52379-48-3

Basic information

• Product Name: Benzenecarboximidamide, 4-(dimethylamino)-N-phenyl-
• CAS NO: 52379-48-3
• Molecular Formula: C15H17N3
• Molecular Weight: 239.32
• Mol File: 52379-48-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidamide, 4-(dimethylamino)-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidamide, 4-(dimethylamino)-N-phenyl-(52379-48-3)
• EPA Substance Registry System: Benzenecarboximidamide, 4-(dimethylamino)-N-phenyl-(52379-48-3)

Safety Data

• Hazardous Substances Data: 52379-48-3(Hazardous Substances Data)

Upstream product

• 6083-47-2 4-(dimethylamino)benzamide 
• 62-53-3 aniline 
• 1197-19-9 4-cyano-N,N-dimethylaniline 
• 2829-28-9 4-dimethylamino-benzaldehyde phenylhydrazone 

Downstream Products

• 15030-24-7 2-(4-(dimethylamino)phenyl)-1-phenyl-1H-naphtho[2,3-d]imidazole-4,9-dione 
• 1350629-10-5 1-phenyl-2-(4-N,N-dimethylamino-phenyl)-1H-imidazo[4,5-b]pyrazine 
• 1350629-13-8 1-phenyl-2-(4-N,N-dimethylamino-phenyl)-1H-imidazo[4,5-b]quinoxaline 
• 1350629-01-4 1-phenyl-2-(4-N,N-dimethylamino-phenyl)-1H-5-methoxy-benzo[d]imidazole 
• 2562-73-4 1-phenyl-2-(4-N,N-dimethylamino-phenyl)-1H-benzo[d]imidazole 

Relevant articles and documents

Direct Synthesis of 3-Acylindoles through Rhodium(III)-Catalyzed Annulation of N-Phenylamidines with α-Cl Ketones

In the present study, a novel synthetic strategy to directly produce versatile 3-acylindoles through Rh(III)-catalyzed C-H activation and annulation cascade of N-phenylamidines with α-Cl ketones was developed, in which α-Cl ketones serve as unusual one-carbon (sp3) synthons. This strategy features high regioselectivity, efficiency, wide substrate tolerance, and mild reaction conditions, which further underscore its synthetic utility in drug molecule synthesis.