346366 <common-name>(2-hydroxy-3-phenoxypropyl)-triphenylphosphanium</common-name> <description>(2-hydroxy-3-phenoxypropyl)-triphenylphosphanium is a compound with the formula C27H26O2P+. It has an average molecular weight of 413.50 g/mol.</description> <cas nil="true"/> <pubchem-id>3692562</pubchem-id> <chemical-formula>C27H26O2P+</chemical-formula> <weight>413.5</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">2026-08-31T09:47:11Z</created-at> <updated-at type="dateTime">2026-08-31T09:47:11Z</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>C1=CC=C(C=C1)OCC(C[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)O</moldb-smiles> <moldb-formula>C27H26O2P+</moldb-formula> <moldb-inchi>InChI=1S/C27H26O2P/c28-23(21-29-24-13-5-1-6-14-24)22-30(25-15-7-2-8-16-25,26-17-9-3-10-18-26)27-19-11-4-12-20-27/h1-20,23,28H,21-22H2/q+1</moldb-inchi> <moldb-inchikey>CGRWJLBHCCIIGA-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">413.1670421</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>5.7</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id nil="true"/> <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>CHEM342259</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>(2-hydroxy-3-phenoxypropyl)-triphenylphosphanium</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>Benzenoids</superklass> <klass>Benzene and substituted derivatives</klass> <subklass>Phenylphosphines and derivatives</subklass> <paper-count type="integer" nil="true"/> <sync-id>CED0296719</sync-id> <structure-inchikey>CGRWJLBHCCIIGA-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>40000000000000000000800002000200000000000000000000000000100000000000000000000000200000000000000004000000000800000000000000000000000000000000200000000000000000000000200000800100000000000000000000000000010000000000000000000000000000000000000000000000000000000000000000040000800000000000010000000000000100000000000000000000000000000000000000000000080000000000000004080000000000000000000000000000000000000000000000002000000000000000000000000200000000000000000000020000000044000000000000000200000000000000000000000200</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAAeAAAAIQAAAIABBkBoAAAAAwMBBkBoAAAA AwMBBkBoAAAAAwMBBkAoAAAAAwQGQGgAAAADAwEGQGgAAAADAwEIACgAAAAD AgYAYAAAAAICBgBgAAAAAwEGAGAAAAACAg8gIgAAAAEEBkAoAAAAAwQGQGgA AAADAwEGQGgAAAADAwEGQGgAAAADAwEGQGgAAAADAwEGQGgAAAADAwEGQCgA AAADBAZAaAAAAAMDAQZAaAAAAAMDAQZAaAAAAAMDAQZAaAAAAAMDAQZAaAAA AAMDAQZAKAAAAAMEBkBoAAAAAwMBBkBoAAAAAwMBBkBoAAAAAwMBBkBoAAAA 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