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<compound>
  <id type="integer">102504</id>
  <title nil="true"/>
  <common-name>4-(1-Methyl-2-phenylethyl)-N-phenylaniline</common-name>
  <description>4-(1-Methyl-2-phenylethyl)-N-phenylaniline belongs to the stilbenes, a class of phenylpropanoids and polyketides within the organic compounds. This compound has the chemical formula C21H21N and an average molecular weight of 287.41 g/mol.</description>
  <cas>97375-16-1</cas>
  <pubchem-id>3024845</pubchem-id>
  <chemical-formula>C21H21N</chemical-formula>
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  <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">2026-04-05T09:35:11Z</created-at>
  <updated-at type="dateTime">2026-04-05T09:35:11Z</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>CC(CC1=CC=CC=C1)C1=CC=C(NC2=CC=CC=C2)C=C1</moldb-smiles>
  <moldb-formula>C21H21N</moldb-formula>
  <moldb-inchi>InChI=1/C21H21N/c1-17(16-18-8-4-2-5-9-18)19-12-14-21(15-13-19)22-20-10-6-3-7-11-20/h2-15,17,22H,16H2,1H3</moldb-inchi>
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  <moldb-average-mass type="decimal">287.406</moldb-average-mass>
  <moldb-mono-mass type="decimal">287.1673997</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp nil="true"/>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id 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>CHEM098397</chemdb-id>
  <dsstox-id>DTXSID90913958</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00065971</susdat-id>
  <iupac nil="true"/>
  <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>Phenylpropanoids and polyketides</superklass>
  <klass>Stilbenes</klass>
  <subklass nil="true"/>
  <paper-count type="integer">0</paper-count>
  <sync-id>CED0120737</sync-id>
  <structure-inchikey>KCCZEHRZIJVJCU-UHFFFAOYSA-N</structure-inchikey>
  <structure-fingerprint>40000000000000000001800000000000000000000000000100000000000000000000001000000000000000100000000004000000000000000400000000100200000000000000000000000000000000000000000000000001000000000000000000000000000000000010004000000000000000000000000000000000000000000000000040200000800000000000000080000000000100000000000000000000000000000000000000000400080000000000000000000000000000000000080000000000000000000040000000000000000000000000000000000220000000000000000000000804000040000000000000000000000000000000000000000000</structure-fingerprint>
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  <structure-indexed-at type="dateTime">2026-09-19T04:40:27Z</structure-indexed-at>
</compound>
