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25 G
€141.00
About This Item
Empirical Formula (Hill Notation):
C15H13NO
CAS Number:
Molecular Weight:
223.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
mp
85-87 °C (lit.)
functional group
aldehyde
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)[1].
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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Agata Głuszyńska et al.
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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
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Journal of photochemistry and photobiology. B, Biology, 165, 310-327 (2016-11-14)
Formation of ruthenium(II) complexes of the type [RuH(CO)(PPh
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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