188844-98-6

Basic information

• Product Name: Benzenamine, N-[4-(1,1-dimethylethyl)phenyl]-2-nitro-
• CAS NO: 188844-98-6
• Molecular Formula: C16H18N2O2
• Molecular Weight: 270.331
• Mol File: 188844-98-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-[4-(1,1-dimethylethyl)phenyl]-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-[4-(1,1-dimethylethyl)phenyl]-2-nitro-(188844-98-6)
• EPA Substance Registry System: Benzenamine, N-[4-(1,1-dimethylethyl)phenyl]-2-nitro-(188844-98-6)

Safety Data

• Hazardous Substances Data: 188844-98-6(Hazardous Substances Data)

Upstream product

• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 88-74-4 2-nitro-aniline 
• 769-92-6 4-tert-Butylaniline 
• 1493-27-2 ortho-nitrofluorobenzene 

Downstream Products

• 512178-34-6 N-(4-tert-butylphenyl)benzene-1,2-diamine 
• 188845-06-9 N-{2-[(4-tert-Butyl-phenyl)-methyl-amino]-phenyl}-terephthalamic acid methyl ester 
• 188845-09-2 4-(2-tert-Butyl-5-methyl-5H-dibenzo[b,e][1,4]diazepin-11-yl)-benzoic acid methyl ester 
• 188845-03-6 N-(4-tert-Butyl-phenyl)-N-methyl-benzene-1,2-diamine 
• 1221892-58-5 C₂₃H₂₃N₃O 

Relevant articles and documents

Palladium(0)-catalyzed amination, stille coupling, and Suzuki coupling of electron-deficient aryl fluorides

The amination of 2-fluoronitrobenzene was Pd(0) catalyzed at 65 °C in DMF, and the effectiveness of the catalysis was ligand-dependent. Among the five catalyst systems investigated, Pd(PPh3)4 was the most effective catalyst. The cont

A new series of N-substituted tetraphenylethene-based benzimidazoles: Aggregation-induced emission, fast-reversible mechanochromism and blue electroluminescence

Four new N-substituted tetraphenylethene-based benzimidazoles N-R-2-(4-(1,2,2-triphenylvinyl)phenyl)-1H-benzo[d]imidazoles (R = phenyl (3a), R = 4-(tert-butyl)phenyl (3b), R = n-butyl (3c), R = n-hexyl (3d)) were synthesized conveniently by cyclization reaction of 4-tetraphenylenthenealdehyde with N-substituted ortho-nitroaniline. The four compounds exhibit typical aggregation-induced emission (AIE) property with relatively high solid state absolute fluorescence quantum yields (38.1–65.7%) and fast-recoverable mechanochromism property with solid-state fluorescence change between blue and yellow-green. They are thermally stable with decomposition temperatures above 319 °C. Both of multilayer electroluminescence devices fabricated with compounds 3b and 3c as emitters are blue emission. The turn-on voltage of device based on compound 3b is 3.3 V with maximum luminance and current efficiency of 2470 cd/m2 and 1.48 cd/A, respectively.

Novel bemzimidazole-carbazole derivative, preparation method thereof and organic light-emitting diode using the same

The present invention refers to of organic light-emitting device having phosphorescent blue emitting materials and can be used for high-benzimidazol-carbazole derivatives and their manufacturing method relates to, novel benzimidazole-carbazole derivatives the present invention according to an electronic it is a donator cover and antiviral electronic it is a receptor benzimidazole the combustion furnace through a blue of phosphors-emitting diodes for emitting sufficient energy to corresponding to blue has exhibits a good therefor, thermal stability and conformational invention have superior stability to in producing a thin film for an organic light-emitting device, of the physical properties of the device even at high temperatures and display good as a material of a luminescent layer without changing them since performance is kept at a, using the same useful as emitting materials for an organic light-emitting device can be used. (by machine translation)