28161-60-6

Basic information

• Product Name: trans-1-Amino-2,3-diphenylaziridine
• Synonyms: trans-1-Amino-2,3-diphenylaziridine
• CAS NO: 28161-60-6
• Molecular Formula: C₁₄H₁₄N₂
• Molecular Weight: 210.27436
• Mol File: 28161-60-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: trans-1-Amino-2,3-diphenylaziridine(CAS DataBase Reference)
• NIST Chemistry Reference: trans-1-Amino-2,3-diphenylaziridine(28161-60-6)
• EPA Substance Registry System: trans-1-Amino-2,3-diphenylaziridine(28161-60-6)

Safety Data

• Hazardous Substances Data: 28161-60-6(Hazardous Substances Data)

Upstream product

• 29392-97-0 2-[(2RS,3RS)-2,3-diphenylaziridin-1-yl]isoindoline-1,3-dione 
• 103-30-0 (E)-1,2-diphenyl-ethene 

Downstream Products

• 60211-79-2 (2r,3t-diphenyl-aziridin-1-yl)-(5-phenyl-3-p-tolyl-isoxazol-4-ylmethylene)-amine 
• 134225-41-5 N-((phenylethynyl)methylene)-trans-2,3-diphenyl-1-aziridinamine 
• 134340-43-5 (1,4-Dioxa-spiro[4.5]dec-8-ylidene)-((2S,3S)-2,3-diphenyl-aziridin-1-yl)-amine 
• 134340-45-7 ((2S,3S)-2,3-Diphenyl-aziridin-1-yl)-non-(E)-ylidene-amine 
• 134340-44-6 (1-Benzyl-piperidin-4-ylidene)-((2S,3S)-2,3-diphenyl-aziridin-1-yl)-amine 
• 74346-38-6 6-(trans-2,3-Diphenylaziridin-1-yl-imino)-1-hexene 
• 134340-42-4 ((2S,3S)-2,3-Diphenyl-aziridin-1-yl)-[1-methyl-3-phenyl-prop-(E)-ylidene]-amine 
• 78926-45-1 o-(trans-2,3-diphenylaziridin-1-yliminomethyl)styrene 
• 134078-19-6 C₂₃H₂₀N₂ 
• 124021-74-5 1-[2-(6-{[(Z)-(2S,3S)-2,3-Diphenyl-aziridin-1-ylimino]-methyl}-benzo[1,3]dioxol-5-yl)-ethyl]-5-thioxo-pyrrolidin-2-one 
• 74365-62-1 trans-N-<<2-<(Z)-2-Butenyl>phenyl>methylene>-2,3-diphenyl-1-aziridinamine 
• 74346-43-3 trans-N-<<2-<(E)-2-Butenyl>phenyl>methylene>-2,3-diphenyl-1-aziridinamine 
• 134078-21-0 [1-Cuban-1-yl-meth-(Z)-ylidene]-((2R,3R)-2,3-diphenyl-aziridin-1-yl)-amine 
• 136178-44-4 ((2S,3S)-2,3-Diphenyl-aziridin-1-yl)-[1-(1-prop-2-ynyl-1H-indol-2-yl)-meth-(E)-ylidene]-amine 

Relevant articles and documents

Lithium Aluminum Hydride Reduction of N-Aziridinylimines to Hydrocarbons

The hydride reduction of ketone and aldehyde N-aziridinylimines is reported.Unlike most other hydrazone reductions, the reaction proceeds at room temperature under non-acidic conditions, providing an unusually mild carbonyl-to-methylene conversion.