Merck
CN

767905

Sigma-Aldrich

4,4′-Dimethoxydiphenylamine

99%

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别名:
4-Biphenylamine,4,4′-dimethoxy-, 4-Methoxy-N-(4-methoxyphenyl)aniline, p,p′-Dimethoxydiphenylamine, Benzenamine,4-methoxy-N-(4-methoxypheny)-, Bis(4-methoxyphenyl)-amine, Bis(4-methoxyphenyl)amine, Bis(p-anisyl)amine, Bis(p-methoxyphenyl)amine, Di-p-anisylamine, Di-p-methoxyphenylamine, Termofleks A
经验公式(希尔记法):
C14H15NO2
CAS号:
分子量:
229.27
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.23

质量水平

检测方案

99%

形式

powder

mp

100-104 °C

SMILES string

COc1ccc(Nc2ccc(OC)cc2)cc1

InChI

1S/C14H15NO2/c1-16-13-7-3-11(4-8-13)15-12-5-9-14(17-2)10-6-12/h3-10,15H,1-2H3

InChI key

VCOONNWIINSFBA-UHFFFAOYSA-N

一般描述

4,4′-Dimethoxydiphenylamine is an aromatic amine that is used as a hole transporting material that facilitates efficiency mobility of charges in an electrochemical device.

应用

It can be used as a hole transporting material in the synthesis of 4,4′-dimethoxydiphenylamine-substituted 9,9′- bifluorenylidene with a power efficiency of ~18% which may be used in combination with an electron transporting layer in the fabrication of polymeric solar cells. It may also be used in the preparation of dimethyldiphenylamino functionalized carbazoles as electronically active materials which can potentially be used in the development of optoelectronic devices.

象形图

Exclamation markHealth hazard

警示用语:

Warning

危险分类

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Triarylene linked spacer effect for dye-sensitized solar cells
Chang, Y. J., Wu, Y. J., Chou, P. T., Watanabe, M., & Chow, T. J.
Thin Solid Films, 558, 330-336 (2014)
Diphenylamino-substituted derivatives of 9-phenylcarbazole as glass-forming hole-transporting materials for solid state dye sensitized solar cells.
Tomkeviciene A, et al.
Synthetic Metals, 162(23), 1997-2004 (2012)
Dimethyldiphenylamino-substituted carbazoles as electronically active molecular materials.
Tomkeviciene A, et al.
Dyes and Pigments, 96(2), 574-580 (2013)
Molecular-radical catalysis of the chain reaction of quinone imine with hydroquinone under the action of aromatic amines.
Varlamov VT.
Kinetics and Catalysis, 45(5), 662-675 (2004)
Thermally stable triaryl amino chromophores with high molecular hyperpolarizabilities
Spraul, Bryan K., et al.
Tetrahedron Letters, 45(16), 3253-3256 (2004)

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