<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-06 08:15:30 UTC</creation_date>
  <update_date>2026-04-16 22:49:17 UTC</update_date>
  <accession/>
  <common_name>Syn-Dechlorane Plus</common_name>
  <class>SmallMolecule</class>
  <description>Syn-Dechlorane Plus (C18H12Cl12) is an organohalogen compound. Syn-Dechlorane Plus belongs to the vinyl chlorides, a subclass of vinyl halides within the organic compounds. With an average molecular weight of 653.69 g/mol, Syn-Dechlorane Plus is a heavy molecule. This substance has been found in or released from one recorded source: indoor air, dust, and atmospheric transport. The recorded exposure route for this compound is inhalation.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>(1R,2R,5S,6S,9R,10R,13S,14S)-1,6,7,8,9,14,15,16,17,17,18,18-Dodecachloropentacyclo[12.2.1.16,9.02,13.05,10]octadeca-7,15-diene</synonym>
    <synonym>(1R,2R,5S,6S,9R,10R,13S,14S)-1,6,7,8,9,14,15,16,17,17,18,18-Dodecachlorpentacyclo[12.2.1.16,9.02,13.05,10]octadeca-7,15-dien</synonym>
    <synonym>1,4:7,10-Dimethanodibenzo[a,e]cyclooctene, 1,2,3,4,7,8,9,10,13,13,14,14-dodecachloro-1,4,4a,5,6,6a,7,10,10a,11,12,12a-dodecahydro-, (1R,4S,4aS,6aR,7R,10S,10aS,12aR)-</synonym>
    <synonym>DECHLORANE PLUS SYN</synonym>
    <synonym>DODECACHLOROPENTACYCLOOCTADECADIENE, SYN-</synonym>
    <synonym>syn-dodecachloropentacyclooctadecadiene</synonym>
  </synonyms>
  <chemical_formula>C18H12Cl12</chemical_formula>
  <average_molecular_weight>653.69</average_molecular_weight>
  <monisotopic_moleculate_weight>647.720133</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>135821-03-3</cas_registry_number>
  <smiles>C1CC2C(CCC3C1C4(C(=C(C3(C4(Cl)Cl)Cl)Cl)Cl)Cl)C5(C(=C(C2(C5(Cl)Cl)Cl)Cl)Cl)Cl</smiles>
  <inchi>InChI=1S/C18H12Cl12/c19-9-10(20)15(25)7-3-4-8-6(2-1-5(7)13(9,23)17(15,27)28)14(24)11(21)12(22)16(8,26)18(14,29)30/h5-8H,1-4H2/t5-,6+,7+,8-,13-,14+,15+,16-</inchi>
  <inchikey>UGQQAJOWXNCOPY-MXYLTYEXSA-N</inchikey>
  <taxonomy>
    <kingdom/>
    <super_class/>
    <class/>
    <sub_class/>
    <direct_parent/>
    <alternate_parents/>
    <substituents/>
    <molecular_framework/>
    <descriptors/>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways/>
  <state/>
  <appearance/>
  <experimental_properties/>
  <predicted_properties>
    <property>
      <kind>average_mass</kind>
      <value>653.69</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>647.720133</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>C1CC2C(CCC3C1C4(C(=C(C3(C4(Cl)Cl)Cl)Cl)Cl)Cl)C5(C(=C(C2(C5(Cl)Cl)Cl)Cl)Cl)Cl</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C18H12Cl12</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C18H12Cl12/c19-9-10(20)15(25)7-3-4-8-6(2-1-5(7)13(9,23)17(15,27)28)14(24)11(21)12(22)16(8,26)18(14,29)30/h5-8H,1-4H2/t5-,6+,7+,8-,13-,14+,15+,16-</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>UGQQAJOWXNCOPY-MXYLTYEXSA-N</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
  <route_of_exposure/>
  <mechanism_of_toxicity/>
  <metabolism/>
  <toxicity/>
  <lethaldose/>
  <carcinogenicity/>
  <use_source/>
  <min_risk_level/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f726c7a5658&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id/>
  <hmdb_id/>
  <pubchem_compound_id>14178853</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>52083826</chemspider_id>
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  <biocyc_id/>
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  <wikipidia/>
  <general_references/>
  <targets>
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</compound>
