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48568

Supelco

Fluorene

analytical standard

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About This Item

Formule empirique (notation de Hill):
C13H10
Numéro CAS:
86-73-7
Poids moléculaire :
166.22
Beilstein:
1363491
Numéro CE :
201-695-5
Numéro MDL:
MFCD00001111
Code UNSPSC :
12000000
ID de substance PubChem :
24872116
Le tarif et la disponibilité ne sont pas disponibles actuellement.

Qualité

analytical standard

Niveau de qualité

100

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 5000 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

pb

298 °C (lit.)

Pf

111-114 °C (lit.)

Application(s)

environmental

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

C1c2ccccc2-c3ccccc13

InChI

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

Clé InChI

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.[1]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

Environment
GHS09

Mention d'avertissement

Warning

Mentions de danger

H410

Conseils de prudence

P273 - P391 - P501

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

303.8 °F - closed cup

Point d'éclair (°C)

151.0 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
LC26573V
LC24997V
LC18983V
LC08752V
LC05789V

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Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

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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
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
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
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
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