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45789

Supelco

Indan

analytical standard

Synonym(e):

Hydrinden

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About This Item

Empirische Formel (Hill-System):
C9H10
CAS-Nummer:
496-11-7
Molekulargewicht:
118.18
Beilstein:
1904376
EG-Nummer:
207-814-7
MDL-Nummer:
MFCD00003795
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756953

Qualität

analytical standard

Qualitätsniveau

100

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

n20/D 1.537 (lit.)

bp

176 °C (lit.)

mp (Schmelzpunkt)

−51 °C (lit.)

Dichte

0.965 g/mL at 25 °C (lit.)

Anwendung(en)

environmental

Format

neat

SMILES String

C1Cc2ccccc2C1

InChI

1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2

InChIKey

PQNFLJBBNBOBRQ-UHFFFAOYSA-N

Angaben zum Gen

human ... CYP1A2(1544)

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Anwendung

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

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Piktogramme

FlameHealth hazard
GHS02,GHS08

Signalwort

Danger

H-Sätze

H226 - H304

Gefahreneinstufungen

Asp. Tox. 1 - Flam. Liq. 3

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

129.2 °F - closed cup

Flammpunkt (°C)

54 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCK0746
BCBZ5252
SZBE261XV
SZBD186XV
SZBB343XV

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Die Dokumentenbibliothek aufrufen

Stuart N L Bennett et al.
Bioorganic & medicinal chemistry letters, 20(12), 3511-3514 (2010-05-25)
A series of carboxylic acid glycogen phosphorylase inhibitors, which have potential as oral antidiabetic agents, is described. Defining and applying simple physicochemical design criteria was used to assess the opportunity and to focus synthetic efforts on compounds with the greatest
Michael F Gross et al.
Bioorganic & medicinal chemistry letters, 17(10), 2849-2853 (2007-03-14)
A collection of aryl sulfonamido indanes based on the lead compound 1 was synthesized and evaluated for Kv1.5 inhibitory activity. Kv1.5 inhibitors have the potential to be atrium-selective agents for treatment of atrial fibrillation. (1R,2R)-1 has an IC(50) of 0.033microM
Tong-Xin Liu et al.
Organic letters, 13(22), 6130-6133 (2011-10-29)
The addition of aluminum chloride to the manganese acetate-mediated radical reaction of [60]fullerene with 2-arylmalonates, 2-benzylmalonates, and 2-arylcyanoacetates can switch the reaction pathway and affords a variety of structurally novel and scarce [60]fullerene-fused tetrahydronaphthalene and indane derivatives. These products are
Christopher S Frampton et al.
Acta crystallographica. Section C, Crystal structure communications, 68(Pt 8), o323-o326 (2012-08-02)
The title molecular salt, C(8)H(12)N(+)·C(26)H(21)O(3)(-), contains a dimeric indane pharmacophore that demonstrates potent anti-inflammatory activity. The indane group of the anion exhibits some disorder about the α-C atom, which appears common to many structures containing this group. A model to
Yuka Kobayashi et al.
Chirality, 17(2), 108-112 (2005-01-22)
Both novel enantiopure trans-1-aminobenz[f]indan-2-ols (4) were obtained from the racemate by the diastereomeric salt formation with (+)- and (-)-dibenzoyltartaric acids (8), respectively, and the absolute configuration of the enantiomer 4 in the less-soluble diastereomeric salt of racemic 4 with (+)-8
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