4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline
Current location:Home > Our Products > 4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline
4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline
- Name4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline
- CAS29312-59-2
- Purity99%
Product Details
Top Quality 4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline 29312-59-2 Hot Sell In Stock
- Molecular Formula:C25H22 N2
- Molecular Weight:350.463
- Vapor Pressure:2.19E-10mmHg at 25°C
- Boiling Point:506.6°Cat760mmHg
- Flash Point:260.2°C
- PSA:16.13000
- Density:1.107g/cm3
- LogP:6.14860
4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline(Cas 29312-59-2) Usage
|
Chemical compound |
4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline |
|
Common uses |
materials science and organic chemistry |
|
Versatile compound |
applications in organic electronic materials such as OLEDs and organic photovoltaic cells |
|
General Description |
4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline is a chemical compound that is commonly used in materials science and organic chemistry. It is a highly versatile compound, with applications in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells. 4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline exhibits good thermal stability and solubility in common organic solvents, making it a valuable building block for the design and synthesis of new organic materials. Additionally, its unique molecular structure and electron-rich properties make it a promising candidate for the development of functional organic molecules with potential applications in various fields, including optoelectronics and organic semiconductor devices. Overall, 4-(2,6-diphenyl-4-pyridyl)-N,N-dimethylaniline is a valuable compound with diverse applications in materials science and organic chemistry. |
InChI:InChI=1/C25H22N2/c1-27(2)23-15-13-19(14-16-23)22-17-24(20-9-5-3-6-10-20)26-25(18-22)21-11-7-4-8-12-21/h3-18H,1-2H3
29312-59-2 Relevant articles
Acid-catalyzed tandem reaction for the synthesis of pyridine derivatives via C=C/C(sp3)-N bond cleavage of enones and primary amines
Mao, Zhong-Yuan,Liao, Xiao-Yun,Wang, Heng-Shan,Wang, Chun-Gu,Huang, Ke-Bin,Pan, Ying-Ming
, p. 13123 - 13129 (2017/03/11)
A one-pot acid-catalyzed tandem reaction...
Silver(I) Complexes of Diphenylpyridines: Crystal Structures, Luminescence Studies, Theoretical Insights, and Biological Activities
Wang, De-Hui,Zhang, Yuan,Wang, Yu-Tong,Feng, Hui-Yan,Chen, Yong,Zhao, De-Zhi
, p. 323 - 332 (2017/03/09)
A series of simple two-coordinated catio...
Ultrasound-Mediated Synthesis of 2,4,6-Triaryl-Pyridines Using MgAl2O4 Nanostructures
Zarnegar,Safari,Borjian-Borujeni
, p. 1683 - 1691 (2015/02/05)
Nanocrystalline MgAl2O4 was found to be ...
Nano-Fe3O4-supported, hydrogensulfate ionic liquid-catalyzed, one-pot synthesis of polysubstituted pyridines
Alinezhad, Heshmatollah,Tajbakhsh, Mahmood,Ghobadi, Neda
supporting information, p. 1964 - 1976 (2015/08/18)
Anchoring 1-methyl-3-(triethoxysilylprop...
29312-59-2 Process route
-
-
136879-59-9
N-(diphenylphosphinyl)-3-
-1-phenyl-2-propenimine
-
-
29312-59-2
4-(2,6-diphenylpyridin-4-yl)-N,N-dimethylaniline
-
-
100-10-7
4-dimethylamino-benzaldehyde
| Conditions | Yield |
|---|---|
|
With
toluene-4-sulfonic acid;
In
xylene;
for 48h;
Heating;
|
16% 27% |
-
-
106351-59-1
C32H27N3O
-
-
29312-59-2
4-(2,6-diphenylpyridin-4-yl)-N,N-dimethylaniline
-
-
103-71-9
phenyl isocyanate
| Conditions | Yield |
|---|---|
|
Thermodynamic data;
EA = 96 kJ/mol, ΔH(excit.) = 93 kJ/mol, ΔS(excit.) = -77 J/molK;;
|
29312-59-2 Upstream products
-
32728-09-9
4-(4-dimethylamino-phenyl)-2,6-diphenyl-pyrylium; chloride
-
631-61-8
ammonium acetate
-
98-86-2
acetophenone
-
100-10-7
4-dimethylamino-benzaldehyde
Related products
-
2-[2-(4-methylcyclohex-3-en-1-yl)propyl]tetrahydrofuran
CAS:94278-45-2
-
4-Methyl-5-nitroimidazole
CAS:14003-66-8
-
(2,6-dichlorophenyl) (4-hydroxyphenyl) ketone
CAS:61002-53-7