7473-90-7

Basic information

• Product Name: N-butyrylbenzamide
• Synonyms: N-butyrylbenzamide;N-Butanoylbenzamide
• CAS NO: 7473-90-7
• Molecular Formula: C₁₁H₁₃NO₂
• Molecular Weight: 0
• Mol File: 7473-90-7.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 337.1°C at 760 mmHg
• Flash Point: 140.9°C
• Appearance: /
• Density: 1.083g/cm³
• Vapor Pressure: 0.000107mmHg at 25°C
• Refractive Index: 1.521
• CAS DataBase Reference: N-butyrylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-butyrylbenzamide(7473-90-7)
• EPA Substance Registry System: N-butyrylbenzamide(7473-90-7)

Safety Data

• Hazardous Substances Data: 7473-90-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H13NO2/c1-2-6-10(13)12-11(14)9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3,(H,12,13,14)

Upstream product

• 33243-87-7 N-butyryl-benzimidic acid ethyl ester 
• 106-31-0 butanoic acid anhydride 
• 55-21-0 benzamide 
• 141-75-3 butyryl chloride 
• 97485-16-0 4-Phenyl-2-propyl-4H-oxazol-5-one 
• 51767-61-4 (E,Z)-2-phenyl-4-propylidene-4,5-dihydrooxazol-5-one 
• 2782-40-3 N-butylbenzamide 
• 82734-96-1 butyryl-α-phenylglycine 
• 825-60-5 benzimidic acid ethyl ester 
• 2432-51-1 ethylthioacetic acid methyl ester 
• 541-35-5 butanamide 
• 100-52-7 benzaldehyde 
• 100-47-0 benzonitrile 
• 163685-98-1 N-phenylbutyrimidamide 

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.

N-Butylammonium carboxylates/Tf2O: Ionic liquid based systems for the synthesis of unsymmetrical imides via a Ritter-type reaction

We have developed a new method for the preparation of unsymmetrical imides using liquid carboxylate salts via a Ritter-type process. The reactions were carried out with nitriles and n-butylammonium carboxylates as ionic liquids in the presence of triflic anhydride (Tf2O) as the promoter. Mild reaction conditions, simplicity of the procedure, and proton-free conditions are the main advantages of this procedure.

Highly efficient copper-catalyzed amidation of aldehydes by C-H activation

We have developed a highly efficient method for the copper-catalyzed amidation of aldehydes in the presence of N-bromosuccinimide (NBS). This method is simple, economical, and has practical advantages for synthesis of imides.