60692-36-6

Basic information

• Product Name: 2-benzoyl-1-benzylaziridine
• Synonyms: 2-benzoyl-1-benzylaziridine
• CAS NO: 60692-36-6
• Molecular Weight: 237.301
• Mol File: 60692-36-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-benzoyl-1-benzylaziridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzoyl-1-benzylaziridine(60692-36-6)
• EPA Substance Registry System: 2-benzoyl-1-benzylaziridine(60692-36-6)

Safety Data

• Hazardous Substances Data: 60692-36-6(Hazardous Substances Data)

Upstream product

• 1326628-20-9 1-benzyl-N-methoxy-N-methylaziridine-2-carboxamide 
• 100-58-3 phenylmagnesium bromide 
• 34943-06-1 1-benzylaziridine-2-carboxylic acid ethyl ester 

Downstream Products

• 1309589-31-8 (1-benzyl-3,5-diphenyl-1H-pyrrol-2-yl)methanol 
• 1309589-32-9 (1-benzyl-5-(2-methoxyphenyl)-3-phenyl-1H-pyrrol-2-yl)methanol 
• 1309589-33-0 (1-benzyl-3-phenyl-5-(pyridin-2-yl)-1H-pyrrol-2-yl)methanol 
• 1309589-35-2 2-(azidomethyl)-1-benzyl-3,5-diphenyl-1H-pyrrole 
• 1309589-36-3 2-(azidomethyl)-1-benzyl-5-(2-methoxyphenyl)-3-phenyl-1H-pyrrole 
• 1309589-37-4 2-(5-(azidomethyl)-1-benzyl-4-phenyl-1H-pyrrol-2-yl)pyridine 
• 1309589-38-5 2-(azidomethyl)-1-benzyl-5-(4-methoxyphenyl)-3-phenyl-1H-pyrrole 
• 60692-40-2 1-benzyl-2-(1-phenylvinyl)aziridine 

Relevant articles and documents

Metal-free aza-Claisen type ring expansion of vinyl aziridines: An expeditious synthesis of seven membered N-heterocycles

A metal-free approach for the synthesis of 7-membered aza-heterocycles has been developed by the intermolecular [5 + 2] cycloaddition of non-activated vinylaziridines and alkynes. This method has a broad substrate scope under mild reaction conditions to a

Synthesis of 1,2,5- and 1,2,3,5-substituted pyrroles from substituted aziridines via Ag(I)-catalyzed intramolecular cyclization

An efficient synthesis of 1,2,5- and 1,2,3,5-substituted pyrroles has been achieved from the sequential reactions including a ring-opening of 1-(aziridin-2-yl)propargylic alcohols by various nucleophiles under mild condition followed by an intramolecular