10125-39-0

Basic information

• Product Name: 1-Triazene, 3,3-diethyl-1-(4-nitrophenyl)-
• CAS NO: 10125-39-0
• Molecular Formula: C10H14N4O2
• Molecular Weight: 222.247
• Mol File: 10125-39-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-Triazene, 3,3-diethyl-1-(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Triazene, 3,3-diethyl-1-(4-nitrophenyl)-(10125-39-0)
• EPA Substance Registry System: 1-Triazene, 3,3-diethyl-1-(4-nitrophenyl)-(10125-39-0)

Safety Data

• Hazardous Substances Data: 10125-39-0(Hazardous Substances Data)

Upstream product

• 100-01-6 4-nitro-aniline 
• 109-89-7 diethylamine 

Downstream Products

• 171364-83-3 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzene 
• 64308-51-6 N-morpholino-4-nitrobenzenesulfonamide 
• 98-95-3 nitrobenzene 
• 586-78-7 para-nitrophenyl bromide 
• 13122-36-6 nitrobenzene-4-d 
• 100-02-7 4-nitro-phenol 
• 636-98-6 p-nitrobenzene iodide 
• 350-46-9 4-Fluoronitrobenzene 

Relevant articles and documents

Catalytic conversion of aryl triazenes into aryl sulfonamides using sulfur dioxide as the sulfonyl source

Various sulfonamides have been synthesized from triazenes and sulfur dioxide. In the presence of just a catalytic amount of BF3· OEt2, a series of 1-aryl-triazenes were converted into sulfonyl hydrazines in good to excellent yields. When using CuCl2 as the catalyst, the corresponding sulfonamides can be produced from the 1-aryl triazenes in good yields. This journal is the Partner Organisations 2014.

Synthesis of 1-aryl-3,3-disubstituted triazenes on ion-exchange resin support

Diazonium ions have been immobilized on a cation exchanger followed by N-coupling on a 2-amine to give the 3,3-disubstituted-1-aryltriazenes as the only product. Reaction is clean and work up procedure simple.