184705-14-4

Upstream product

• 7677-24-9 trimethylsilyl cyanide 
• 184705-11-1 3-(hydroxymethyl)-2-ethyl-1-(phenylmethyl)-5-methoxyindole 
• 100-46-9 benzylamine 
• 184705-03-1 1-benzyl-2-ethyl-5-hydroxy-1H-indole-3-carboxylic acid methyl ester 
• 184705-08-6 3-(carbomethoxy)-2-ethyl-1-(phenylmethyl)-5-methoxyindole 
• 184705-06-4 methyl 3-(benzylamino)pent-2-enoate 
• 30414-53-0 methyl propanoyl acetate 
• 151-50-8 potassium cyanide 

Downstream Products

• 164123-34-6 3-(amidomethyl)-2-ethyl-1-(phenylmethyl)-5-hydroxyindole 
• 164083-83-4 dimethyl [3-[[3-(amidomethyl)-2-ethyl-1-(phenylmethyl)-indol-5-yl]oxy]propyl]phosphonate 
• 164083-79-8 ethyl [4-[3-(amidomethyl)-2-ethyl-1-(phenylmethyl)-indol-5-yl]oxy]butanoate 
• 1026933-81-2 C₂₈H₄₃N₂O₅PSi₂ 
• 164084-29-1 3-(amidomethyl)-2-ethyl-1-(phenylmethyl)-5-methoxyindole 

Relevant academic research and scientific papers

Synthesis of indomethacin analogues for evaluation as modulators of MRP activity

Synthesis of a range of indomethacin analogues, required for investigation in combination toxicity assays, bearing both N-benzyl and N-benzoyl groups, is described. Copyright

Isoharmine revisited: Thermal rearrangement of a 3-cyanomethyl-2- vinylindole

Thermolysis of 2-vinylindole derivative (1) led to indolylacrylonitrile (6) instead of β-carboline alkaloid isoharmine (4). Latter was prepared by following the conventional method and was fully characterized.