134029-84-8

Basic information

• Product Name: N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide
• Synonyms: 4-Methoxy-N-(3,5-dimethoxyphenyl)benzamide;N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide
• CAS NO: 134029-84-8
• Molecular Formula: C₁₆H₁₇NO₄
• Molecular Weight: 287.31048
• Mol File: 134029-84-8.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide(134029-84-8)
• EPA Substance Registry System: N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide(134029-84-8)

Safety Data

• Hazardous Substances Data: 134029-84-8(Hazardous Substances Data)

Usage

Description

N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide is a chemical compound with the molecular formula C17H19NO4. It belongs to the class of benzamide derivatives and consists of a benzene ring with two methoxy groups at the 3 and 5 positions, and an amide group at the 4 position. N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide is commonly used in medicinal and pharmaceutical research for its potential therapeutic properties.

Uses

Used in Pharmaceutical Research:
N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide is used as a research compound for its potential therapeutic properties. It has been studied for its potential as an anti-inflammatory, anti-cancer, and analgesic agent.
Used in Drug Discovery:
N-(3,5-Dimethoxyphenyl)-4-methoxybenzamide is a promising compound for further research and development in the field of medicine and drug discovery. Its unique structure and potential therapeutic properties make it a valuable candidate for the development of new drugs and treatments.

Upstream product

• 100-07-2 4-methoxy-benzoyl chloride 
• 10272-07-8 3.5-dimethoxyaniline 
• 77-78-1 dimethyl sulfate 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 201230-82-2 carbon monoxide 
• 20734-67-2 3,5-dihydroxyphenylamine 
• 17213-58-0 3,5-dimethoxybenzamide 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 

Downstream Products

• 134054-81-2 N-(4-methoxybenzyl)-3,5-dimethoxybenzeneamine 
• 305834-44-0 N-(3,5-dimethoxy-2-methoxyacetyl-phenyl)-4-methoxy-benzamide 
• 305834-51-9 3,5,7-trimethoxy-2-(4-methoxy-phenyl)-1H-quinolin-4-one 
• 860233-40-5 5,7-dimethoxy-2-(4-methoxyphenyl)-1,4-dihydro-4-quinolinone 

Relevant articles and documents

Synthesis of dimethoxy activated benzimidazoles and bisbenzimidazoles

A range of 2-substituted-4,6-dimethoxy activated benzimidazoles and 2,2'-bisbenzimidazoles have been synthesized from 2-aminoanilide derivatives under acidic conditions. The starting materials were prepared either by acylation from 3,5-dimethoxyaniline followed by nitration, or by acylation from 3,5-dimethoxy-2-nitroaniline. The 2-nitroanilides were then reduced by palladium catalyzed reaction with hydrazine and subsequent acid catalyzed cyclization giving the corresponding 4,6-dimethoxybenzimidazoles and 4,6-dimethoxy-2,2'-bisbenzimidazoles. In addition, 2-phenyl-4,5,6-trimethoxybenzimidazole has been synthesized using a similar procedure.

Synthesis of heterocycle-based analogs of resveratrol and their antitumor and vasorelaxing properties

New resveratrol (RES) analogs were developed by replacing the aromatic 'core' of our initial naphthalene-based RES analogs with pseudo-heterocyclic (salicylaldoxime) or heterocyclic (benzofuran, quinoline, and benzothiazole) scaffolds. The resulting analo

A convenient method for the synthesis of 3,5,7-trimethoxy-2-phenyl-4-quinolones

The synthesis of 2-aryl-3,5,7-trimethoxy-4-quinolones was accomplished in three steps starting from 3,5-dimethoxyaniline and an aroyl chloride. These structures might be used as potential flavonol analogs. (C) 2000 Elsevier Science Ltd.