58268-17-0

Basic information

• Product Name: Aziridine, 1-butyl-2,3-diphenyl-, (2R,3S)-rel-
• CAS NO: 58268-17-0
• Molecular Formula: C18H21N
• Molecular Weight: 251.371
• Mol File: 58268-17-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Aziridine, 1-butyl-2,3-diphenyl-, (2R,3S)-rel-(CAS DataBase Reference)
• NIST Chemistry Reference: Aziridine, 1-butyl-2,3-diphenyl-, (2R,3S)-rel-(58268-17-0)
• EPA Substance Registry System: Aziridine, 1-butyl-2,3-diphenyl-, (2R,3S)-rel-(58268-17-0)

Safety Data

• Hazardous Substances Data: 58268-17-0(Hazardous Substances Data)

Upstream product

• 908094-04-2 phenyldiazomethane 
• 1077-18-5 N-benzylidenebutan-1-amine 
• 100-52-7 benzaldehyde 
• 57527-55-6 (E)-N-benzylidenebutan-1-amine 

Downstream Products

• 100-52-7 benzaldehyde 
• 1077-18-5 N-benzylidenebutan-1-amine 
• 791-28-6 Triphenylphosphine oxide 
• 87964-46-3 4-n-butyl-3,5-diphenyl-1,2,4-dioxazolidine 
• 87964-46-3 4-n-butyl-3,5-diphenyl-1,2,4-dioxazolidine 
• 2782-40-3 N-butylbenzamide 
• 87964-46-3 (3S,5S)-4-Butyl-3,5-diphenyl-[1,2,4]dioxazolidine 

Relevant articles and documents

Aziridine synthesis in the presence of catalytic amounts of pyridiniums or viologens

Pyridinium and viologen species were found to induce an aziridine-forming reaction from various imines and phenyldiazomethane. The reactions were generally high yielding and demonstrated cis-aziridine selectivity.

[3+2] Cycloadditions and nucleophilic additions of aziridines under C-C and C-N bond cleavage

Under PET conditions (photoinduced electron transfer) aziridines react with dipolarophiles in a [3+2] cycloaddition to form five-membered heterocycles. In this study we used mono- and disubstituted N-alkyl and N-arylaziridines. We noticed that the radical