263891-70-9

Upstream product

• 41019-17-4 5-chloro-2-phenylindole-3-carboxaldehyde 
• 122-00-9 para-methylacetophenone 

Downstream Products

• 1246385-59-0 5-((E)-3-(5-chloro-2-phenyl-1H-indol-3-yl)-1-p-tolylallylidene)pyrimidine-2,4,6(1H,3H,5H)trione 
• 1333387-21-5 C₃₁H₂₄ClN₃O₃ 
• 1333387-40-8 C₃₆H₂₃ClN₄O₃ 
• 1333387-12-4 C₂₇H₁₈ClN₃O 
• 1277186-88-5 C₃₁H₂₄ClN₃ 
• 1428141-73-4 C₂₇H₂₀ClN₃O 
• 1428142-18-0 C₂₈H₂₀ClN₃O₂ 
• 1428142-09-9 C₂₇H₂₁ClN₄O 
• 1428142-00-0 C₂₈H₂₁ClN₄OS 
• 1428141-91-6 C₂₈H₂₁ClN₄O₂ 
• 1428141-82-5 C₃₃H₂₂ClN₅O₃ 

Relevant academic research and scientific papers

Synthesis and biological activities of some 5-substituted 2-phenyl-3-(6-aryl-3-cyano-2-substituted pyridin-4-yl) indoles

3-(5′-Substituted-2′-phenyl-1 H-indol-3′-yl)-1 -phenylprop-2-en-1 -ones (2) were prepared from indole-3-carboxyaldehydes (1) and 4-substitutedacetophenones in presence of piperidine. Compounds (2) were subjected to cyclocondensation with ethyl cyanoacetat

Synthesis, antioxidant and DNA cleavage activities of novel indole derivatives

A new series of novel indole derivatives containing barbitone moiety (5a-i) are synthesized by simple and efficient condensation of chalcones (3a-i) with barbituric acid (4). The synthesized compounds are screened for their antioxidant (free radical scave

Synthesis of new indolyl benzodiazepines and thier DNA cleavage and antimicrobial activities

2,5-Disubstituted indole aldehydes (1b) were reacted with substituted acetophenones (2a-e) in presence of base to yield the respective chalcones (3a-e). Chalcones were then reacted with substituted orthophenylenediamines to obtain title compounds (4a-e).