156747-40-9

Basic information

• Product Name: Benzamide, N-(2-aminopropyl)-
• Synonyms: Benzamide, N-(2-aminopropyl)-
• CAS NO: 156747-40-9
• Molecular Formula: C₁₀H₁₄N₂O
• Molecular Weight: 178.23
• Mol File: 156747-40-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzamide, N-(2-aminopropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(2-aminopropyl)-(156747-40-9)
• EPA Substance Registry System: Benzamide, N-(2-aminopropyl)-(156747-40-9)

Safety Data

• Hazardous Substances Data: 156747-40-9(Hazardous Substances Data)

Upstream product

• 19264-68-7 9-benzoyl-9H-carbazole 
• 78-90-0 1,2-diaminopropan 
• 98-88-4 benzoyl chloride 
• 7007-15-0 3-benzoyl-1,3-oxazolidin-2-one 

Downstream Products

• 23054-66-2 N-(2-hydroxypropyl)benzamide 

Relevant articles and documents

N-acylcarbazole as a selective transamidation reagent

N-acylation reaction offers an opportunity to develop an efficient synthesis of amide group-containing molecules. We found that N-acyl carbazoles showed remarkable selectivity in transamidation. Sterically less hindered primary amines are selectively acylated with N-acyl carbazoles without any additives. Various functional groups such as alcohol, phenol, indole, and aniline moieties are tolerated under mild conditions. The synthetic utility was displayed in one-pot synthesis of an N-acyl polyamine natural product. The terminal amines of spermidine were selectively benzoylated with N-benzoyl carbazole, followed by acetylation reaction accomplished the total synthesis in a highly efficient manner.

Group IV-Metal-Catalyzed Aminolysis of N-Acyl-2-oxazolidinones: Applications to the Chemoselective and Enantioselective Carbonylation of Primary Alkylamines

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