130250-62-3

Basic information

• Product Name: 2,N-DIMETHOXY-N-METHYLBENZAMIDE
• Synonyms: 2,N-DIMETHOXY-N-METHYLBENZAMIDE;N-2-DiMethoxy-N-MethylbenzaMide;2-Methoxy-N-Methoxy-N-MethylbenzaMide
• CAS NO: 130250-62-3
• Molecular Formula: C₁₀H₁₃NO₃
• Molecular Weight: 195.22
• Mol File: 130250-62-3.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,N-DIMETHOXY-N-METHYLBENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,N-DIMETHOXY-N-METHYLBENZAMIDE(130250-62-3)
• EPA Substance Registry System: 2,N-DIMETHOXY-N-METHYLBENZAMIDE(130250-62-3)

Safety Data

• Hazardous Substances Data: 130250-62-3(Hazardous Substances Data)

Usage

General Description

2,N-DIMETHOXY-N-METHYLBENZAMIDE is a chemical compound that is commonly used as a building block in organic synthesis and pharmaceutical research. It is a substituted benzamide derivative with two methoxy groups on the phenyl ring and a methyl group attached to the amide nitrogen. 2,N-DIMETHOXY-N-METHYLBENZAMIDE has the potential to be used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It has been studied for its potential biological activities and has shown promise as a potential drug candidate in some research studies. Additionally, it is used in various chemical reactions as a reagent and has also been investigated for its potential use in material science and polymer chemistry.

Upstream product

• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 579-75-9 2-Methoxybenzoic acid 
• 21615-34-9 2-Methoxybenzoyl chloride 
• 1117-97-1 N,0-dimethylhydroxylamine 
• 578-57-4 2-bromoanisole 
• 201230-82-2 carbon monoxide 
• 30289-28-2 N-methoxy-N-methylcarbamoyl chloride 
• 612-16-8 (2-methoxyphenyl)methanol 

Downstream Products

• 2491-31-8 2-hydroxy-deoxybenzoin 
• 574-12-9 isoflavone 
• 7622-32-4 2'-Methoxyisoflavone 
• 33470-10-9 1-(2-methoxyphenyl)-2-phenylethanone 
• 66659-59-4 1-(2-methoxyphenyl)-2-(2-methoxyphenyl)ethanone 
• 55169-98-7 2’-methoxy-3’,5’-dimethylacetophenone 
• 1443986-43-3 2-bromo-2-(3-bromophenyl)-1-(2-methoxyphenyl)ethanone 
• 1443986-46-6 3-(3-bromophenyl)-2-(2-methoxyphenyl)-6-(thien-3-yl)imidazo[1,2-b]pyridazine 
• 1443986-16-0 3-(2'-hydroxybiphenyl-3-yl)-2-(2-methoxyphenyl)-6-(thien-3-yl)imidazo[1,2-b]pyridazine 

Relevant articles and documents

Biocatalytic Strategy for the Highly Stereoselective Synthesis of CHF2-Containing Trisubstituted Cyclopropanes

The difluoromethyl (CHF2) group has attracted significant attention in drug discovery and development efforts, owing to its ability to serve as fluorinated bioisostere of methyl, hydroxyl, and thiol groups. Herein, we report an efficient biocat

An efficient and versatile synthesis of isoflavones from 2-methoxybenzoic acids

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Copper-catalyzed synthesis of weinreb amides by oxidative amidation of alcohols

A simple and efficient protocol has been developed for the oxidative amidation of alcohols to Weinreb amides using tert-butyl hydroperoxide as an oxidant and an inexpensive and air stable copper catalyst. The present protocol is advantageous as it uses commercially affordable alcohols as starting materials. The developed protocol also tolerates various substituted alcohols as starting materials to provide good to excellent yields of the desired products.