97492-34-7

Upstream product

• 1711-05-3 m-anisoyl chloride 
• 104-94-9 4-methoxy-aniline 
• 766-85-8 3-methoxy-1-iodobenzene 
• 201230-82-2 carbon monoxide 

Downstream Products

• 156085-96-0 3-methoxy-N-(4-methoxyphenyl)benzothioamide 
• 828264-31-9 ethyl 3',6-dimethoxy-2-phenyl-4-quinolone-3-carboxylate 
• 828264-16-0 2-[(3-methoxy-phenyl)-(4-methoxy-phenylamino)-methylene]-malonic acid diethyl ester 
• 142648-16-6 6-Methoxy-2-(3-methoxy-phenyl)-benzothiazole 
• 319015-44-6 3-hydroxy-N-(4-hydroxyphenyl)benzamide 
• 1456883-17-2 N-(4-methoxyphenyl)-N'-phenyl-3-methoxybenzamidine 

Relevant academic research and scientific papers

Computational Mechanistic Study on the Nickel-Catalyzed C-H/N-H Oxidative Annulation of Aromatic Amides with Alkynes: The Role of the Nickel (0) Ate Complex

Density functional theory (DFT) was used to unveil intimate mechanistic insights on the monodentate-chelation system that is used in the Ni-catalyzed C-H/N-H oxidative annulation of aromatic amides with alkynes, a reaction that was originally reported by

Stable and Reusable Binaphthyl-Supported Palladium Catalyst for Aminocarbonylation of Aryl Iodides

A binaphthyl-supported Pd nanoparticles (Pd-BNP)-catalyzed aminocarbonylation of aryl iodides in the presence of carbon monoxide and amines for the synthesis of amides has been developed. This methodology provides an efficient route for the synthesis of a COX-2 enzyme inhibitor having anti-inflammatory activity.

Synthesis, antileishmanial activity and structure-activity relationship of 1-N-X-phenyl-3-N′-Y-phenyl-benzamidines

Two series of N,N′-diphenyl-benzamidines were synthesized as part of a study to search potential new drugs with antileishmanial activity. These compounds were obtained by anilides in PCl5 halogenation reaction with generation in situ of the cor

Substituted 2-phenyl-4-quinolone-3-carboxylic acid compounds and their use as antitumor agents

Substituted 2-phenyl-4-quinolone-3-carboxylic acid derivatives and their salts were synthesized. The results of preliminary screening revealed that these compounds are potent in killing solid tumor cancers.

Synthesis and biological relationships of 3′,6-substituted 2-phenyl-4-quinolone-3-carboxylic acid derivatives as antimitotic agents

As part of a continuing search for potential anticancer drug candidates in the 2-phenyl-4-quinolone series, 3′,6-substituted 2-phenyl-4-quinolone-3- carboxylic acid derivatives and their salts were synthesized and evaluated. Preliminary screening showed t