214663
2-Ethylanthracene
98%
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About This Item
Empirical Formula (Hill Notation):
C16H14
CAS Number:
Molecular Weight:
206.28
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
257-788-6
MDL number:
Assay:
98%
Form:
solid
InChI key
ZXAGXLDEMUNQSH-UHFFFAOYSA-N
InChI
1S/C16H14/c1-2-12-7-8-15-10-13-5-3-4-6-14(13)11-16(15)9-12/h3-11H,2H2,1H3
SMILES string
CCc1ccc2cc3ccccc3cc2c1
assay
98%
form
solid
mp
152-153 °C (lit.)
General description
Photophysics and photochemistry of 2-ethylanthracene (2EA) adsorbed on silica has been studied at a silica/air interface.
Application
2-Ethylanthracene was used as photosensitizer during the photodissociation of p-nitrobenzyl esters of alkylsulphonic acids. It was used in the synthesis of thioxanthone-2-ethyl anthracene.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Thioxanthone-ethyl anthracene.
Balta D-K and Arsu N.
Journal of Photochemistry and Photobiology A: Chemistry, 257, 54-59 (2013)
Peter A Beckmann et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 19(18), 2423-2436 (2018-06-30)
We report solid-state nuclear magnetic resonance 1 H spin-lattice relaxation, single-crystal X-ray diffraction, powder X-ray diffraction, field emission scanning electron microscopy, and differential scanning calorimetry in solid samples of 2-ethylanthracene (EA) and 2-ethylanthraquinone (EAQ) that have been physically purified in
Photochemical dissociation of p-nitrobenzyl 9, 10-dimethoxyanthracene-2-sulphonate via intramolecular electron transfer.
Yamaoka T, et al.
J. Chem. Soc. Perkin Trans. II, 10, 1709-1714 (1990)
Photophysical and photochemical processes of 2-methyl, 2-ethyl, and 2-tert-butylanthracenes on silica gel. A substituent effect study.
Dabestani R, et al.
The Journal of Physical Chemistry B, 104(44), 10235-10241 (2000)
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