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Merck

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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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

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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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK0746
BCBZ5252

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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
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
Konstantin Ulanenko et al.
The Journal of organic chemistry, 71(18), 7053-7056 (2006-08-26)
5-Dimethylamino-1-aminoindan undergoes thermal decomposition and reacts with 6-chlorouracil to give 5-indanyl-6-chlorouracil derivative 9. The formation of 9 may be rationalized by a putative mechanism based on the intermediacy of the imminium methide species 8a.
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
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
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