123557-15-3

Upstream product

• 61066-33-9 pyrimidine-2,4,5,6(1H,3H)-tetraone 
• 445466-23-9 3-Amino-4-phenethylamino-benzoic acid methyl ester 
• 3237-50-1 5,5-dihydroxy-pyrimidine-2,4,6-trione 
• 123557-19-7 methyl 3-nitro-N⁴-phenethylaminobenzoate 
• 123557-14-2 3-nitro-N⁴-phenethylaminobenzoic acid 
• 64-04-0 phenethylamine 
• 453-71-4 3-nitro-4-fluorobenzoic acid 

Downstream Products

• 128429-09-4 t-butyl 7-methoxycarbonyl-N¹⁰-phenethylisoalloxazine-3-acetate 
• 123557-17-5 3-Carboxymethyl-2,4-dioxo-10-phenethyl-2,3,4,10-tetrahydro-benzo[g]pteridine-7-carboxylic acid 
• 123557-18-6 <7-(2-formamido-ethyl)-3-(2-acetamido-ethyl)>-3,3'-bis-phenyl-thiourea-N¹⁰-phenethylisoalloxazine 
• 128429-08-3 N³-(N-propyl)-acetamido-7-(N-propyl)-formamido-N¹⁰-phenethylisoalloxazine 
• 128429-11-8 7-methoxycarbonyl-3-(2-acetamido-ethyl)-3-phenylthiourea-N¹⁰-phenethylisoalloxazine 
• 123557-16-4 ethyl 7-methoxycarbonyl-N¹⁰-phenethylisoalloxazine-3-acetate 

Relevant academic research and scientific papers

Synthesis of bifunctionalised flavins for incorporation into well defined redox systems

The syntheses of isoalloxazines functionalised at C-7 and N-3, suitable for two point parallel face attachment to gold in the construction of flavin-gold electrodes, are described.

Construction of a Stable Flavin-Gold Electrode displaying Very Fast Electron Transfer Kinetics

The bis-phenylthiourea phenethylisoalloxazine (6) was synthesised and was attached to the gold through its thiourea side-chains; cyclic voltammetric investigation of the redox properties of the system confirmed that the flavin was a stable adsorbed species and revealed that electron transfer between the conductor and the flavin was very fast.