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%
InChI key
QNXSIUBBGPHDDE-UHFFFAOYSA-N
InChI
1S/C9H8O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4H,5-6H2
SMILES string
O=C1CCc2ccccc12
product line
ReagentPlus®
assay
≥99%
bp
243-245 °C (lit.)
Quality Level
density
1.103 g/mL at 25 °C (lit.)
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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
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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Indan-C 60: from a crystalline molecule to photovoltaic application.
Wang T, et al.
Chemical Communications (Cambridge, England), 49(85), 9923-9925 (2013)
Acetylcholinesterase inhibitors for potential use in Alzheimer's disease: molecular modeling, synthesis and kinetic evaluation of 11H-indeno-[1, 2-b]-quinolin-10-ylamine derivatives.
Rampa A, et al.
Bioorganic & Medicinal Chemistry, 8(3), 497-506 (2000)
Donor-acceptor 9-uncapped fluorenes and fluorenones as stable blue light emitters.
Goel A, et al.
Organic Letters, 11(6), 1289-1292 (2009)
Highly efficient phosphorescent light-emitting diodes by using an electron-transport material with high electron affinity.
Earmme T, et al.
The Journal of Physical Chemistry C, 113(43), 18448-18450 (2009)
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)
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