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N10209

Sigma-Aldrich

9-Nitroanthracene

93%

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About This Item

Empirical Formula (Hill Notation):
C14H9NO2
CAS Number:
602-60-8
Molecular Weight:
223.23
Beilstein:
1877509
EC Number:
210-021-9
MDL number:
MFCD00001248
UNSPSC Code:
12352100
PubChem Substance ID:
24897455
NACRES:
NA.22

Quality Level

100

Assay

93%

form

powder

mp

141-144 °C (lit.)

SMILES string

[O-][N+](=O)c1c2ccccc2cc3ccccc13

InChI

1S/C14H9NO2/c16-15(17)14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9H

InChI key

LSIKFJXEYJIZNB-UHFFFAOYSA-N

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Related Categories

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Karla I Garfias-Gonzalez et al.
Molecules (Basel, Switzerland), 20(5), 8548-8559 (2015-05-20)
Two new classes of dendrimers bearing 8 and 32 fluorene donor groups have been synthesized. The first and second generations of these porphyrin-PAMAM-fluorene dendrimers were characterized by 1H-NMR, 13C-NMR, FTIR, UV-vis spectroscopy, elemental analyses and MALDI-TOF mass spectrometry. The UV-vis
Application of 9-nitroanthracene as a matrix for laser desorption/ionization analysis of fluorinated fullerenes.
Alexey V Streletskiy et al.
Rapid communications in mass spectrometry : RCM, 18(3), 360-362 (2004-02-03)
B E Butterworth et al.
Mutagenesis, 16(2), 169-177 (2001-03-07)
Commercial anthraquinone (AQ) (9,10-anthracenedione) is produced by at least three different production methods worldwide: oxidation of anthracene (AQ-OX), Friedel-Crafts technology (AQ-FC) and by Diels-Alder chemistry (AQ-DA), with the final product varying in color and purity. AQ-OX begins with anthracene produced
Hiromichi Akizawa et al.
Chemical & pharmaceutical bulletin, 52(1), 41-46 (2004-01-08)
A comparative study was conducted to elucidate the mechanism underlying the separation of poly-aromatic-hydrocarbons (PAHs) and related compounds thereof on a column packed with silica gels modified with Ni(II)- or Cu(II)-phthalocyanine derivatives (PCS) (Ni- or Cu-PCS(D) column) and commercially available
Kazuyuki Mori et al.
Angewandte Chemie (International ed. in English), 54(23), 6847-6851 (2015-04-25)
A single-strand arylene-vinylene precursor containing four phenylene and three naphthylene units linked together with six vinylene spacers undergoes helical folding via sextuple photocyclization to give a [16]helicene core in a single step. The phenylene and naphthylene units are arranged in
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