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文件

N10209

9-硝基蒽

Name: 9-硝基蒽
Brand: ALDRICH

93%

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经验公式（希尔记法）:

C₁₄H₉NO₂

CAS号:

602-60-8

分子量:

223.23

Beilstein:

1877509

EC 号:

210-021-9

MDL编号:

MFCD00001248

PubChem化学物质编号:

24897455

NACRES:

NA.22

质量水平

100

检测方案

93%

形式

powder

mp

141-144 °C (lit.)

SMILES字符串

[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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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

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One-step synthesis of [16]helicene.

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

High Fluorescent Porphyrin-PAMAM-Fluorene Dendrimers.

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)

HPLC retention behavior of poly-aromatic-hydrocarbons on aminopropyl silica gels modified with Cu(II)- and Ni(II)-phthalocyanine derivatives in non-polar eluent.

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

The preparation of anthraquinone used in the National Toxicology Program cancer bioassay was contaminated with the mutagen 9-nitroanthracene.

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

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