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Merck

48568

Fluorene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C13H10
CAS Number:
86-73-7
Molecular Weight:
166.22
EC Number:
201-695-5
UNSPSC Code:
12352200
PubChem Substance ID:
24872116
Beilstein/REAXYS Number:
1363491
MDL number:
MFCD00001111
NACRES:
NA.24

Key Documents

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InChI key

NIHNNTQXNPWCJQ-UHFFFAOYSA-N

InChI

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

SMILES string

C1c2ccccc2-c3ccccc13

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

Quality Level

100

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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
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

flash_point_f

303.8 °F - closed cup

flash_point_c

151.0 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
LRAE0774
LRAD5994
LRAC8730
LRAC7242
LRAC4033

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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)
Pierre Lovera et al.
Journal of nanoscience and nanotechnology, 13(7), 5194-5202 (2013-08-02)
Organic nanowires based on a fluorene homopolymer and a copolymer, i.e., poly(9,9-dioctylfluorene), F8, and poly(9,9-dioctylfluorene-co-benzothiadiazole), F8BT, respectively, were synthesised by solution assisted wetting of porous anodic alumina templates. Nanowires ranged between 3 microm and 50 microm in length, and were
S A Schmid et al.
Philosophical transactions. Series A, Mathematical, physical, and engineering sciences, 370(1972), 3787-3801 (2012-07-04)
We have investigated the energy transfer dynamics in a supramolecular linear polymer chain comprising oligofluorene (OF) energy donor units linked by quadruple hydrogen-bonding groups, and oligophenylene (OPV) chain ends that act as energy acceptors. Using femtosecond spectroscopy, we followed the
Shuying Ma et al.
Chemical communications (Cambridge, England), 48(97), 11847-11849 (2012-11-02)
A novel 3D donor material (SF8TBT) based on spiro-fluorene has been developed. Compared with the corresponding 1D linear molecule, the OPVs of this 3D donor exhibited power conversion efficiencies of 4.82%, much higher than that of 1D small molecules (1.69%).
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
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