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Key Documents

805416

Sigma-Aldrich

5H-Pyrido[3,2-b]indole

Synonym(s):

δ-Carboline

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About This Item

Empirical Formula (Hill Notation):
C11H8N2
CAS Number:
Molecular Weight:
168.19
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

99% (HPLC)

Quality Level

form

powder

mp

209-214 °C

SMILES string

C1(C=CC=C2)=C2C(N=CC=C3)=C3N1

InChI

1S/C11H8N2/c1-2-5-9-8(4-1)11-10(13-9)6-3-7-12-11/h1-7,13H

InChI key

NSBVOLBUJPCPFH-UHFFFAOYSA-N

Application

Novel aromatic amine compound for organic electroluminescent device, illuminating device and display.

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Spectral and photophysical properties of the δ-carboline anhydrobase (N1-methyl-5H-pyrido[3,2-b]indole).
Balon M, et al.
Chemical Physics, 302(1-3), 13-20 (2004)
Manipulation of electron deficiency of δ-carboline derivatives as bipolar hosts for blue phosphorescent organic light-emitting diodes with high efficiency at 1000 cd m-2.
Zhang Z, et al.
Journal of Material Chemistry C, 4, 4226-4235 (2016)
Manipulation of electron deficiency of δ-carboline derivatives as bipolar hosts for blue phosphorescent organic light-emitting diodes with high efficiency at 1000 cd m-2.
Zhang Z,et al.
Journal of Material Chemistry C, 4(19), 4226-4235 null
Thermally activated delayed fluorescence of co-deposited copper(i) complexes: cost-effective emitters for highly efficient organic light-emitting diodes.
Wang Z, et al.
Journal of Material Chemistry C, 5, 6982-6988 (2017)
Controlling the exciton lifetime of blue thermally activated delayed fluorescence emitters using a heteroatom-containing pyridoindole donor moiety.
Kim G H, et al.
Materials Horizons, 4, 619-624 (2017)

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