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<compound>
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  <common-name>4-dimethoxyphosphinothioyloxy-3-methoxybenzonitrile</common-name>
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  <pubchem-id>77128</pubchem-id>
  <chemical-formula>C10H12NO4PS</chemical-formula>
  <weight>273.25</weight>
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  <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">2026-08-26T17:56:17Z</created-at>
  <updated-at type="dateTime">2026-08-26T17:56:17Z</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"/>
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  <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>COC1=C(C=CC(=C1)C#N)OP(=S)(OC)OC</moldb-smiles>
  <moldb-formula>C10H12NO4PS</moldb-formula>
  <moldb-inchi>InChI=1S/C10H12NO4PS/c1-12-10-6-8(7-11)4-5-9(10)15-16(17,13-2)14-3/h4-6H,1-3H3</moldb-inchi>
  <moldb-inchikey>JFEUEPKNHJHJDY-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal" nil="true"/>
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  <origin nil="true"/>
  <state nil="true"/>
  <logp>2.8</logp>
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  <structure-image-content-type nil="true"/>
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  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM273896</chemdb-id>
  <dsstox-id nil="true"/>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>4-dimethoxyphosphinothioyloxy-3-methoxybenzonitrile</iupac>
  <moldb-polar-surface-area nil="true"/>
  <moldb-refractivity nil="true"/>
  <moldb-polarizability nil="true"/>
  <moldb-rotatable-bond-count nil="true"/>
  <moldb-acceptor-count nil="true"/>
  <moldb-donor-count nil="true"/>
  <moldb-pka-strongest-acidic nil="true"/>
  <moldb-pka-strongest-basic nil="true"/>
  <moldb-physiological-charge nil="true"/>
  <moldb-number-of-rings nil="true"/>
  <moldb-alogps-logp nil="true"/>
  <moldb-alogps-logs nil="true"/>
  <moldb-alogps-solubility nil="true"/>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organic acids and derivatives</superklass>
  <klass>Organic thiophosphoric acids and derivatives</klass>
  <subklass>Thiophosphoric acid esters</subklass>
  <paper-count type="integer" nil="true"/>
  <sync-id>CED0230117</sync-id>
  <structure-inchikey>JFEUEPKNHJHJDY-UHFFFAOYSA-N</structure-inchikey>
  <structure-fingerprint>40080000000000000000242000000000000000000000080000000000000400000000000004000000000040000000000000000000000000000000000000000000000000000000000000440000000000000000030000100000000000000000000000200000000000040000000100000000000000000000000000000000000000000000040000000000000000000800000000000000000000000000400000000000000000000000000000000088000000000000000000010000000000000000080000000000000000000000000000000000000000001000040000200000000000000000000000000000040000000000000000000200021000000000000000000</structure-fingerprint>
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  <structure-pickle>ï¾­Þ������������������������€���`�������(������@(������@(������@h�������@h�������@(������@h��������(�������(�������(������� ������(������� ������`������� ������`����������� ��h���h���h���h���h��� �	(��
 
������������������h�B���������������������</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T04:53:38Z</structure-indexed-at>
</compound>
