155064-31-6

Basic information

• Product Name: 1-Triazene, 3,3-diethyl-1-(4-ethynylphenyl)-
• CAS NO: 155064-31-6
• Molecular Formula: C12H15N3
• Molecular Weight: 201.271
• Mol File: 155064-31-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Triazene, 3,3-diethyl-1-(4-ethynylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Triazene, 3,3-diethyl-1-(4-ethynylphenyl)-(155064-31-6)
• EPA Substance Registry System: 1-Triazene, 3,3-diethyl-1-(4-ethynylphenyl)-(155064-31-6)

Safety Data

• Hazardous Substances Data: 155064-31-6(Hazardous Substances Data)

Upstream product

• 630104-26-6 3,3-diethyl-1-(4-iodophenyl)triaz-1-ene 
• 540-37-4 p-aminoiodobenzene 
• 134856-57-8 1-[4-[2-(trimethylsilyl)ethynyl]phenyl]-3,3-diethyltriazene 

Downstream Products

• 230958-48-2 1,3,5-tris-((4-iodophenyl) ethynyl) benzene 
• 156264-85-6 C₂₇H₃₅N₃Si 
• 210905-41-2 3,3-diethyl-1-[4-({4-[(trimethylsilyl)ethynyl]phenyl}ethynyl)phenyl]-1-triazene 
• 762262-27-1 C₂₆H₂₂BrN₃ 
• 1187449-16-6 C₇₃H₁₇N₃ 
• 1327277-71-3 C₂₆H₂₂IN₃ 
• 1327277-70-2 C₂₀H₁₉N₃ 
• 1327277-69-9 1-(4-(2-(4-bromophenyl)ethynyl)phenyl)-3,3-diethyltriazene 
• 155064-34-9 C₇₅H₇₄N₁₂Si 

Relevant articles and documents

Symmetrically backfolded molecules emulating the self-similar features of a Sierpinski triangle

We synthesized self-similar molecules (G3 and G2; based on phenylalkynyl backbones) with symmetrically backfolded shapes inspired by the famous fractal of a Sierpinski triangle. Unlike the more traditional, starburst dendrimers, the centripetal-shaped Sierpinski molecules feature side branches symmetrically bent away from the growth direction of the main branch, thus contrasting the natural-tree shape. Molecule G3 exhibits three distinct levels of the structural hierarchy comprising the primary, secondary and tertiary branches, while the smaller G2 contains only features of the 1st and 2nd orders. In spite of the much larger conjugated backbone of G3, its solution UV-vis absorption and fluorescence exhibit no red shift relative to G2. In a test of nitrobenzene sensing, a thin film of G3 deposited from THF was more sensitively quenched in fluorescence than the smaller G2.

Rapid solution and solid phase synthesis of monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5-thiopheneethynylene)]s

Monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5-thiopheneethynylene)] s, new candidates for molecular wires, were rapidly synthesized via an iterative divergent/convergent doubling strategy in solution as well as on Merrifield's resin.

A novel in situ deprotection/coupling and iterative divergent/convergent strategy for the synthesis of oligo(1,4-phenyleneethynylene)s

A novel in situ deprotection/coupling and iterative divergent/convergent strategy for the synthesis of oligo(1,4-phenyleneethynylene)s is described.