82912-42-3

Basic information

• Product Name: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI)
• Synonyms: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI);tert-butyl aziridine-2-carboxylate
• CAS NO: 82912-42-3
• Molecular Formula: C7H13NO2
• Molecular Weight: 143.18
• Product Categories: CARBOXYLICESTER
• Mol File: 82912-42-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 66 °C(Press: 12 Torr)
• Appearance: /
• Density: 1.049±0.06 g/cm3(Predicted)
• PKA: 5.76±0.40(Predicted)
• CAS DataBase Reference: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI)(82912-42-3)
• EPA Substance Registry System: 2-Aziridinecarboxylicacid,1,1-dimethylethylester(9CI)(82912-42-3)

Safety Data

• Hazardous Substances Data: 82912-42-3(Hazardous Substances Data)

Upstream product

• 360-89-4 octafluoro-2-butene 
• 82912-35-4 N-Trimethylsilyl-2-(t-butoxycarbonyl)-aziridine 
• 138034-79-4 tert-butyl 2,3-dibromopropionate 
• 1663-39-4 tert-Butyl acrylate 
• 5950-34-5 methyl aziridine-2-carboxylate 
• 75-65-0 tert-butyl alcohol 

Relevant articles and documents

Acyl migration from N to C in aziridine-2-carboxylic esters

Acyl group migration from N to C in aziridine-2-carboxylates takes place in deprotonation reactions and, as a result, aziridine-2,2-dicarboxylates are formed. Mechanistic studies proved that the observed migration is an intramolecular reaction.

Unnatural amino acids. 2. Simple method of obtaining esters of aziridine-2-carboxylic acids by a transesterification reaction

A series of N-unsubstituted esters of aziridine-2-carboxylic acid has been obtained by transesterification in basic medium using primary, secondary, and tertiary alcohols. Methods of transesterification using various bases (K 2CO3, R

Synthesis of 3,4-Bis-1H-pyrrole

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