1610621-75-4

Basic information

• Product Name: 2-(perfluorophenyl)-4-phenyl-2,3-dihydro-1H-benzo-1,5-diazepine
• Synonyms: 2-(perfluorophenyl)-4-phenyl-2,3-dihydro-1H-benzo-1,5-diazepine
• CAS NO: 1610621-75-4
• Molecular Weight: 388.34
• Mol File: 1610621-75-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(perfluorophenyl)-4-phenyl-2,3-dihydro-1H-benzo-1,5-diazepine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(perfluorophenyl)-4-phenyl-2,3-dihydro-1H-benzo-1,5-diazepine(1610621-75-4)
• EPA Substance Registry System: 2-(perfluorophenyl)-4-phenyl-2,3-dihydro-1H-benzo-1,5-diazepine(1610621-75-4)

Safety Data

• Hazardous Substances Data: 1610621-75-4(Hazardous Substances Data)

Upstream product

• 54081-32-2 3-(pentafluorophenyl)-1-phenylprop-2-en-1-one 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 1610621-78-7 1,2,3,4-tetrafluoro-6a-phenyl-6a,7-dihydrobenzimidazo[1,2-a]quinoline 

Relevant articles and documents

Reactions of polyfluorochalcones with o- and p-phenylenediamines. Synthesis and intramolecular transformations of polyfluorinated 2,4-diaryl-2,3-dihydrobenzo-1H-1,5-diazepines

Polyfluorochalcones react with o-phenylenediamine in ethanol and 2-propanol in the presence of triethylamine or benzyltriethylammonium chloride (TEBAC) affording polyfluorinated 2,4-diaryl-2,3-dihydrobenzo-1H-1,5-diazepines. Along with the latter in the presence of triethylamine Michael aza-adducts presumably formed, and at the use of TEBAC in 2-propanol products of intramolecular cyclization and rearrangement of benzo-1,5-diazepines, dihydrobenzimidazo[1,2-a]quinolines were obtained. The reactions of polyfluorochalcones with p-phenylenediamine in ethanol or DMF proceed mostly with the substitution of the para-fluorine atom in the perfluorophenyl rings.