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128333

Sigma-Aldrich

Fluorene

98%

Sinônimo(s):

2,2′-Methylenebiphenyl, Diphenylenemethane

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About This Item

Fórmula empírica (Notação de Hill):
C13H10
Número CAS:
86-73-7
Peso molecular:
166.22
Beilstein:
1363491
Número CE:
201-695-5
Número MDL:
MFCD00001111
Código UNSPSC:
12352100
ID de substância PubChem:
24847846
NACRES:
NA.22

Ensaio

98%

forma

chunks
crystalline powder
crystals
powder
solid

pb

298 °C (lit.)

pf

111-114 °C (lit.)

cadeia de caracteres 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

chave InChI

NIHNNTQXNPWCJQ-UHFFFAOYSA-N

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Descrição geral

Fluorene is a rigid, planar polycyclic aromatic hydrocarbon. White crystals of fluorene have violet fluorescence, from which its name derives. It is used as a precursor to other fluorene compounds. Fluorene is used as a chemical intermediate in the formation of polyradicals for resins as well as the manufacture of resinous products and dyes.

Aplicação

Fluorene was used study the extraction of specific, semiconducting single-wall carbon nanotubes (SWCNTs).

Características e benefícios

As a monomer, fluorene exhibits significant solubility while maintaining a high degree of delocalization.

Pictogramas

Environment
GHS09

Palavra indicadora

Warning

Frases de perigo

H410

Declarações de precaução

P273 - P391 - P501

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

303.8 °F - closed cup

Ponto de fulgor (°C)

151.0 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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8.03977

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Hexano anhydrous, 95%

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296090

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o-Toluic acid 99%

Sigma-Aldrich

T36404

o-Toluic acid

2-Chlorobenzoic acid 98%

Sigma-Aldrich

135577

2-Chlorobenzoic acid

9-Methyl-9H-fluorene AldrichCPR

Sigma-Aldrich

SYX00229

9-Methyl-9H-fluorene

Acenaphthene 99%

Sigma-Aldrich

215376

Acenaphthene

Light-emitting diodes based on fluorene polymers
Bernius M, et al.
Thin Solid Films, 363(1-2), 55-57 (2000)
Zhengcai Guo et al.
Bioelectrochemistry (Amsterdam, Netherlands), 135, 107552-107552 (2020-06-12)
Developing a cost-effective and simple micro-analysis tool has long been an important objective in the toxicological detection of fluorene. In this study, a disposable paper-based micro-analysis device (μ-PAD) was designed using graphite doped with multi-walled carbon nanotubes (MWCNTs) to hand
Synthesis and characterization of new imidazole and fluorene--bisphenol based polyamides: Thermal, photophysical and antibacterial properties
Ghaemy M, et al.
Reactive and Functional Polymers, 73(3), 555-563 (2013)
Masayoshi Tange et al.
Nanoscale, 6(1), 248-254 (2013-11-05)
To understand how fluorene-based polymers selectively extract specific semiconducting single-wall carbon nanotubes (SWCNTs), we compared the optical transitions of SWCNTs wrapped with poly(9,9-dioctylfluorene-alt-pyridine) (PFOPy), i.e., structure-selective polymers, with those wrapped with poly(9,9-di-n-dodecylfluorene) (PFD), i.e., non-selective polymers, in organic solvents by
Willian G Birolli et al.
Marine pollution bulletin, 129(2), 525-533 (2017-10-23)
The biodegradation of polycyclic aromatic hydrocarbons (PAHs) by marine-derived fungi was reported in this work. Marine-derived fungi (Trichoderma harzianum CBMAI 1677, Cladosporium sp. CBMAI 1237, Aspergillus sydowii CBMAI 935, Penicillium citrinum CBMAI 1186 and Mucor racemosus CBMAI 847) biodegraded anthracene
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