2770-17-4

Basic information

• Product Name: 11-phenyldibenzo[b,f][1,4]oxazepine
• Synonyms: Dibenz[b,f][1,4]oxazepine, 11-phenyl-; Dibenzo[b,f]-1,4-oxazepine, 11-phenyl-
• CAS NO: 2770-17-4
• Molecular Formula: C₁₉H₁₃NO
• Molecular Weight: 271.3126
• Mol File: 2770-17-4.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 393.2°C at 760 mmHg
• Flash Point: 155°C
• Density: 1.15g/cm³
• Vapor Pressure: 4.91E-06mmHg at 25°C
• Refractive Index: 1.635
• CAS DataBase Reference: 11-phenyldibenzo[b,f][1,4]oxazepine(CAS DataBase Reference)
• NIST Chemistry Reference: 11-phenyldibenzo[b,f][1,4]oxazepine(2770-17-4)
• EPA Substance Registry System: 11-phenyldibenzo[b,f][1,4]oxazepine(2770-17-4)

Safety Data

• Hazardous Substances Data: 2770-17-4(Hazardous Substances Data)

Upstream product

• 62469-61-8 11-chloro-dibenz<1,4>oxazepine 
• 100-58-3 phenylmagnesium bromide 
• 119-61-9 benzophenone 
• 95-55-6 2-amino-phenol 
• 104272-69-7 1-chloro-2-nitro-3-phenoxybenzene 
• 64182-61-2 1-chloro-3-fluoro-2-nitrobenzene 
• 98-88-4 benzoyl chloride 
• 342-24-5 o-fluorobenzophenone 
• 117-99-7 2-Hydroxybenzophenone 
• 583-53-9 2,3-dibromobenzene 
• 1331753-57-1 (2-(2-bromophenoxy)phenyl)(phenyl)methanone 
• 108-95-2 phenol 
• 2688-84-8 2-phenoxyaniline 
• 1493-27-2 ortho-nitrofluorobenzene 

Downstream Products

• 1316274-09-5 (-)-(S)-11-phenyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine 
• 2244-56-6 11-phenyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine 

Relevant articles and documents

Annulation of Diaryl(aryl)phosphenes and Cyclic Imines to Access Benzo-δ-phospholactams

Microwave-assisted annulation of cyclic imine dibenzo[b,f][1,4]oxazepines and diaryl(aryl)phosphenes generated from diazo(aryl)methyl(diaryl)phosphine oxides through the Wolff rearrangement accesses pentacyclic benzo-δ-phospholactams, 4b,16-dihydrodibenzo

Asymmetric Hydrogenation of Seven-Membered C=N-containing Heterocycles and Rationalization of the Enantioselectivity

Iridium(I) complexes with phosphine–phosphite ligands efficiently catalyze the enantioselective hydrogenation of diverse seven-membered C=N-containing heterocyclic compounds (eleven examples; up to 97 % ee). The P-OP ligand L3, which incorporates an ortho

Synthesis and enantioselective hydrogenation of seven-membered cyclic imines: Substituted dibenzo[b,f][1,4]oxazepines

Highly enantioselective hydrogenation of seven-membered cyclic imines, substituted dibenzo[b,f][1,4]oxazepines, was achieved, with up to 94% ee, by using the [Ir(COD)Cl]2/(S)-Xyl-C3*-TunePhos complex as the catalyst in the presence of morpholine-HCl.