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Documenti

168769

Sigma-Aldrich

Indene

98%

Sinonimo/i:

Indonaphthene

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About This Item

Formula empirica (notazione di Hill):
C9H8
Numero CAS:
95-13-6
Peso molecolare:
116.16
Beilstein:
635873
Numero CE:
202-393-6
Numero MDL:
MFCD00003777
Codice UNSPSC:
12352100
eCl@ss:
39011614
ID PubChem:
24850253
NACRES:
NA.22

Saggio

98%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.595 (lit.)

P. eboll.

181-182 °C (lit.)

Punto di fusione

−5-−3 °C (lit.)

Solubilità

organic solvents: miscible
water: insoluble

Densità

0.996 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

C1C=Cc2ccccc12

InChI

1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
YBYIRNPNPLQARY-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Indene is oxidized to mixtures of cis- and trans-indandiols and related metabolites by Pseudomonas putida and Rhodococcus sp.

Applicazioni

Indene was used in the synthesis of new C60 derivative, indene-C60 bisadduct. It was used in preparing polyindene by the controlled cationic polymerization initiated with cumyl methyl ether/TiCl4 in CH2Cl2.

Pittogrammi

FlameHealth hazard
GHS02,GHS08

Avvertenze

Danger

Indicazioni di pericolo

H226,H304

Classi di pericolo

Asp. Tox. 1 - Flam. Liq. 3

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

136.4 °F - closed cup

Punto d’infiammabilità (°C)

58 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Sigma-Aldrich

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Sigma-Aldrich

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Dicyclopentadiene contains BHT as stabilizer

Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

393231

Dichloro[rac-ethylenebis(indenyl)]zirconium(IV)

High glass transition temperature polyolefins obtained by the catalytic hydrogenation of polyindene.
Hahn SF and Hillmyer MA.
Macromolecules, 36(1), 71-76 (2003)
B C Buckland et al.
Metabolic engineering, 1(1), 63-74 (2000-08-10)
Indene is oxidized to mixtures of cis- and trans-indandiols and related metabolites by Pseudomonas putida and Rhodococcus sp. isolates. Indene metabolism is consistent with monooxygenase and dioxygenase activity. P. putida resolves enantiomeric mixtures of cis-1,2-indandiol by further selective oxidation of
Ermitas Alcalde et al.
Journal of medicinal chemistry, 52(3), 675-687 (2009-01-23)
Scaffold selection involving an indole-to-indene core change led to the discovery of a series of indenylsulfonamides that act as 5-HT6 serotonin receptor agonists. The variety of the targeted ligands and their synthetic complexity required multistep synthetic approaches. The novel indenylsulfonamides
Helga Seyler et al.
The Journal of organic chemistry, 76(9), 3551-3556 (2011-03-12)
Various fullerene-based electron acceptor materials for organic photovoltaic applications were prepared via [3+2] and [4+2] cycloadditions using a continuous flow approach. The 1,3-dipolar cycloaddition of the tosylhydrazone precursor and the Diels-Alder cycloaddition of indene to either C(60) or C(70) under
Ram Shankar Upadhayaya et al.
Organic & biomolecular chemistry, 8(24), 5661-5673 (2010-10-12)
Prompted by our discovery of a new class of conformationally-locked indeno[2,1-c]quinolines as anti-mycobacterials, compounds 2a and 3a (Fig. 1; MIC < 0.39 μg mL(-1) and 0.78 μg mL(-1), respectively)(14) with a freely rotating C2-imidazolo substituent, we herein describe the synthesis
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