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48568

Supelco

Fluorene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C13H10
CAS Number:
Molecular Weight:
166.22
Beilstein:
1363491
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 5000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

298 °C (lit.)

mp

111-114 °C (lit.)

application(s)

environmental

format

neat

storage temp.

2-30°C

SMILES string

C1c2ccccc2-c3ccccc13

InChI

1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2

InChI key

NIHNNTQXNPWCJQ-UHFFFAOYSA-N

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Application

Fluorene has been used as a test material in studying its electronic transitions in gas and crystalline phases, and in stretched polymer sheets, measured with synchrotron radiation.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

303.8 °F - closed cup

Flash Point(C)

151.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Electronic transitions of fluorene, dibenzofuran, carbazole, and dibenzothiophene: From the onset of absorption to the ionization threshold.
Nguyen D D, et al.
Journal of Molecular Spectroscopy, 264(1), 19-25 (2010)
Le Bao et al.
The Analyst, 137(17), 4010-4015 (2012-07-12)
This work aims at the development of a fast scanning method for organic pollutants with low-cost small Raman spectrometers. A gold nanoparticles-embedded alginate gel is prepared and applied as the substrate for surface enhanced Raman spectrometric detection of polycyclic aromatic
Ute B Cappel et al.
Nano letters, 12(9), 4925-4931 (2012-08-24)
Solid state dye-sensitized solar cells (sDSCs) employing the hole conductor 2,2'7,7'-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9'-spirobifluorene (spiro-MeOTAD) require the presence of oxygen during fabrication and storage. In this paper, we determine the concentrations of oxidized spiro-MeOTAD within devices under different operating and storage conditions by
Michèle J Régimbald-Krnel et al.
The Journal of organic chemistry, 78(17), 8789-8795 (2013-08-15)
Diphenylcarbene (DPC) generated by high-intensity laser photolysis of diphenyldiazomethane rearranges to fluorene (FL) by two distinct mechanisms as revealed by methyl-group labeling. Thus, excimer laser irradiation of p,p'-dimethyldiphenyldiazomethane generates 3,6-dimethylfluorene (3,6-DMF) and 2,7-dimethylfluorene (2,7-DMF), which were identified by fluorescence measurements
Yoshiaki Amatatsu
The journal of physical chemistry. A, 116(41), 10182-10193 (2012-09-25)
A fluorene-based light-driven molecular rotary motor with constant rotation has been designed by means of ab initio molecular orbital calculations. A model molecule is obtained by a chemical modification of 9-(5-methyl-2-phenyl-2-cyclopenten-1-ylidene)-9H-fluorene (MPCPF) which we reported recently. Despite that MPCPF has

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