I2304
1-Indanone
ReagentPlus®, ≥99%
Synonym(s):
1-Oxoindane, α-Hydrindone
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About This Item
Empirical Formula (Hill Notation):
C9H8O
CAS Number:
Molecular Weight:
132.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-470-1
Beilstein/REAXYS Number:
507957
MDL number:
Assay:
≥99%
Quality Level
product line
ReagentPlus®
assay
≥99%
bp
243-245 °C (lit.)
mp
38-40 °C (lit.)
density
1.103 g/mL at 25 °C (lit.)
SMILES string
O=C1CCc2ccccc12
InChI
1S/C9H8O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4H,5-6H2
InChI key
QNXSIUBBGPHDDE-UHFFFAOYSA-N
Application
1-Indanone can be used to synthesize:
It can also be used to build other indan-based systems like truxene, prekinamycin, indan-C60 and biindanylidenes.
- 11H-Indeno-[1,2-b]-quinolin-10-ylamine, a potential acetylcholinesterase inhibitor for the treatment of Alzheimer′s disease.
- CoumBARAC (coumarin fused biarylazacyclooctynone) for fluorogenic real-time imaging of azide-labeled biomolecules.
- Light emitting, organic semiconductors such as 4-pyrenyl-2-piperidin-1-yl-9H-fluorene-1-carbonitrile and bisindenoanthrazolines for organic light emitting diode (OLED) applications.
It can also be used to build other indan-based systems like truxene, prekinamycin, indan-C60 and biindanylidenes.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
233.0 °F - closed cup
flash_point_c
111.67 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Trisannulated benzene derivatives by acid catalyzed aldol cyclotrimerizations of cyclic ketones. Methodology development and mechanistic insight.
Amick AW and Scott LT.
The Journal of Organic Chemistry, 72(9), 3412-3418 (2007)
Novel n-type conjugated ladder heteroarenes: Synthesis, self-assembly of nanowires, electron transport, and electroluminescence of bisindenoanthrazolines.
Ahmed E, et al.
Chemistry of Materials, 22(20), 5786-5796 (2010)
Biindanylidenes: role of central bond torsion in nonvertical triplet excitation transfer to the stilbenes.
Saltiel J, et al.
Journal of the American Chemical Society, 125(52), 16158-16159 (2003)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| I2304-100G | 04061832490212 |
| I2304-25G | 04061833848418 |
| I2304-10G | 04061832490229 |