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151483

Sigma-Aldrich

9-Ethyl-3-carbazolecarboxaldehyde

98%

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About This Item

Empirical Formula (Hill Notation):
C15H13NO
CAS Number:
7570-45-8
Molecular Weight:
223.27
EC Number:
231-471-2
MDL number:
MFCD00004963
UNSPSC Code:
12352100
PubChem Substance ID:
24849138
NACRES:
NA.22

Assay

98%

form

solid

mp

85-87 °C (lit.)

storage temp.

2-8°C

SMILES string

[H]C(=O)c1ccc2n(CC)c3ccccc3c2c1

InChI

1S/C15H13NO/c1-2-16-14-6-4-3-5-12(14)13-9-11(10-17)7-8-15(13)16/h3-10H,2H2,1H3

InChI key

QGJXVBICNCIWEL-UHFFFAOYSA-N

Application

9-Ethyl-3-carbazolecarboxaldehyde was used in the synthesis of poly(vinyl acetal)s (PVAcs).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Ramasamy Raj Kumar et al.
Journal of photochemistry and photobiology. B, Biology, 165, 310-327 (2016-11-14)
Formation of ruthenium(II) complexes of the type [RuH(CO)(PPh
Agata Głuszyńska et al.
Molecules (Basel, Switzerland), 24(5) (2019-03-13)
Microwave formylation of carbazole derivatives was investigated and 3-monoaldehydes were obtained in high yield. A potential DNA-binding ligand, 3-[(3-ethyl)-2-vinylbenzothiazolium]-9-N-ethyl carbazole iodide, was synthesized and characterized including spectral properties (UV-Vis absorption and fluorescence spectra). The binding selectivity and affinity of three
Poly (vinyl acetal) s containing electron-donor groups: Synthesis in homogeneous phase and their thermal properties.
Fernandez MD, et al.
Reactive functional Polymers, 68(1), 39-56 (2008)

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