73894-89-0

Basic information

• Product Name: Benzamide, N-acetyl-4-methoxy-
• Synonyms: Acetyl-(4-methoxy-benzoyl)-amin;Benzamide,N-acetyl-4-methoxy;acetyl-p-methoxybenzoylimide;acetyl-(4-methoxy-benzoyl)-amine
• CAS NO: 73894-89-0
• Molecular Formula: C10H11NO3
• Molecular Weight: 193.202
• Mol File: 73894-89-0.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Benzamide, N-acetyl-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-acetyl-4-methoxy-(73894-89-0)
• EPA Substance Registry System: Benzamide, N-acetyl-4-methoxy-(73894-89-0)

Safety Data

• Hazardous Substances Data: 73894-89-0(Hazardous Substances Data)

Upstream product

• 60-35-5 acetamide 
• 100-07-2 4-methoxy-benzoyl chloride 
• 99553-79-4 2-(4-methoxyphenyl)-4-methyl-5-oxo-4,5-dihydrooxazole 
• 3424-93-9 4-methoxyphenylacetamide 
• 108-24-7 acetic anhydride 
• 35103-34-5 N-(p-methoxybenzyl)acetamide 
• 2393-23-9 4-methoxy-benzylamine 
• 108462-96-0 DL-N-(4-methoxybenzoyl)alanine 
• 1147869-41-7 ethyl (2Z)-3-(acetylamino)-3-(4-methoxyphenyl)-2-phenylacrylate 
• 1147869-31-5 ethyl 2-diazo-3-hydroxy-3-(4-methoxyphenyl)-3-phenylpropanoate 
• 874-90-8 4-methoxybenzonitrile 
• 142-71-2 copper diacetate 
• 7403-41-0 N-ethyl-4-methoxy-benzamide 
• 100-09-4 4-methoxybenzoic acid 

Downstream Products

• 1211547-85-1 5-(4-methoxyphenyl)-3-methyl-1-phenyl-1H-1,2,4-triazole 

Relevant articles and documents

Method for catalytically oxidizing amine to be synthesized into amide through dipyridyl-type manganese catalyst

The invention discloses a methodfor catalytically oxidizing amine to be synthesized into amide througha dipyridyl-type manganese catalyst. According to the method, a dipyridyl manganese complex formedafter coordination of a dipyridyl-type complex and cheap metal manganese serves as the catalyst, clean and environment-friendly hydrogen peroxide serves as an oxidizing agent, oxidation of N ortho-position sp3 C-H bonds catalyzed by the cheap metal manganese is achieved, and the amine is directly oxidized to obtain the amide. Compared with existing methods, the method has the advantages that theadopted catalyst is low in price, the preparing method is simple, raw materials are easy to obtain, the use level of the catalyst is low, the substrate range is wide, the reaction condition is mild, the operation is simple and environmentally friendly, the reaction time is short, the yield is high, the selectivity is high, and the industrialization cost is low.

Visible-Light-Driven Oxidation of N -Alkylamides to Imides Using Oxone/H 2 O and Catalytic KBr

Imides are prepared conveniently by visible-light-driven oxidations of various N -alkylamides under mild conditions. The majority of the reactions proceed efficiently by using Oxone as the oxidant in the presence of a catalytic amount of KBr in H 2 O/CH 2 Cl 2 under irradiation by an 8 W white LED at room temperature. Experimental studies suggest that an imine, obtained from the substrate amide via a radical process, is the key intermediate.

Transition-Metal- and Halogen-Free Oxidation of Benzylic sp 3 C-H Bonds to Carbonyl Groups Using Potassium Persulfate

Aryl carbonyl compounds including acetophenones, benzophenones, imides, and benzoic acids are prepared from benzyl substrates using potassium persulfate as oxidant with catalytic pyridine in acetonitrile under mild conditions. Neither transition metals nor halogens are involved in the reactions.