<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4874</id>
  <title>T3D4819</title>
  <common-name>Indene</common-name>
  <description>Indene is a flammable polycyclic hydrocarbon. It is composed of a benzene ring fused with a cyclopentene ring. This aromatic liquid is colorless although samples often are pale yellow. The principal industrial use of indene is in the production of indene/coumarone thermoplastic resins.</description>
  <cas>95-13-6</cas>
  <pubchem-id>7219</pubchem-id>
  <chemical-formula>C9H8</chemical-formula>
  <weight nil="true"/>
  <appearance></appearance>
  <melting-point>-1.8°C</melting-point>
  <boiling-point>182°C</boiling-point>
  <density nil="true"/>
  <solubility nil="true"/>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>It is composed of a benzene ring fused with a cyclopentene ring.</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2014-09-11T05:17:58Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:26:57Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Indene</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C11565</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>33051</chebi-id>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB02815</drugbank-id>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>C1C=CC2=CC=CC=C12</moldb-smiles>
  <moldb-formula>C9H8</moldb-formula>
  <moldb-inchi>InChI=1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2</moldb-inchi>
  <moldb-inchikey>InChIKey=YBYIRNPNPLQARY-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">116.1598</moldb-average-mass>
  <moldb-mono-mass type="decimal">116.062600256</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Liquid</state>
  <logp>2.92</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id>6949</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference>&lt;p&gt;Hisatake Sato, Masaharu Makino, &amp;#8220;Method for preparing light-colored indene-coumarone resin.&amp;#8221; U.S. Patent US4946915, issued July, 1930.&lt;/p&gt;</synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
