7291-00-1

Basic information

• Product Name: p-Methoxy-N,N-dimethylbenzamide
• Synonyms: N,N-Dimethyl-4-methoxybenzamide;N,N-Dimethyl-p-anisamide;p-Methoxy-N,N-dimethylbenzamide;4-Methoxy-N,N-dimethylbenzamide;Benzamide, 4-methoxy-N,N-dimethyl-;N,N-Dimethyl-p-methoxybenzamide;p-Anisamide, N,N-dimethyl-
• CAS NO: 7291-00-1
• Molecular Formula: C₁₀H₁₃NO₂
• Molecular Weight: 179.2157
• Mol File: 7291-00-1.mol
• Article Data: 59

Chemical Properties

• Boiling Point: 311.75°C (rough estimate)
• Flash Point: 144.6°C
• Appearance: /
• Density: 1.1248 (rough estimate)
• Vapor Pressure: 0.000438mmHg at 25°C
• Refractive Index: 1.5150 (estimate)
• CAS DataBase Reference: p-Methoxy-N,N-dimethylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: p-Methoxy-N,N-dimethylbenzamide(7291-00-1)
• EPA Substance Registry System: p-Methoxy-N,N-dimethylbenzamide(7291-00-1)

Safety Data

• Hazardous Substances Data: 7291-00-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H13NO2/c1-11(2)10(12)8-4-6-9(13-3)7-5-8/h4-7H,1-3H3

Upstream product

• 100-07-2 4-methoxy-benzoyl chloride 
• 124-40-3 dimethyl amine 
• 696-62-8 para-iodoanisole 
• 68-12-2 N,N-dimethyl-formamide 
• 506-59-2 N,N-dimethylammonium chloride 
• 121-98-2 methyl 4-methoxybenzoate 
• 104825-42-5 1,1-Bis-(4-methoxy-benzoyl)-3,3-dimethyl-urea 
• 106997-49-3 C₁₁H₁₆NO₅P 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 632-22-4 tetramethylurea 
• 623-12-1 4-chloromethoxybenzene 
• 18503-89-4 N,N-dimethylformamide diisopropyl acetal 
• 105-13-5 4-Methoxybenzyl alcohol 
• 92409-23-9 3-hydroxy-2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)propan-1-one 

Downstream Products

• 3400-22-4 4-methoxy-N-methylbenzamide 
• 15190-05-3 2-(dimethylamino)-2-(4-methoxyphenyl)acetonitrile 
• 1019388-59-0 2-hydroxy-4-methoxy-N,N-dimethylbenzamide 
• 1152-07-4 2-(4-methoxyphenyl)-3H-quinazolin-4-one 
• 6946-35-6 butyl 4-methoxybenzoate 
• 6265-92-5 2-(4-methoxy-phenyl)-benzothiazole 
• 838-34-6 2-(p-methoxyphenyl)benzoxazole 
• 2620-81-7 2-(4-methoxyphenyl)-1H-benzimidazole 
• 17428-96-5 1,1-d2-3-phenylpropan-1-ol 
• 15175-54-9 N,N-dimethyl-4-methoxylbenzylamine 
• 105-13-5 4-Methoxybenzyl alcohol 
• 19486-71-6 p-methoxybenzaldehyde-d1 
• 21875-72-9 1-(4-methoxy-phenyl)-2-phenylsulfanyl-ethanone 
• 93723-53-6 1-Dimethylamino-1-<4-methoxy-phenyl>-2-phenyl-aethan 

Relevant articles and documents

One-pot synthesis of a highly disperse core-shell CuO-alginate nanocomposite and the investigation of its antibacterial and catalytic properties

In this study, sodium alginate was extracted from Sargassum algae, collected from coastal waters of Bushehr, Persian Gulf, Iran and used as a stabilizing and wrapping agent for CuO nanoparticles. The synthesized nanocomposite was characterized by some spectroscopic and microscopic techniques, such as IR, XRD, Uv-vis, BET, BJH, zeta potential, SEM, TEM, HR-TEM, and XPS. The antibacterial effects of the CuO-alginate nanocomposite against some bacteria, isolated from a burn wound, were evaluated. The results showed that this nanocomposite had better antibacterial effects than its components onPseudomonas aeruginosaATCC 27853,Staphylococcus aureusATCC 12600,Streptococcus pyogenesATCC 19615, andStaphylococcus epidermidisATCC 49461. Among these,Staphylococcus aureusATCC 12600 was the most sensitive one to this nanocomposite, with the lowest minimum inhibitory concentration (2.08 mg mL?1) observed. Moreover, the synthesized nanocomposite showed good catalytic activity in the oxidative coupling of carboxylic acids withN,N-dialkylformamides toward the synthesis of amides.

Continuous Flow Acylation of (Hetero)aryllithiums with Polyfunctional N,N-Dimethylamides and Tetramethylurea in Toluene

The continuous flow reaction of various aryl or heteroaryl bromides in toluene in the presence of THF (1.0 equiv) with sec-BuLi (1.1 equiv) provided at 25 °C within 40 sec the corresponding aryllithiums which were acylated with various functionalized N,N-

Copper-Catalyzed Radical N-Demethylation of Amides Using N-Fluorobenzenesulfonimide as an Oxidant

An unprecedented N-demethylation of N-methyl amides has been developed by use of N-fluorobenzenesulfonimide as an oxidant with the aid of a copper catalyst. The conversion of amides to carbinolamines involves successive single-electron transfer, hydrogen-atom transfer, and hydrolysis, and is accompanied by formation of N-(phenylsulfonyl)benzenesulfonamide. Carbinolamines spontaneously decompose to N-demethylated amides and formaldehyde, because of their inherent instability.