34361-08-5

Upstream product

• 3155-22-4 N-(4-nitrobenzylidene)-N'-(4-nitrophenyl)hydrazine 
• 100-16-3 4-nitrophenylhydrazone 
• 555-16-8 4-nitrobenzaldehdye 
• 26346-63-4 p-nitrobenzaldehyde p-nitrophenylhydrazone 

Downstream Products

• 40166-02-7 4-[(4-nitro-phenyl)-(4-nitro-phenylhydrazono)-methyl]-morpholine 
• 79864-61-2 C₂₃H₁₆N₄O₅ 
• 839684-37-6 1-(p-nitrophenyl)-3-(p-nitrophenyl)pyrazolo[4',5':1,2]fullerene[60] 
• 128694-02-0 1,3-Bis-(4-nitro-phenyl)-5-(1,1,2-trimethyl-allyl)-1H-[1,2,4]triazole 
• 128694-09-7 5-Ethylsulfanyl-6,6,7,7-tetramethyl-2,4-bis-(4-nitro-phenyl)-1,3,4-triaza-bicyclo[3.2.0]hept-2-ene 
• 79864-60-1 C₂₃H₁₆N₄O₅ 
• 128694-06-4 5-Ethoxy-6,6,7,7-tetramethyl-2,4-bis-(4-nitro-phenyl)-1,3,4-triaza-bicyclo[3.2.0]hept-2-ene 

Relevant academic research and scientific papers

Nitration of fullerene derivatives under mild conditions

A new family of N-(2,4-dinitrophenyl)-2-pyrazolino[60]fullerene derivatives has been synthesized by electrophilic nitration using nitronium triflate. As evidenced by CV and OSWV experiments, these species show enhanced electron-accepting properties (up to

1,3-Dipolar Cycloadditions of 2-Ethoxy- and 2-(Ethylthio)-1-azetines with Nitrile Oxides, Nitrile Ylides and Nitrilimines: An Unexpected 1,2,4-Triazole Formation.

2-Ethoxy- and 2-(ethylthio)-1-azetines readily undergo 1,3-dipolar cycloadditions with nitrile oxides and nitrile ylides to give stable 4,5-bicyclic cycloadducts.With nitrilimines, however, the expected 1,3-dipolar cycloadducts and/or unexpected ring-open