138478-13-4

Basic information

• Product Name: isopropyl N-benzoylaziridine-2-carboxylate
• Synonyms: isopropyl N-benzoylaziridine-2-carboxylate
• CAS NO: 138478-13-4
• Molecular Weight: 233.267
• Mol File: 138478-13-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: isopropyl N-benzoylaziridine-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: isopropyl N-benzoylaziridine-2-carboxylate(138478-13-4)
• EPA Substance Registry System: isopropyl N-benzoylaziridine-2-carboxylate(138478-13-4)

Safety Data

• Hazardous Substances Data: 138478-13-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 5950-39-0 aziridine-2-carboxylic acid isopropyl ester 
• 68849-34-3 isopropyl α,β-dibromopropionate 

Downstream Products

• 138478-21-4 N-benzoyl-3,4-diisopropyloxycarbonyl-2-pyrrolidone 
• 139692-26-5 isopropyl 4-(benzoylamino)-2,3-diisopropyloxycarbonylbutanoate 
• 138478-16-7 isopropyl 2-(benzoylamino)-4,4-diisopropyloxycarbonylbutanoate 
• 138478-20-3 N-benzoyl-3-ethoxycarbonyl-4-isopropyloxycarbonyl-2-pyrrolidone 
• 138478-22-5 ethyl 4-(benzoylamino)-2,3-diethoxycarbonylbutanoate 
• 138478-18-9 ethyl 4-(benzoylamino)-2-ethoxycarbonyl-3-isopropyloxycarbonylbutanoate 
• 138478-15-6 ethyl 4-(benzoylamino)-2-ethoxycarbonyl-4-isopropyloxycarbonylbutanoate 
• 23012-16-0 2-phenyl-1,3-oxazole-4-carboxylic acid 
• 37592-54-4 isopropyl 2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylate 
• 138478-32-7 isopropyl 2-phenyl-4,5-dihydro-1,3-oxazole-5-carboxylate 
• 138478-19-0 N-benzoyl-3-methoxycarbonyl-4-isopropyloxycarbonyl-2-pyrrolidone 
• 138478-17-8 methyl 4-(benzoylamino)-3-isopropyloxycarbonyl-2-methoxycarbonylbutanoate 
• 138478-14-5 methyl 4-(benzoylamino)-4-isopropyloxycarbonyl-2-methoxycarbonylbutanoate 
• 138478-35-0 isopropyl 2-(benzoylaminomethyl)-3,3-dicyanopropanoate 

Relevant articles and documents

Preparation of new 2,4-disubstituted oxazoles from N-acylaziridines

The efficiency of the ring enlargement of 2-substituted N-acylaziridines to dihydrooxazoles followed by nickel peroxide oxidation to give 2,4-disubstituted oxazoles as a synthetic route is examined. Sodium iodide-promoted ring enlargements work well for N-acylaziridines bearing electron-donating 2-substituents. For N-acylaziridines bearing electron-withdrawing 2-substituents, the best results are obtained using acid-promoted rearrangement.