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 
• 123-62-6 propionic acid anhydride 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 79-05-0 Propionamid 
• 39800-84-5 propamidine 
• 64-19-7 acetic acid 
• 107-12-0 propiononitrile 
• 26728-51-8 sodium diacetamide 
• 74-88-4 methyl iodide 
• 5331-48-6 n-propylacetamide 
• 73895-07-5 N-Propionyl-acetamide; compound with GENERIC INORGANIC NEUTRAL COMPONENT 
• 157098-04-9 3-bromo-3-penten-2-one oxime 

Downstream Products

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

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.

Synthesis of 1,3,5-trisubstituted-1,2,4-triazoles by microwave-assisted N-acylation of amide derivatives and the consecutive reaction with hydrazine hydrochlorides

Facile and efficient procedures for the N-acylation reaction of amide derivatives with various acid anhydrides and the cyclization reaction of N-acylated amide derivatives with various hydrazine hydrochlorides were described. The reactions were carried out under microwave irradiation to give products in good yields in a few minutes. The synthesis of 1,3,5-trisubstituted- 1,2,4-triazoles from benzamides can also be accomplished in a simple one-pot sequential reaction.

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.