1354381-85-3

Upstream product

• 446-52-6 2-Fluorobenzaldehyde 
• 100-01-6 4-nitro-aniline 
• 536-74-3 phenylacetylene 
• 1354381-95-5 N-(4-nitrophenyl)-3-amino-3-(3,4-difluorophenyl)-1-phenylprop-1-yne 
• 1354381-94-4 N-(4-nitrophenyl)-3-amino-3-(2,5-difluorophenyl)-1-phenylprop-1-yne 

Downstream Products

• 1354381-95-5 N-(4-nitrophenyl)-3-amino-3-(3,4-difluorophenyl)-1-phenylprop-1-yne 
• 1093164-70-5 2-(2-fluorophenyl)-6-nitro-4-phenylquinoline 
• 1354382-16-3 2-(3-fluorophenyl)-6-nitro-4-phenylquinoline 
• 1171310-24-9 2-(4-fluorophenyl)-6-nitro-4-phenylquinoline 
• 1354382-20-9 C₂₁H₁₂F₂N₂O₂ 
• 1354382-22-1 2-(2,4-difluorophenyl)-6-nitro-4-phenylquinoline 
• 1354382-24-3 2-(2,5-difluorophenyl)-6-nitro-4-phenylquinoline 
• 1354382-26-5 C₂₁H₁₂F₂N₂O₂ 
• 2378-28-1 3-(2-fluorophenyl)-1-phenyl-2-propen-1-one 
• 100-01-6 4-nitro-aniline 

Relevant academic research and scientific papers

Microwave promoted one-pot preparation of fluorinated propargylamines and their chemical transformation

A series of fluorinated propargylamines have been synthesized from the one-pot three-component reaction of fluorobenzaldehyde, aniline and phenylacetylene under solvent-free and microwave irradiation. The fluorinated propargylamines were then further transformed to chalcones or quinoline derivatives respectively depending on the different structures of propargylamines.