87282-04-0

Basic information

• Product Name: 3,5-dimethoxy-N-phenylbenzamide
• Synonyms: 3,5-dimethoxy-N-phenylbenzamide
• CAS NO: 87282-04-0
• Molecular Formula: C₁₅H₁₅NO₃
• Molecular Weight: 257.2845
• Mol File: 87282-04-0.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,5-dimethoxy-N-phenylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dimethoxy-N-phenylbenzamide(87282-04-0)
• EPA Substance Registry System: 3,5-dimethoxy-N-phenylbenzamide(87282-04-0)

Safety Data

• Hazardous Substances Data: 87282-04-0(Hazardous Substances Data)

Upstream product

• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 62-53-3 aniline 
• 91-52-1 2,4 dimethoxybenzoic acid 
• 103-71-9 phenyl isocyanate 
• 64-10-8 phenyl carbamate 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 98-95-3 nitrobenzene 
• 591-50-4 iodobenzene 
• 17213-58-0 3,5-dimethoxybenzamide 
• 108-86-1 bromobenzene 
• 142-04-1 aniline hydrochloride 
• 17213-57-9 3,5-dimethoxybenzoyl chloride 
• 87281-99-0 3,5-Dimethoxy-N-phenyl-benzimidoyl chloride 

Downstream Products

• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 16909-11-8 3-(3,5-dimethoxyphenyl)acrylic acid 

Relevant articles and documents

Amide bond synthesis via silver(I) N-heterocyclic carbene-catalyzed and tert-butyl hydroperoxide-mediated oxidative coupling of alcohols with amines under base free conditions

We present a base free method for amide bond construction via oxidative coupling of alcohols with amines catalyzed by Silver(I) N-heterocyclic carbenes (Ag(I)-NHCs) and mediated by tert-butyl hydroperoxide (TBHP) in ethanol. The results of controlled experiments suggest that the oxidative coupling proceeds through the formation of aldehyde, then subsequent attack by amine to give hemiaminal, which can then be oxidized to amide.

Ru(II)-catalyzed ortho-amidation and decarboxylation of aromatic acids: A versatile route to meta-substituted N-aryl benzamides

Carboxylate as a promising and valuable directing group has attracted a great deal of attention. However, employing it as a traceless direction group has rarely been reported. We developed the ruthenium-catalyzed amidation of substituted benzoic acids wit

A convenient synthesis of N-aryl benzamides by rhodium-catalyzed ortho-amidation and decarboxylation of benzoic acids

The rhodium-catalyzed amidation of substituted benzoic acids with isocyanates by directed C-H functionalization followed by decarboxylation to afford the corresponding N-aryl benzamides is demonstrated, in which the carboxylate serves as a unique, removable directing group. Notably, less common meta-substituted N-aryl benzamides are generated readily from more accessible paraor ortho-substituted groups by employing this strategy.