- Indene
Chembox new
ImageFile=Indene.png
ImageSize=150px
IUPACName=1H-indene
OtherNames=
Section1= Chembox Identifiers
CASNo=95-13-6
PubChem=7219
SMILES=C1C=CC2=CC=CC=C21
Section2= Chembox Properties
Formula=C9H8
MolarMass=116.16
Appearance=
Density=
MeltingPt=
BoilingPt=
Solubility=
Section3= Chembox Hazards
MainHazards=
FlashPt=
Autoignition=Indene is a
flammable polycyclichydrocarbon withchemical formula C9H8. It is composed of abenzene ring fused with acyclopentene ring and occurs as a colorless to pale yellow liquid. A principal industrial use of indene is in the production of indene/cumarone thermoplastic resins.It is also known as benzocyclopentadiene, and occurs naturally in
coal-tar fractions boiling around 175-185 °C. It can be obtained from this fraction by heating withsodium (indene is acidic), separating the solid sodio-indene, and recovering by steam distilling it.Indene readily polymerises. Oxidation of indene with acid
dichromate yieldshomophthalic acid .It condenses with
ethyl oxalate in the presence ofsodium ethoxide to form indene-oxalic ester, and with aldehydes or ketones in the presence ofalkali to form benzofulvenes. The latter are highly coloured.See also
*
Indane
*Indole
*Isoindene References
*cite journal
title = Zur Synthese von Indenderivaten
author = W. v. Miller, Rohde
journal = Berichte der deutschen chemischen Gesellschaft
volume = 22
issue = 2
pages = 1881–1886
year = 1889
doi = 10.1002/cber.18890220227
*cite journal
title = Zur Synthese von Indenderivaten
author = W. v. Miller, Rohde
journal = Berichte der deutschen chemischen Gesellschaft
volume = 23
issue = 2
pages = 1881–1886
year = 1890
doi = 10.1002/cber.18900230228
*cite journal
title = Zur Synthese von Indenderivaten
author = W. v. Miller, Rohde
journal = Berichte der deutschen chemischen Gesellschaft
volume = 23
issue = 2
pages = 1887–1902
year = 1890
doi = 10.1002/cber.18900230227
*cite book
title = Organic Chemistry
last = Finar
first = I. L.
publisher = Longman Scientific & Technical
isbn = 0582442575
date = 1985
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