7012-92-2

Basic information

• Product Name: 3-benzyl-6-chloro-2-phenylquinazolin-4(3H)-one
• Synonyms: 3-benzyl-6-chloro-2-phenylquinazolin-4(3H)-one
• CAS NO: 7012-92-2
• Molecular Weight: 346.816
• Mol File: 7012-92-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-benzyl-6-chloro-2-phenylquinazolin-4(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-benzyl-6-chloro-2-phenylquinazolin-4(3H)-one(7012-92-2)
• EPA Substance Registry System: 3-benzyl-6-chloro-2-phenylquinazolin-4(3H)-one(7012-92-2)

Safety Data

• Hazardous Substances Data: 7012-92-2(Hazardous Substances Data)

Upstream product

• 635-21-2 5-chloroanthranilic acid 
• 4743-17-3 5-Chloroisatoic anhydride 
• 100-46-9 benzylamine 
• 1508262-42-7 N-benzyl-4-chloro-N-(phenyl((pivaloyloxy)imino)methyl)benzamide 
• 698-16-8 benzohydroximoyl chloride 
• 1508262-91-6 N-benzyl-N'-(pivaloyloxy)benzimidamide 
• 3488-55-9 N-hydroxy-N'-(phenylmethyl)-benzenecarboximidamide 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 1666-17-7 benzaldehyde p-toluenesulfonylhydrazone 
• 958-77-0 6-chloro-2-phenyl-2,3-dihydroquinazolin-4(1H)-one 
• 591-50-4 iodobenzene 
• 24585-93-1 3-benzyl-6-chloroquinazolin-4(3H)-one 

Relevant articles and documents

One pot synthesis of some new N-allyl and N-benzyl quinazolinones and their anti-inflammatory activity

The simple and more reliable one-pot synthesis of some novel compounds of allyl/Benzyl quinazolinone (4aa-4bd) with good yields from readily available derivatives of anthranilic acid and benzoyl chloride was also reported. Interestingly, as compared to Di

Rhodium(II)-Catalyzed Carbenoid Insertion of N-Tosylhydrazones into Amide N-H Bonds: An Efficient Approach to N3-Benzyl/Alkyl-2-arylquinazolinones

Dirhodium(II) acetate-catalyzed reactions of N-tosylhydrazones with dihydroquinazolinones bearing different types of N-H bonds that give N3-benzyl/alkyl-2-arylquinazolin-4(3H)-ones through Csp3-N bond formation by oxidative dehydroge

Copper-catalyzed redox-neutral C-H amination with amidoximes

CuI-catalyzed reactions of N-alkylamidoximes afforded dihydroimidazoles via sp3 C-H amination. On the other hand, the reactions of N-benzoylamidoximes resulted in sp2 C-H amination to form quinazolinones. The reaction mechanisms could be characterized as a redox-neutral radical pathway including a Cu(i)-Cu(ii) redox catalytic cycle. The Royal Society of Chemistry.