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<compound>
  <id type="integer">6138</id>
  <title nil="true"/>
  <common-name>CIS-CARVONE OXIDE</common-name>
  <description>CIS-CARVONE OXIDE belongs to the oxepanes, a class of organoheterocyclic compounds within the organic compounds. This compound has the formula C10H14O2 and an average molecular weight of 166.22 g/mol. In industrial applications, it serves as a flavouring agent and a nutrient.</description>
  <cas>18383-49-8</cas>
  <pubchem-id>11030188</pubchem-id>
  <chemical-formula>C10H14O2</chemical-formula>
  <weight nil="true"/>
  <appearance nil="true"/>
  <melting-point nil="true"/>
  <boiling-point nil="true"/>
  <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 nil="true"/>
  <use-source nil="true"/>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2016-05-19T01:57:30Z</created-at>
  <updated-at type="dateTime">2026-04-06T14:14:12Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id nil="true"/>
  <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>[H][C@]12C[C@]([H])(CC(=O)[C@@]1(C)O2)C(C)=C</moldb-smiles>
  <moldb-formula>C10H14O2</moldb-formula>
  <moldb-inchi>InChI=1S/C10H14O2/c1-6(2)7-4-8(11)10(3)9(5-7)12-10/h7,9H,1,4-5H2,2-3H3/t7-,9-,10+/m0/s1</moldb-inchi>
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  <moldb-average-mass type="decimal">166.22</moldb-average-mass>
  <moldb-mono-mass type="decimal">166.099379691</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp nil="true"/>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id nil="true"/>
  <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 nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM005033</chemdb-id>
  <dsstox-id>DTXSID60171487</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00127656</susdat-id>
  <iupac nil="true"/>
  <moldb-polar-surface-area>29.6</moldb-polar-surface-area>
  <moldb-refractivity>45.78</moldb-refractivity>
  <moldb-polarizability>18.31664294169165</moldb-polarizability>
  <moldb-rotatable-bond-count>1</moldb-rotatable-bond-count>
  <moldb-acceptor-count>2</moldb-acceptor-count>
  <moldb-donor-count>0</moldb-donor-count>
  <moldb-pka-strongest-acidic>18.837998275660137</moldb-pka-strongest-acidic>
  <moldb-pka-strongest-basic>-4.28042857212882</moldb-pka-strongest-basic>
  <moldb-physiological-charge>0</moldb-physiological-charge>
  <moldb-number-of-rings>2</moldb-number-of-rings>
  <moldb-alogps-logp>1.29</moldb-alogps-logp>
  <moldb-alogps-logs>-1.66</moldb-alogps-logs>
  <moldb-alogps-solubility>3.64e+00 g/l</moldb-alogps-solubility>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organoheterocyclic compounds</superklass>
  <klass>Oxepanes</klass>
  <subklass nil="true"/>
  <paper-count type="integer">33</paper-count>
  <sync-id>CED0026313</sync-id>
  <structure-inchikey>YGMNGQDLUQECTO-UJNFCWOMSA-N</structure-inchikey>
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</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T04:02:13Z</structure-indexed-at>
</compound>
