1350616-38-4

Basic information

• Product Name: 3'-benzyl-1'H,2H-spiro[acenaphthylene-1,2'-quinazoline]-2,4'(3'H)-dione
• Synonyms: 3'-benzyl-1'H,2H-spiro[acenaphthylene-1,2'-quinazoline]-2,4'(3'H)-dione
• CAS NO: 1350616-38-4
• Molecular Weight: 390.441
• Mol File: 1350616-38-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3'-benzyl-1'H,2H-spiro[acenaphthylene-1,2'-quinazoline]-2,4'(3'H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-benzyl-1'H,2H-spiro[acenaphthylene-1,2'-quinazoline]-2,4'(3'H)-dione(1350616-38-4)
• EPA Substance Registry System: 3'-benzyl-1'H,2H-spiro[acenaphthylene-1,2'-quinazoline]-2,4'(3'H)-dione(1350616-38-4)

Safety Data

• Hazardous Substances Data: 1350616-38-4(Hazardous Substances Data)

Upstream product

• 52745-10-5 N-(phenylmethyl)-2-nitrobenzamide 
• 82-86-0 acenaphthene quinone 
• 5471-20-5 2-amino-N-benzylbenzamide 

Relevant articles and documents

Structurally diversified synthesis of 2,3-dihydroquinazolin-4-(1H)-ones from 2-aminobenzamides and 1,2-dicarbonyl compounds in ionic liquids catalyzed by iodine

Abstract: A green procedure for the rapid diversification of quinazolin-4-(1H)-one scaffolds is described in this paper. Various types of 1,2-dicarbonyl compounds are treated with 2-aminobenzamides in ionic liquids catalyzed by iodine and unexpectedly afford structurally diversified single-quinazoline derivatives. The recyclability of the ionic liquids makes this protocol to be an environmentally benign procedure. Graphical Abstract: A total of 39 quinazolin-4-(1H)-one scaffolds were synthesized via a green procedure of 1,2-dicarbonyl compounds and 2-aminobenzamides in ionic liquids catalyzed by iodine.[Figure not available: see fulltext.]