926310-13-6

Basic information

• Product Name: Butanamide, 4-azido-N-phenyl-
• CAS NO: 926310-13-6
• Molecular Formula: C10H12N4O
• Molecular Weight: 204.231
• Mol File: 926310-13-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Butanamide, 4-azido-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanamide, 4-azido-N-phenyl-(926310-13-6)
• EPA Substance Registry System: Butanamide, 4-azido-N-phenyl-(926310-13-6)

Safety Data

• Hazardous Substances Data: 926310-13-6(Hazardous Substances Data)

Upstream product

• 7661-15-6 4-bromobutanoic acid N-phenylamide 
• 13140-15-3 N-phenyl-3-butenamide 
• 62-53-3 aniline 
• 7578-45-2 N-phenyl-4-chlorobutyramide 
• 14468-88-3 4-azidobutanoyl chloride 

Downstream Products

• 223394-90-9 N-phenyl-tetramethylenediamine 
• 1262759-57-8 C₂₈H₂₄N₄O₅ 

Relevant articles and documents

Anti-Markovnikov Hydroazidation of Alkenes by Visible-Light Photoredox Catalysis

The anti-Markovnikov hydroazidation of alkenes has been accomplished under visible-light irradiation by using [Ir(dF(CF3)ppy)2(dtbbpy)]PF6 as the photocatalyst and trimethylsilyl azide as the azidating agent. The reactions were greatly facilitated by water, the beneficial effect of which can be attributed to its participation in the reaction as the hydrogen donor, as indicated by deuterium isotope experiments. The reactions proceed under solvent free conditions in the presence of water. 4-Dimethylaminopyridine also exhibited a beneficial effect on the reactions. The present method enabled hydroazidation of several types of unactivated alkenes with good yields and high regioselectivity.

New synthetic routes for N-substituted 1,n-diamines. II. Synthesis of selectively N-substituted tetra- and pentamethylenediamines from ω-alkanoic acid derivatives

A new approach for the synthesis of selectively N-substituted tetra- and pentamethylenediamines 1 (n = 4,5) is described. The method uses N-substituted ω-haloalkanamides 2 as precursors and involves the microwave-promoted conversion into ω-azidocarboxamides 3 and later the reduction of both azido and carboxamide groups with diborane.