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文件

647209

Sigma-Aldrich

4-二苯胺基苯甲醛

97%

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别名:
4-甲酰基三苯胺
经验公式（希尔记法）:
C19H15NO
CAS号:
4181-05-9
分子量:
273.33
Beilstein:
2732795
MDL编号:
MFCD00145131
PubChem化学物质编号:
24883517
NACRES:
NA.22

检测方案

97%

形式

solid

mp

129-133 °C (lit.)

SMILES string

O=Cc1ccc(cc1)N(c2ccccc2)c3ccccc3

InChI

1S/C19H15NO/c21-15-16-11-13-19(14-12-16)20(17-7-3-1-4-8-17)18-9-5-2-6-10-18/h1-15H

InChI key

UESSERYYFWCTBU-UHFFFAOYSA-N

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相关类别

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315 - H319 - H335

危险分类

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

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Aline M Lino et al.
Physical chemistry chemical physics : PCCP, 19(31), 20984-20990 (2017-07-27)
The styryl dye (E)-2-[3-[4-(diphenylamine) phenyl]-1-(p-tolyl)-allylidene]-malononitrile (DFTAM) was prepared by Knoevenagel condensation using homogeneous and surface bound amino catalysts. The catalysis by surface bound piperazine allowed the study of the condensation reaction at a single molecule (SM) level using total internal
Viprabha Kakekochi et al.
ChemPlusChem, 85(8), 1762-1777 (2020-08-15)
A set of four symmetric, butterfly-shaped 4-(4-(decyloxy)phenyl)-2,6-di(thiophen-2-yl)pyridine (TPY) derivatives 2TPA-TPY (TPY center and triphenylamine end groups), 2CBZ-TPY (TPY center and N-ethyl carbazole end groups), 2TPY-TPA (triphenylamine center and TPY at the periphery) and 2TPY-CBZ (N-ethyl carbazole center and TPY at
Anu Kundu et al.
Journal of fluorescence, 29(6), 1359-1369 (2019-11-16)
New series of methoxy and hydroxyl group substituted triphenylamine (TPA)-imidazole fluorescent molecules (5-(diphenylamino)-2-(1H-phenanthro[9,10-d]imidazol-2-yl)phenol (1), 5-(diphenylamino)-2-(1-phenyl-1H-phenanthro[9,10-d]imidazol-2-yl)phenol (2), 5-(diphenylamino)-2-(4,5-diphenyl-1H-imidazol-2-yl)phenol (3), 5-(diphenylamino)-2-(1,4,5-triphenyl-1H-imidazol-2-yl)phenol (4), N-(3-methoxy-4-(1H-phenanthro[9,10-d]imidazol-2-yl)phenyl)-N-phenylbenzenamine (5), N-(3-methoxy-4-(1-phenyl-1H-phenanthro[9,10-d]imidazol-2-yl)phenyl)-N-phenylbenzene amine (6), and N-(3-methoxy-4-(4,5-diphenyl-1H-imidazol-2-yl)phenyl)-N-phenylbenzenamine (7)) have been synthesized that exhibited strong solution fluorescence and molecular structure and
Danuta Sek et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 175, 24-35 (2016-12-25)
The new Schiff bases bearing anthracene unit were synthesized from 2-aminoanthracene and various aldehydes such as: benzaldehyde, 4-(diphenylamino)benzaldehyde, 9-phenanthrenecarboxaldehyde, 9-anthracenecarboxaldehyde, and biphenyl-4-carboxaldehyde, 2-naphthaldehyde. Resulted azomethines were characterized by IR, NMR (

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