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647209

Sigma-Aldrich

4-(Diphenylamino)benzaldehyde

97%

Sinônimo(s):

4-Formyltriphenylamine

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About This Item

Fórmula empírica (Notação de Hill):
C19H15NO
Número CAS:
4181-05-9
Peso molecular:
273.33
Beilstein:
2732795
Número MDL:
MFCD00145131
Código UNSPSC:
12352100
ID de substância PubChem:
24883517
NACRES:
NA.22

Ensaio

97%

forma

solid

pf

129-133 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

UESSERYYFWCTBU-UHFFFAOYSA-N

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Categorias relacionadas

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Sigma-Aldrich

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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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