1522-67-4

Basic information

• Product Name: 3,4-DIMETHOXYBENZANILIDE
• Synonyms: 3,4-DIMETHOXYBENZANILIDE;3,4-dimethoxy-N-phenylbenzamide
• CAS NO: 1522-67-4
• Molecular Formula: C₁₅H₁₅NO₃
• Molecular Weight: 257.28
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 1522-67-4.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3,4-DIMETHOXYBENZANILIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIMETHOXYBENZANILIDE(1522-67-4)
• EPA Substance Registry System: 3,4-DIMETHOXYBENZANILIDE(1522-67-4)

Safety Data

• Hazardous Substances Data: 1522-67-4(Hazardous Substances Data)

Usage

General Description

3,4-DIMETHOXYBENZANILIDE is a chemical compound with the molecular formula C15H15NO3. It is a derivative of anilide, a class of compounds with a phenyl group attached to an amide functional group. This particular compound has two methoxy groups attached to the benzene ring at the 3 and 4 positions. 3,4-DIMETHOXYBENZANILIDE is commonly used in organic synthesis as a building block for various pharmaceuticals and agrochemicals. It has also been studied for its potential pharmacological properties, including its antiviral and analgesic effects. However, its exact mechanisms of action and potential applications are still under investigation.

Upstream product

• 186581-53-3 diazomethane 
• 52189-58-9 3,4-dihydroxy-benzoic acid anilide 
• 62-53-3 aniline 
• 3535-37-3 3,4-dimethoxybenzoic acid chloride 
• 27895-67-6 N-(3,4-dimethoxybenzylidene)aniline 
• 93-07-2 Veratric acid 
• 105417-03-6 3,4-Dimethoxybenzophenone tosylhydrazone 
• 7553-56-2 iodine 
• 4038-14-6 3,4-dimethoxybenzophenone 
• 91-16-7 1,2-dimethoxybenzene 
• 103-72-0 phenyl isothiocyanate 
• 103-71-9 phenyl isocyanate 
• 122775-35-3 3,4-Dimethoxyphenylboronic acid 
• 701-73-5 methyl N-phenyldithiocarbamate 

Downstream Products

• 4741-58-6 4,5-dimethoxyisobenzofuran-1(3H)-one 
• 115802-61-4 N-phenyl-3,4-dimethoxy-2-(4'-methoxybenzyl)benzamide 
• 117671-67-7 4,5-dimethoxy-3-(4'-methoxyphenyl)phthalide 
• 115802-58-9 3,4-dimethoxy-2-(4'-methoxybenzyl)benzoic acid 
• 115888-85-2 (+/-)-latifine dimethyl ether 
• 115802-59-0 N-methyl-3,4-dimethoxy-2-(4'-methoxybenzyl)benzamide 
• 115802-60-3 5,6-dimethoxy-4-(4'-methoxyphenyl)-2-methylisoquinolin-1(2H)-one 
• 115831-71-5 3,4-dihydro-3-hydroxy-5,6-dimethoxy-4-(4'-methoxyphenyl)-2-methylisoquinolin-1(2H)-one 
• 106664-04-4 6,7-dimethoxy-2-phenylbenzo[d][1,2]selenazol-3(2H)-one 
• 92552-99-3 2-(3,4-dimethoxyphenyl)-1,3-benzoxazole 
• 1103414-83-0 N-(isoquinolin-1-yl)-3,4-dimethoxy-N-phenylbenzamide 
• 1620646-06-1 N-but-3-enyl-3,4-dimethoxy-N-phenyl-benzamide 
• 1620646-08-3 3,4-dimethoxy-N-pent-4-enyl-N-phenyl-benzamide 
• 1620646-07-2 3,4-dimethoxy-N-[(E)-5-oxopent-3-enyl]-N-phenyl-benzamide 

Relevant articles and documents

Studies on enamides. Part-5: A novel pathway for photochemical reaction of N-1-cyclohexenyl-N-phenylarylamides

The oxidative photolysis of N-1-cyclohexenyl-N-phenylarylamides has culminated in the photochemical synthesis of anilides by a novel reaction pathway.

Rhodium-Catalyzed Synthesis of Amides from Functionalized Blocked Isocyanates

Isocyanates are useful building blocks for the synthesis of amides, although their widespread use has been limited by their high reactivity, which often results in poor functional group tolerance and a propensity to oligomerize. Herein, a rhodium-catalyzed synthesis of amides is described coupling boroxines with blocked (masked) isocyanates. The success of the reaction hinges on the ability to form both the isocyanate and the organorhodium intermediates in situ. Relying on masked isocyanate precursors and on the high reactivity of the organorhodium intermediate results in broad functional group tolerance, including protic nucleophilic groups such as amines, anilines, and alcohols.

A metal-free and a solvent-free synthesis of thio-amides and amides: An efficient Friedel-Crafts arylation of isothiocyanates and isocyanates

A rapid, metal-free and solvent-free (very low loading of solvent in few cases) reaction conditions for synthesizing thioamides and amides using a Bronsted super acid such as triflic acid has been developed. This method shows a broad substrate scope with

Dithiocarbamate and DBU-promoted amide bond formation under microwave condition

Dithiocarbamate and DBU-promoted amide bond formation under microwave condition has been reported. The versatility of this synthetic protocol has been demonstrated with various carboxylic acids and different dithiocarbamates. The products thus obtained ha