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<compound>
  <id type="integer">75756</id>
  <title nil="true"/>
  <common-name>6-Fluoro-1H-indole-3-ethylamine monohydrochloride</common-name>
  <description>6-Fluoro-1H-indole-3-ethylamine monohydrochloride belongs to the tryptamines and derivatives, a subclass of indoles and derivatives within the organic compounds. This organoheterocyclic compound has the chemical formula C10H11F1N2 and an average molecular weight of 214.67 g/mol. It has been found in or released from one recorded source: Electrical &amp; Electronic Equipment (Antennas).</description>
  <cas>55206-24-1</cas>
  <pubchem-id>74764475</pubchem-id>
  <chemical-formula>C10H11F1N2</chemical-formula>
  <weight>178.21</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">2026-04-04T05:05:07Z</created-at>
  <updated-at type="dateTime">2026-08-17T22:15:47Z</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>Cl.NCCC1=CNC2=C1C=CC(F)=C2</moldb-smiles>
  <moldb-formula>C10H11F1N2</moldb-formula>
  <moldb-inchi>InChI=1S/C10H11FN2/c11-8-1-2-9-7(3-4-12)6-13-10(9)5-8/h1-2,5-6,13H,3-4,12H2</moldb-inchi>
  <moldb-inchikey>ODVDIBHWTMTHOS-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">214.67</moldb-average-mass>
  <moldb-mono-mass type="decimal">178.090627</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp>1.9</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id>20714</chemspider-id>
  <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>CHEM071649</chemdb-id>
  <dsstox-id>DTXSID90203705</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00033263</susdat-id>
  <iupac>2-(6-fluoro-1H-indol-3-yl)ethanamine;hydron;chloride</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>Organoheterocyclic compounds</superklass>
  <klass>Indoles and derivatives</klass>
  <subklass>Tryptamines and derivatives</subklass>
  <paper-count type="integer">0</paper-count>
  <sync-id>CED0182974</sync-id>
  <structure-inchikey>ODVDIBHWTMTHOS-UHFFFAOYSA-N</structure-inchikey>
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  <structure-indexed-at type="dateTime">2026-09-19T04:23:57Z</structure-indexed-at>
</compound>
