1313757-66-2

Upstream product

• 14235-81-5 4-Ethynylaniline 
• 105-36-2 ethyl bromoacetate 
• 1361147-63-8 N-((4-trimethylsilylethynyl)phenyl)glycine ethyl ester 
• 14108-76-0 2-(4-iodophenylamino)acetic acid ethyl ester 
• 540-37-4 p-aminoiodobenzene 

Downstream Products

• 1361147-67-2 [Fe(C₅H₄C₂C₆H₄NHCH₂CO₂C₂H₅)2] 
• 1313757-53-7 C₁₃H₁₅NO₂ 
• 1313757-57-1 C₂₃H₃₃N₃O₄ 
• 1313757-56-0 C₃₄H₄₂N₄O₆ 
• 1313757-55-9 N(α)-(4-ethynylphenyl)-N(α)-(methyl)-glycyl-valine methyl ester 
• 1313757-54-8 C₁₅H₁₄N₂O₄ 
• 1379188-93-8 C₁₁H₁₁NO₂ 
• 1313757-65-1 C₅₂H₆₄N₁₀O₈ 
• 1313757-64-0 C₄₀H₄₂N₈O₆ 
• 1313757-63-9 C₃₂H₃₈N₈O₅ 
• 1313757-62-8 C₂₉H₃₃N₇O₄ 
• 1313757-61-7 N(α)-[4-(1,1,4,4-tetracyanobuta-1,3-dien-2-yl)phenyl]-N(α)-(methyl)-glycyl-valine methyl ester 
• 1313757-60-6 C₅₂H₇₄N₈O₁₀ 
• 1313757-58-2 C₄₆H₆₄N₆O₈ 

Relevant academic research and scientific papers

Synthesis and characterization of a ferrocene-linked bis-fullerene[60] dumbbell

A new [60]fullerene dumbbell consisting of two fulleropyrrolidines connected to a central ferrocene unit by amide linkages has been prepared and fully characterized by elemental analysis, 1H NMR, UV/Vis, fluorescence and mass spectrometry. The electrochemical properties as determined by cyclic voltammetry show ground state electronic communication between the ferrocene and the fullerene units. In addition, the preparaton of a ferrocene building block for an alternative linking approach is presented. The Royal Society of Chemistry 2012.

A convenient synthesis of new chromophoric tetracyanobutadiene-scaffolded peptides via a dipolar [2+2] cycloaddition-cycloreversion reaction

Herein, we report a novel approach for the synthesis of π-conjugated peptide-based donor-acceptor (D-π-A) chromophores, by reacting electron-rich alkynes with tetracyanoethylene. The desired tetracyanobutadiene-scaffolded peptides were obtained in good yields with various optical properties, λmax: 321-492 nm, ε: 21,000-65,000 mol-1 dm3 cm-1 depending on the substitution pattern of the cyanobutadiene scaffold.