286714 <common-name>1-(4-chlorophenyl)-3-(3-hydroxyphenyl)urea</common-name> <description>1-(4-chlorophenyl)-3-(3-hydroxyphenyl)urea belongs to the n-phenylureas, a subclass of benzene and substituted derivatives within the organic compounds. This benzenoid compound has the chemical formula C13H11ClN2O2 and an average molecular weight of 262.69 g/mol.</description> <cas>303092-13-9</cas> <pubchem-id>5159568</pubchem-id> <chemical-formula>C13H11ClN2O2</chemical-formula> <weight>262.69</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">2026-08-27T22:58:54Z</created-at> <updated-at type="dateTime">2026-08-27T22:58:54Z</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(=CC(=C1)O)NC(=O)NC2=CC=C(C=C2)Cl</moldb-smiles> <moldb-formula>C13H11ClN2O2</moldb-formula> <moldb-inchi>InChI=1S/C13H11ClN2O2/c14-9-4-6-10(7-5-9)15-13(18)16-11-2-1-3-12(17)8-11/h1-8,17H,(H2,15,16,18)</moldb-inchi> <moldb-inchikey>MUXHPBRGFKUQDV-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">262.0509053</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>2.7</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>CHEM282607</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>1-(4-chlorophenyl)-3-(3-hydroxyphenyl)urea</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>N-phenylureas</subklass> <paper-count type="integer">80</paper-count> <sync-id>CED0020461</sync-id> <structure-inchikey>MUXHPBRGFKUQDV-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>804000000000000000000000000000008100000080000000000400000000000000000000000000000400000000000000000000000000000000000000000000400000000000000000000020000000000001000000000040000000000000010080000010000000100000000000000000000000000000000000000001000000020400800000000000000080000000000000000000000000000000000000000000000000000000080000000000000000000000000000000000000000000000000000002000000000000000000010000000000000000200000000000000008000000000000040000000000400000000000000000600000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ������������������������€��@h�������@h�������@(������@h�������@(������@h��������h��������h��������(�������(�������h�������@(������@h�������@h�������@(������@h�������@h�������� �������h���h���h���h���h��� �� �� � (�� � ��h�� h� �h���h���h������h���h�B������������� ��������������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T05:00:17Z</structure-indexed-at> </compound>