38968-72-8

Basic information

• Product Name: N-phenyl-(4-methoxypheny)acetimidoyl chloride
• Synonyms: N-phenyl-(4-methoxypheny)acetimidoyl chloride
• CAS NO: 38968-72-8
• Molecular Weight: 245.708
• Mol File: 38968-72-8.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: N-phenyl-(4-methoxypheny)acetimidoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyl-(4-methoxypheny)acetimidoyl chloride(38968-72-8)
• EPA Substance Registry System: N-phenyl-(4-methoxypheny)acetimidoyl chloride(38968-72-8)

Safety Data

• Hazardous Substances Data: 38968-72-8(Hazardous Substances Data)

Upstream product

• 7465-88-5 4-methoxy-N-phenylbenzamide 
• 100-07-2 4-methoxy-benzoyl chloride 
• 62-53-3 aniline 

Downstream Products

• 20800-30-0 (4-Methoxy-N-phenylbenzimidoyl)thioisocyanat 
• 1281680-98-5 3-(N-phenyl-4-methoxyphenylacetimidoyl)-1-(3-pyridylmethyl)thiourea 
• 1281680-99-6 1-(2-hydroxyethyl)-3-(N-phenyl-4-methoxyphenylacetimidoyl)thiourea 
• 1281681-00-2 1-ethoxycarbonylmethyl-3-(N-phenyl-4-methoxyphenylacetimidoyl)thiourea 
• 1281681-01-3 1-pentyl-3-(N-phenyl-4-methoxyphenylacetimidoyl)thiourea 
• 5784-95-2 2-(4-methoxyphenyl)-1H-indole 
• 1089303-32-1 4-methoxy-N-phenyl-benzimidic acid phenyl ester 
• 93663-77-5 4-hydroxy-2-(4-methoxy-phenyl)-quinoline-3-carboxylic acid ethyl ester 
• 25110-48-9 N,N'-diphenyl-4-methoxybenzamidine 
• 1609460-31-2 N-benzyl-4-methoxy-N′-phenylbenzimidamide 
• 56463-47-9 1-benzyl-2-(4-methoxyphenyl)-1H-benzo[d]imidazole 
• 84570-80-9 2-(4-methoxylphenyl)-4-phenylquinazoline 

Relevant articles and documents

Novel Conjugated s-Tetrazine Derivatives Bearing a 4H-1,2,4-Triazole Scaffold: Synthesis and Luminescent Properties

A series of new symmetrical s-tetrazine derivatives, coupled via a 1,4-phenylene linkage with a 4H-1,2,4-triazole ring, were obtained. The combination of these two rings in an extensively coupled system has significant potential applications, mainly in op

Silver(II) oxide-mediated synthesis of 2,4-diarylquinazolines

A single-pot procedure for the synthesis of 2,4-diarylquinazolines is described which involves a silver oxide-mediated C–H activation/C–N bond formation process. The generality of this method with respect to substituent effects is presented along with studies leading to process optimization. Mechanistic investigations provide support for the involvement of radical intermediates in the reaction process.

Transition Metal-Free Visible Light-Driven Photoredox Oxidative Annulation of Arylamidines

A fast catalytic synthesis of multisubstituted quinazolines from readily available amidines via visible light-mediated oxidative C(sp3)-C(sp2) bond formation has been established. This reaction is a metal-free oxidative coupling catalyzed by a photoredox organocatalyst. The protocol features low catalyst loading (1 mol %).