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Key Documents

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152765

Sigma-Aldrich

9-Anthracenecarbonitrile

97%

Sinónimos:

9-Cyanoanthracene

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About This Item

Fórmula empírica (notación de Hill):
C15H9N
Número de CAS:
1210-12-4
Peso molecular:
203.24
EC Number:
214-909-7
MDL number:
MFCD00001242
UNSPSC Code:
12352100
PubChem Substance ID:
24849258
NACRES:
NA.22

assay

97%

form

powder

mp

173-177 °C (lit.)

SMILES string

N#Cc1c2ccccc2cc3ccccc13

InChI

1S/C15H9N/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9H

InChI key

KEQZHLAEKAVZLY-UHFFFAOYSA-N

General description

The fluorescence excitation spectra of 9-anthracenecarbonitrile has been studied.

Application

9-Anthracenecarbonitrile was used to study the mechanism of charge separation within phenothiazine (PTZH) or phenoxazine (PXZH), and 9-cyanoanthracene(electron acceptor).

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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K Szarka et al.
Biochemistry, 40(49), 14806-14811 (2001-12-26)
It has been shown that one of the 12 serine residues within the 23 kDa segment of myosin subfragment 1 can be covalently modified with a fluorescent probe 9-anthroylnitrile (ANN) [Hiratsuka, T. (1989) J. Biol. Chem. 264 (30), 18188-18194]. To
Reika Kanya et al.
The Journal of chemical physics, 121(19), 9489-9497 (2004-11-13)
Fluorescence excitation spectra of the S(1)-S(0) origin band of 9-cyanoanthracene have been observed under a uniform electric field up to 200 kV/cm to explore pendular-state spectrum of an asymmetric-top molecule close to the strong field limit. The observed spectra exhibit
O A Andreev et al.
Journal of muscle research and cell motility, 16(4), 353-367 (1995-08-01)
A serine residue located in the active site of myosin head (S1) was labelled by 9-anthroylnitrile, an amino group located in the central domain of S1 was labelled by 7-diethylamino-3-(4'-isothio-cyanato-phenyl)-4-methylcoumari n, a cysteine residue located near the C-terminus of S1
Franciszek K Główka et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 839(1-2), 54-61 (2006-03-23)
A new indirect RP-HPLC method was developed for determination of small, ng/ml, concentrations of triamcinolone (TMC) in human plasma, in presence of endogenous corticosteroids: cortisol (hydrocortisone, F), cortisone (E) and their metabolites, after administration of TMC in a free alcohol
N Shibata et al.
Journal of chromatography. B, Biomedical sciences and applications, 706(2), 191-199 (1998-04-29)
A new method for simultaneous determination of glucocorticoids (GCs) in plasma or urine by high-performance liquid chromatography (HPLC) with fluorimetric detection has been developed. Following extraction with ethyl acetate using a reversed-phase disposable cartridge, the six GCs [cortisol (F), cortisone
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