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Merck
CN

45789

Indan

analytical standard

Synonym(s):

Hydrindene

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About This Item

Empirical Formula (Hill Notation):
C9H10
CAS Number:
496-11-7
Molecular Weight:
118.18
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756953
EC Number:
207-814-7
Beilstein/REAXYS Number:
1904376
MDL number:
MFCD00003795

Key Documents

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Product Name

Indan, analytical standard

InChI key

PQNFLJBBNBOBRQ-UHFFFAOYSA-N

InChI

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

SMILES string

C1Cc2ccccc2C1

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.537 (lit.)

bp

176 °C (lit.)

mp

−51 °C (lit.)

density

0.965 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

Quality Level

100

Gene Information

human ... CYP1A2(1544)

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Application

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

Other Notes

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.

pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Danger

hcodes

H226,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCK0746
BCBZ5252

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Wei Li et al.
Chemical communications (Cambridge, England), 46(22), 3979-3981 (2010-04-22)
(S,R)-Indan-ambox ligand and its ruthenium(II) complex have been prepared and successfully applied to asymmetric hydrogenation of prochiral simple ketones. A wide range of unfunctionalized ketones are reduced by Ru(II)-indan-ambox catalyst with excellent enantioselectivities (up to 97% ee).
Kenji Kabashima et al.
FEBS letters, 578(1-2), 36-40 (2004-12-08)
Nuclear factor kappa B (NF-kappaB) plays a wide variety of pathophysiological roles and modulation of its pathway can be a good novel drug target. Here, we found that our recently synthesized NF-kappaB inhibitor attenuated an ovalbumin-specific delayed-type hypersensitivity response in
Peter R Andreana et al.
Organic letters, 6(23), 4231-4233 (2004-11-05)
A catalytic asymmetric Passerini reaction using tridentate indan (pybox) Cu(II) Lewis acid complex 4 with substrates capable of bidentate coordination has been achieved. The reaction occurs via ligand-accelerated catalysis.
Naoki Tarui et al.
Bioscience, biotechnology, and biochemistry, 66(2), 464-466 (2002-05-10)
Racemic indan derivatives have been resolved by the hydrolysis of amide bonds using Corynebacterium ammoniagenes IFO12612 to produce (S)-amine and (R)-amides. In the kinetic resolution of 1 (N-12-(6-methoxy-indan-1-yl)ethyl]acetamide), it was possible to run the reaction to 44% conversion on a
Manoranjan Adak et al.
Nepal Medical College journal : NMCJ, 8(1), 22-26 (2006-07-11)
To study the hyoplipidemic activity of non-methoxy and methoxy substituted--alkyl indan acetic acids in normogenic and hypergenic animal models. The hyoplipidemic activity was evaluated using normogenic and hypergenic rat models. Indan acids synthesized in our laboratory (50 mg/kg) and the
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