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45789

Supelco

Indan

analytical standard

Sinónimos:

Hydrindene

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About This Item

Fórmula empírica (notación de Hill):
C9H10
Número de CAS:
496-11-7
Peso molecular:
118.18
Beilstein/REAXYS Number:
1904376
EC Number:
207-814-7
MDL number:
MFCD00003795
UNSPSC Code:
41116107
PubChem Substance ID:
329756953
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

C1Cc2ccccc2C1

InChI

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

InChI key

PQNFLJBBNBOBRQ-UHFFFAOYSA-N

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.

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pictograms

FlameHealth hazard
GHS02,GHS08

signalword

Danger

hcodes

H226,H304

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

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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Certificados de análisis (COA)

Lot/Batch Number
BCCK0746
BCBZ5252
SZBE261XV
SZBD186XV
SZBB343XV

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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.
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
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
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
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