Key Documents

View All Documentation

N10209

9-Nitroanthracene

Name: 9-Nitroanthracene
Brand: ALDRICH

93%

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₁₄H₉NO₂

CAS Number:

602-60-8

Molecular Weight:

223.23

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24897455

EC Number:

210-021-9

Beilstein/REAXYS Number:

1877509

MDL number:

MFCD00001248

Assay:

93%

Form:

powder

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

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

Description

Still not finding the right product?

Explore all of our products under 9-Nitroanthracene

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

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

View All Related Papers

Global Trade Item Number

SKU	GTIN
N10209-5G	04061834093213
N10209-1G	04061838355157