19264-34-7

Basic information

• Product Name: N-Acetylpropionamide
• Synonyms: N-Acetylpropanamide;N-Acetylpropionamide
• CAS NO: 19264-34-7
• Molecular Formula: C₅H₉NO₂
• Molecular Weight: 115.13
• Mol File: 19264-34-7.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Acetylpropionamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Acetylpropionamide(19264-34-7)
• EPA Substance Registry System: N-Acetylpropionamide(19264-34-7)

Safety Data

• Hazardous Substances Data: 19264-34-7(Hazardous Substances Data)

Upstream product

• 60-35-5 acetamide 
• 79-03-8 propionyl chloride 
• 73895-07-5 N-Propionyl-acetamide; compound with GENERIC INORGANIC NEUTRAL COMPONENT 
• 123-62-6 propionic acid anhydride 
• 75-05-8 acetonitrile 
• 79-16-3 N-methyl-acetamide 
• 108-24-7 acetic anhydride 
• 107-12-0 propiononitrile 
• 623-59-6 N-acetyl-N'-methylurea 
• 78-95-5 chloroacetone 
• 79-05-0 Propionamid 
• 157098-04-9 3-bromo-3-penten-2-one oxime 
• 5331-48-6 n-propylacetamide 
• 26728-51-8 sodium diacetamide 

Downstream Products

• 131214-21-6 (E)-2-methyl-3-phenylacrylamide 
• 463-51-4 Ketene 
• 79-05-0 Propionamid 
• 60-35-5 acetamide 
• 141-78-6 ethyl acetate 
• 105-37-3 Ethyl propionate 
• 6050-26-6 dipropionamide 
• 625-77-4 N-acetylacetamide 
• 84050-60-2 2-methyl-3-(2-furyl)-propenoic acid 
• 539-47-9 3-(fur-2-yl)crotonic acid 
• 2116-41-8 1-Acetyl-1-phenylhydrazin 

Relevant articles and documents

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.

Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent-free conditions

A rapid and convenient preparation of acyclic imides by the reaction of aliphatic and aromatic nitriles with acyclic carboxylic anhydride in the presence of catalytic amounts of p-toluenesulfonic acid under thermal or ultrasonic conditions is reported. The advantages of this procedure are moderate reaction times, good to excellent yields, and use of an inexpensive and ecofriendly catalyst. The reaction of nitriles with aliphatic anhydrides proceeds under thermal conditions, while they are accelerated by the use of ultrasound irradiation.

A novel one-pot synthesis of unsymmetrical acyclic imides

A new and convenient method was found for the one-pot synthesis of symmetrical and unsymmetrical linear imides by reaction of aliphatic and aromatic nitriles with acyclic carboxylic anhydrides in the presence of silica sulfuric acid as an active and recyclable reagent. Georg Thieme Verlag Stuttgart.