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<compound>
  <id type="integer">98443</id>
  <title nil="true"/>
  <common-name>Dihydro-2,2-dimethyl-6H-1,3,2-oxathiastannin-6-one</common-name>
  <description>Dihydro-2,2-dimethyl-6H-1,3,2-oxathiastannin-6-one belongs to the carboxylic acid derivatives, a subclass of carboxylic acids and derivatives within the organic compounds. This compound has the chemical formula C5H10O2SSn and an average molecular weight of 252.90 g/mol.</description>
  <cas>32673-05-5</cas>
  <pubchem-id>16684207</pubchem-id>
  <chemical-formula>C5H10O2SSn</chemical-formula>
  <weight>252.91</weight>
  <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">2026-04-05T06:06:11Z</created-at>
  <updated-at type="dateTime">2026-08-22T13:28:25Z</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>C[Sn]1(C)OC(=O)CCS1</moldb-smiles>
  <moldb-formula>C5H10O2SSn</moldb-formula>
  <moldb-inchi>InChI=1/C3H6O2S.2CH3.Sn/c4-3(5)1-2-6;;;/h6H,1-2H2,(H,4,5);2*1H3;/q;;;+2/p-2/rC5H10O2SSn/c1-9(2)7-5(6)3-4-8-9/h3-4H2,1-2H3</moldb-inchi>
  <moldb-inchikey>YZWBIXWWOWRJCW-UHFFFAOYSA-L</moldb-inchikey>
  <moldb-average-mass type="decimal">252.9</moldb-average-mass>
  <moldb-mono-mass type="decimal">253.9423453</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp nil="true"/>
  <hmdb-id nil="true"/>
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  <chemspider-id nil="true"/>
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  <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>CHEM094336</chemdb-id>
  <dsstox-id>DTXSID1067708</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00060990</susdat-id>
  <iupac>2,2-dimethyl-1,3,2-oxathiastanninan-6-one</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>Carboxylic acids and derivatives</klass>
  <subklass>Carboxylic acid derivatives</subklass>
  <paper-count type="integer">0</paper-count>
  <sync-id>CED0137214</sync-id>
  <structure-inchikey>YZWBIXWWOWRJCW-UHFFFAOYSA-L</structure-inchikey>
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  <structure-indexed-at type="dateTime">2026-09-19T04:38:12Z</structure-indexed-at>
</compound>
