72997-93-4

Basic information

• Product Name: 1-benzyl-2-benzoyl-3-phenylaziridine
• Synonyms: 1-benzyl-2-benzoyl-3-phenylaziridine
• CAS NO: 72997-93-4
• Molecular Weight: 313.399
• Mol File: 72997-93-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-benzyl-2-benzoyl-3-phenylaziridine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-2-benzoyl-3-phenylaziridine(72997-93-4)
• EPA Substance Registry System: 1-benzyl-2-benzoyl-3-phenylaziridine(72997-93-4)

Safety Data

• Hazardous Substances Data: 72997-93-4(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 64-17-5 ethanol 
• 72690-93-8 2,3-dichloro-1,3-diphenylpropan-1-one 
• 71-43-2 benzene 
• 60-29-7 diethyl ether 
• 32147-20-9 (Z)-2-bromo-1,3-diphenylprop-2-en-1-one 
• 3376-26-9 N-Benzylidenebenzylamine N-oxide 
• 536-74-3 phenylacetylene 
• 294886-74-1 N-benzyl-N-(1,3-diphenylprop-2-yn-1-yl)hydroxylamine 
• 294886-82-1 2-benzyl-3,5-diphenyl-2,3-dihydro-isoxazole 
• 3376-26-9 N-Benzylidenbenzylamin-N-oxid 
• 611-91-6 2,3-dibromo-1,3-diphenylpropane-1-one 
• 611-91-6 trans-2,3-dibromo-1,3-diphenylpropan-1-one 

Downstream Products

• 6628-56-4 (+/-)-benzyl-(1,3,5t-triphenyl-4,5-dihydro-1H-pyrazol-4r-yl)-amine 
• 2183-27-9 1,3,5-triphenyl-1H-pyrazole 
• 1258314-43-0 C₃₃H₂₉NO₂ 
• 1353722-06-1 benzyl 1-benzyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylate 
• 1353722-09-4 benzyl 1-benzyl-5-(1'-hydroxy-1'-phenylmethyl)-2-methyl-4-phenyl-1H-pyrrole-3-carboxylate 
• 1353722-08-3 benzyl 1-benzyl-2-ethyl-4-phenyl-1H-pyrrole-3-carboxylate 
• 1353722-07-2 benzyl 1,2-dibenzyl-4-phenyl-1H-pyrrole-3-carboxylate 
• 92-71-7 2,5-diphenyloxazole 
• 51220-12-3 1-benzyl-2-phenyl-1H-pyrrole-3,4-dicarboxylic acid dimethyl ester 
• 117835-94-6 ((2S,4R)-3-Benzyl-1,2-diphenyl-5-thioxo-imidazolidin-4-yl)-phenyl-methanone 
• 117835-90-2 1-Benzyl-5-[1-hydroxy-1-phenyl-meth-(E)-ylidene]-2,3-diphenyl-imidazolidin-4-one 
• 614-47-1 1,3-diphenyl-propen-3-one 

Relevant articles and documents

Synthesis of aziridines by electrochemical oxidative annulation of chalcones with primary amines

Synthesis of aziridines by electrochemical oxidative annulation of chalcone 1,3-diphenyl-2-propen-1-one with primary amines has been developed under external oxidant - and base-free conditions. The reaction constitutes a new transformation of chalcones with primary amines to aziridines, providing a complementary, simple, and environmentally friendly approach to the currently available methods. A reaction mechanism for this transformation has been proposed based on the cyclic voltammetry.

Oxygenation of Simple Olefins through Selective Allylic C?C Bond Cleavage: A Direct Approach to Cinnamyl Aldehydes

A novel metal-free allylic C?C σ-bond cleavage of simple olefins to give valuable cinnamyl aldehydes is reported. 1,2-Aryl or alkyl migration through allylic C?C bond cleavage occurs in this transformation, which is assisted by an alkyl azide reagent. This method enables O-atom incorporation into simple unfunctionalized olefins to construct cinnamyl aldehydes. The reaction features simple hydrocarbon substrates, metal-free conditions, and high regio- and stereoselectivity.

Selective transformation of N-(propargylic)hydroxylamines into 4-isoxazolines and acylaziridines promoted by metal salts

Cyclization of N-(propargylic)hydroxylamines catalyzed by AgBF4 afforded the corresponding 4-isoxazolines in good yields. Copper salts were found to promote the further transformation to acylaziridines. The combined use of AgBF4 and CuCl realiz