2715-01-7

Basic information

• Product Name: 2-nitro-N-phenyl-4-(trifluoromethyl)aniline
• CAS NO: 2715-01-7
• Molecular Formula: C₁₃H₉F₃N₂O₂
• Molecular Weight: 282.218
• Mol File: 2715-01-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 338.3°C at 760 mmHg
• Flash Point: 158.4°C
• Density: 1.405g/cm³
• Vapor Pressure: 9.9E-05mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: 2-nitro-N-phenyl-4-(trifluoromethyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-nitro-N-phenyl-4-(trifluoromethyl)aniline(2715-01-7)
• EPA Substance Registry System: 2-nitro-N-phenyl-4-(trifluoromethyl)aniline(2715-01-7)

Safety Data

• Hazardous Substances Data: 2715-01-7(Hazardous Substances Data)

Upstream product

• 121-17-5 2-chloro-3-nitro-5-trifluoromethylbenzene 
• 62-53-3 aniline 
• 108-86-1 bromobenzene 
• 400-98-6 4-trifluoromethyl-2-nitroaniline 
• 367-86-2 1-fluoro-2-nitro-4-trifluoromethyl-benzene 

Downstream Products

• 1427-14-1 2-methyl-1-phenyl-5-(trifluoromethyl)-1H-benzo[d]imidazole 
• 1651-43-0 2-amino-N-phenyl-4-(trifluoromethyl)aniline 

Relevant articles and documents

Ni-Catalyzed Dual C-H Annulation of Benzimidazoles with Alkynes for Synthesis of π-Extended Heteroarenes

Transition metal catalyzed dual C-H activation and annulation with alkynes was an attractive protocol to construct polycyclic π-extended structures. However, most of them were dominated by noble metal catalysts. Disclosed herein was the study of base-metal Ni-catalysis for dual C-H annulation of N-aromatic imidazole, which produced a range of desired polycyclic aza-quinolines in 48-95% yields. The use of bifunctional phosphine oxide ligand proved to be critical for success.

Simple NIR complexes and their applicability in dye-sensitized solar cells

Novel nickel(II)benzo-diimino-semiquinonate and palladium(II)benzo-imino- semiquinonate complexes were synthesized, tested regarding their applicability in dye sensitized solar cells, and characterized optically and electrochemically. All the dyes showed a strong absorption in the near infrared region. Various electron-withdrawing substituents were introduced into the complex ligands and evaluated with respect to the effect on the energy level of the frontier molecular orbitals. Energetically suitable complexes were then tested in TiO2 based dye-sensitized solar cells with different iodide-based electrolytes. Two of them exhibited energy conversion abilities suggesting their candidacy as co-sensitizers to known visible light-absorbing dyes in order to extend the spectral window used for light harvesting into the infrared region to increase the total conversion efficiency of the cell.

Benzodiazepines with psychotropic activity. 3. N-aryl- and N-heteroaryl-1H-1,5-benzodiazepine-2,4-(3H,5H)-diones

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