389572-79-6

Basic information

• Product Name: 2-Aziridinecarboxamide,N,N,3-trimethyl-,(2R,3S)-rel-(9CI)
• Synonyms: 2-Aziridinecarboxamide,N,N,3-trimethyl-,(2R,3S)-rel-(9CI)
• CAS NO: 389572-79-6
• Molecular Formula: C6H12N2O
• Molecular Weight: 128.17228
• Product Categories: AMINETERTIARY
• Mol File: 389572-79-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Aziridinecarboxamide,N,N,3-trimethyl-,(2R,3S)-rel-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Aziridinecarboxamide,N,N,3-trimethyl-,(2R,3S)-rel-(9CI)(389572-79-6)
• EPA Substance Registry System: 2-Aziridinecarboxamide,N,N,3-trimethyl-,(2R,3S)-rel-(9CI)(389572-79-6)

Safety Data

• Hazardous Substances Data: 389572-79-6(Hazardous Substances Data)

Upstream product

• 14064-75-6 (E)-N,N-dimethylcrotonamide 
• 185-79-5 3,3-pentamethylenediaziridine 

Relevant articles and documents

cis-selective aziridination of cis- or trans-α,β-unsaturated amides using diaziridine

Aziridination of αβ-unsaturated amides was effected by treatment with lithiated 3,3-pentamethylenediaziridine in high diastereoselectivity, cis- Aziridine was the predominant diastereomer irrespective of the geometry of the substrates. A stepwise mechanis

Highly diastereoselective aziridination of α,β-unsaturated amides using diaziridine

Racemic 3-cyclohexyl-1-methyldiaziridine was found to react with α,β-unsaturated amides in basic conditions, giving N-unprotected trans-aziridines, while 3,3-pentamethylenediaziridine had been reported to afford cis-aziridines in high diastereoselectivity