,3- dihydroquinazolin-4(1H)-ones in the presence of β-cyclodextrin in water

Substituted 2-aryl-2,3-dihydroquinazolin-4(1H)-ones were prepared for the first time in water under neutral conditions by the reaction of aniline, isatoic anhydride, and aldehyde mediated by β-cyclodextrin in good yields. β-Cyclodextrin can be recovered a