197020-64-7

Basic information

• Product Name: (+/-)-(N-tert-Butoxycarbonyl)-2-phenylaziridine
• Synonyms: (+/-)-(N-tert-Butoxycarbonyl)-2-phenylaziridine
• CAS NO: 197020-64-7
• Molecular Weight: 219.283
• Mol File: 197020-64-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (+/-)-(N-tert-Butoxycarbonyl)-2-phenylaziridine(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-(N-tert-Butoxycarbonyl)-2-phenylaziridine(197020-64-7)
• EPA Substance Registry System: (+/-)-(N-tert-Butoxycarbonyl)-2-phenylaziridine(197020-64-7)

Safety Data

• Hazardous Substances Data: 197020-64-7(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 150884-56-3 N-tert-butyloxycarbonyl-3-(4-cyanophenyl)oxaziridine 
• 462100-44-3 oxaziridine-2,3,3-tricarboxylic acid 2-tert-butyl ester 3,3-diethyl ester 
• 20989-17-7 Phenylglycinol 
• 102089-74-7 tert-butyl 2-hydroxy-1-phenylethylcarbamate 
• 7568-93-6 2-Amino-1-phenylethanol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 67341-07-5 tert-butyl N-(2-hydroxy-2-phenylethyl)carbamate 

Downstream Products

• 113525-79-4 2-Oxo-5-phenyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 182921-04-6 tert-butyl (2,2-diphenylethyl)carbamate 
• 7693-77-8 5-phenyloxazolidin-2-one 

Relevant articles and documents

Heteroatom transfer to alkenes by N-protected-oxaziridines: New reaction pathways and products

N-Alkoxycarbonyl- and N-carboxamido-oxaziridines are shown to react with aromatic alkenes to give epoxide, aziridine or hydro-oxidation products, in ratios depending on the oxaziridine structure. Chiral oxaziridines can effect epoxidation and hydro-oxidation with promising levels of asymmetric induction.

Enantioselective synthesis of β-hydroxy amines and aziridines using asymmetric transfer hydrogenation of α-amino ketones

Enantioselective transfer hydrogenation of α-amino ketones is an effective method for the asymmetric synthesis of β-hydroxy amines and aziridines.