76381 <common-name>N-(3-Hydroxyphenyl)benzenesulphonamide</common-name> <description>N-(3-Hydroxyphenyl)benzenesulphonamide belongs to the sulfanilides, a subclass of benzene and substituted derivatives within the organic compounds. It is a member of the benzenoids superclass with the formula C12H11N1O3S1. The compound has an average molecular weight of 249.28 g/mol.</description> <cas>59149-19-8</cas> <pubchem-id>97359</pubchem-id> <chemical-formula>C12H11N1O3S1</chemical-formula> <weight>249.29</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">2026-04-04T06:26:49Z</created-at> <updated-at type="dateTime">2026-08-18T16:11:02Z</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>OC1=CC=CC(NS(=O)(=O)C2=CC=CC=C2)=C1</moldb-smiles> <moldb-formula>C12H11N1O3S1</moldb-formula> <moldb-inchi>InChI=1S/C12H11NO3S/c14-11-6-4-5-10(9-11)13-17(15,16)12-7-2-1-3-8-12/h1-9,13-14H</moldb-inchi> <moldb-inchikey>JKQZPAGBJKFTQC-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">249.28</moldb-average-mass> <moldb-mono-mass type="decimal">249.045964</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>2.2</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>87877</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>CHEM072274</chemdb-id> <dsstox-id>DTXSID70207882</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00034097</susdat-id> <iupac>N-(3-hydroxyphenyl)benzenesulfonamide</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>Sulfanilides</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0115284</sync-id> <structure-inchikey>JKQZPAGBJKFTQC-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>80000000000000040000000000000000000000000000001000000000000000004000000000000010000000200000004040000000000000000000000000002000000000000000001000000000000000000200000000000010000000001c0000000000000010000000000000000101000000000000000000000000000000000000001000000000000800000000000000080000000000100000000000000000200000000000000000000000000080000000000000000000000080000000000000000000000000000002000000000000000000000000000000000000200000000000000000000000000000040000000000000000000000000000000000000000000</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">2026-09-19T04:24:24Z</structure-indexed-at> </compound>