70093-24-2

Basic information

• Product Name: 1-[2-(4-fluoro-phenyl)-indol-3-yl]-ethanone
• CAS NO: 70093-24-2
• Molecular Weight: 253.276
• Mol File: 70093-24-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-[2-(4-fluoro-phenyl)-indol-3-yl]-ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2-(4-fluoro-phenyl)-indol-3-yl]-ethanone(70093-24-2)
• EPA Substance Registry System: 1-[2-(4-fluoro-phenyl)-indol-3-yl]-ethanone(70093-24-2)

Safety Data

• Hazardous Substances Data: 70093-24-2(Hazardous Substances Data)

Upstream product

• 403-42-9 1-(4-fluorophenyl)ethanone 
• 100-63-0 phenylhydrazine 
• 127-19-5 N,N-dimethyl acetamide 
• 782-17-2 2-(4-fluorophenyl)indole 
• 1994-40-7 1-(1-(4-fluorophenyl)ethylidene)-2-phenylhydrazine 
• 108-24-7 acetic anhydride 

Downstream Products

• 70093-25-3 1-[2-(4-fluoro-phenyl)-indol-3-yl]-3-morpholin-4-yl-propan-1-one 

Relevant articles and documents

Iminyl-radicals by electrochemical decarboxylation of α-imino-oxy acids: construction of indole-fused polycyclics

Iminyl radicals are reactive intermediates that can be used for the construction of various valuable heterocycles. Herein, the electrochemical decarboxylation of α-imino-oxy acids for the generation of iminyl radicals has been accomplished under exogenous-oxidant- and metal-free conditions through the use ofnBu4NBr as a mediator. The resulting iminyl radicals undergo intramolecular cyclization smoothly with the adjacent (hetero)arenes to afford a series of indole-fused polycyclic compounds.