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Documenti

152765

Sigma-Aldrich

9-Anthracenecarbonitrile

97%

Sinonimo/i:

9-Cyanoanthracene

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About This Item

Formula empirica (notazione di Hill):
C15H9N
Numero CAS:
1210-12-4
Peso molecolare:
203.24
Numero CE:
214-909-7
Numero MDL:
MFCD00001242
Codice UNSPSC:
12352100
ID PubChem:
24849258
NACRES:
NA.22

Saggio

97%

Forma fisica

powder

Punto di fusione

173-177 °C (lit.)

Stringa SMILE

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
KEQZHLAEKAVZLY-UHFFFAOYSA-N

Descrizione generale

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

Applicazioni

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302 + H312 + H332

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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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
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
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
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
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
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