Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

I2800

Sigma-Aldrich

Indene

contains 50-100 ppm tert-butylcatechol as stabilizer, technical grade, ≥90%

Sinonimo/i:

Indonaphthene

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Formula empirica (notazione di Hill):
C9H8
Numero CAS:
Peso molecolare:
116.16
Beilstein:
635873
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Grado

technical grade

Livello qualitativo

Saggio

≥90%

Forma fisica

liquid

contiene

50-100 ppm tert-butylcatechol as stabilizer

Indice di rifrazione

n20/D 1.595 (lit.)

P. eboll.

181-182 °C (lit.)

Punto di fusione

−5-−3 °C (lit.)

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

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Categorie correlate

Pittogrammi

FlameHealth hazard

Avvertenze

Danger

Indicazioni di pericolo

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’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

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
Song Tu et al.
Journal of agricultural and food chemistry, 56(13), 5247-5253 (2008-06-13)
Nineteen novel indene-substituted oxime ether strobilurins, which used an indene group to stabilize the ( E)-styryl group in SYP-Z071 (an unsaturated oxime strobilurin fungicide under development by the Shenyang Research Institute of Chemical Industry), were designed and synthesized. The biological
Hiroaki Kurouchi et al.
Journal of the American Chemical Society, 132(2), 807-815 (2009-12-19)
The chemical features, such as substrate stability, product distribution, and substrate generality, and the reaction mechanism of Brønsted superacid-catalyzed cyclization reactions of aromatic ring-containing acetoacetates (beta-ketoesters) were examined in detail. While two types of carbonyl cyclization are possible, i.e., keto
Ermitas Alcalde et al.
Organic & biomolecular chemistry, 6(20), 3795-3810 (2008-10-10)
A series of novel indene derivatives designed by a scaffold selection gave access to several examples of (Z)-arylmethylideneindenes and indenylsulfonamides that acted as serotonin 5-HT(6) receptor ligands. Different synthetic multistep routes could be applied to these target compounds, each with
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

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.