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MilliporeSigma

152765

9-Anthracenecarbonitrile

97%

Synonym(s):

9-Cyanoanthracene

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About This Item

Empirical Formula (Hill Notation):
C15H9N
CAS Number:
1210-12-4
Molecular Weight:
203.24
NACRES:
NA.22
PubChem Substance ID:
24849258
UNSPSC Code:
12352100
EC Number:
214-909-7
MDL number:
MFCD00001242
Assay:
97%
Form:
powder

Key Documents

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InChI key

KEQZHLAEKAVZLY-UHFFFAOYSA-N

InChI

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

SMILES string

N#Cc1c2ccccc2cc3ccccc13

assay

97%

form

powder

mp

173-177 °C (lit.)

functional group

nitrile

Quality Level

100

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This Item
45985227868851881
9-Anthracenecarbonitrile 97%

Sigma-Aldrich

152765

9-Anthracenecarbonitrile

9,10-Anthracenedicarbonitrile 97%

Sigma-Aldrich

459852

9,10-Anthracenedicarbonitrile

9-Anthracenecarboxaldehyde 97%

Sigma-Aldrich

278688

9-Anthracenecarboxaldehyde

9-cis-Astaxanthin analytical standard

Supelco

51881

9-cis-Astaxanthin

assay

97%

assay

97%

assay

97%

assay

≥90.0% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

-

Quality Level

100

form

powder

form

-

form

solid

form

-

mp

173-177 °C (lit.)

mp

340 °C (lit.)

mp

103-105 °C (lit.)

mp

-

functional group

nitrile

functional group

nitrile

functional group

aldehyde

functional group

-

General description

The fluorescence excitation spectra of 9-anthracenecarbonitrile has been studied[1].

Application

9-Anthracenecarbonitrile was used to study the mechanism of charge separation within phenothiazine (PTZH) or phenoxazine (PXZH), and 9-cyanoanthracene(electron acceptor)[2].

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB0994
STBL0940
STBH1859
STBH1994
51018MM

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T Hiratsuka
The Journal of biological chemistry, 265(31), 18786-18790 (1990-11-05)
A fluorophore, 9-anthroyl (AN) group, was covalently incorporated into the 23-kDa NH2-terminal peptide segment of myosin subfragment-1 (S-1) (Hiratsuka, T. (1989) J. Biol. Chem. 264, 18188-18194). The fluorescent S-1 derivative (AN-S-1) was utilized to detect conformational changes in the 23-kDa
T Hiratsuka
The Journal of biological chemistry, 265(31), 18791-18796 (1990-11-05)
In order to study the conformational changes associated with formation of the stable ternary complex of myosin subfragment-1 (S-1) with ADP and orthovanadate (Vi), S-1 was fluorescently labeled with 9-anthroylnitrile, 4-fluoro-7-nitrobenz-2-oxa-1,3-diazole, and 5-(iodoacetamido) fluorescein at the 23-, 50-, and 20-kDa
Barbara Pliszka et al.
Biochimica et biophysica acta, 1699(1-2), 201-205 (2004-05-26)
The fluorescent probe, 9-anthroylnitrile (ANN), can selectively attach to Ser-180 at the ATP-binding site of subfragment 1 (S1) of skeletal muscle myosin [J. Biol. Chem. 278 (2003) 31891]. We have found that MgATP, MgATPgammaS, MgADP.AlF(4) or MgPP(i), but not MgADP
M Takahashi et al.
Journal of pharmaceutical and biomedical analysis, 14(11), 1579-1584 (1996-08-01)
9-Anthroylnitrile was used as an achiral reagent for the derivatization of carnitine. The reagent forms UV-absorbing derivatives with the hydroxyl groups of carnitine enantiomers under very mild conditions. The derivatives were separated by high-performance liquid chromatography on an ovomucoid-conjugated column
K H Kim et al.
Archives of pharmacal research, 21(6), 651-656 (1998-12-30)
A sensitive high-performance liquid chromatographic (HPLC) method for the determination of aloesin in plasma was developed. After solid-phase extraction from plasma and derivatization of aloesin and compound AD-1, which was prepared from aloesin as a internal standard, with 9-anthroylnitrile in
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