304649 <common-name>3-(3,4-dichlorobenzoyl)-4-hydroxy-1h-quinolin-2-one</common-name> <description>3-(3,4-dichlorobenzoyl)-4-hydroxy-1h-quinolin-2-one belongs to the 4-aroylquinolines, a subclass of quinolines and derivatives within the organic compounds. This organoheterocyclic compound has the chemical formula C16H9Cl2NO3 and an average molecular weight of 334.10 g/mol.</description> <cas>90182-25-5</cas> <pubchem-id>135687103</pubchem-id> <chemical-formula>C16H9Cl2NO3</chemical-formula> <weight>334.1</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">2026-08-28T22:10:21Z</created-at> <updated-at type="dateTime">2026-08-28T22:10:21Z</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=C2C(=C1)C(=C(C(=O)N2)C(=O)C3=CC(=C(C=C3)Cl)Cl)O</moldb-smiles> <moldb-formula>C16H9Cl2NO3</moldb-formula> <moldb-inchi>InChI=1S/C16H9Cl2NO3/c17-10-6-5-8(7-11(10)18)14(20)13-15(21)9-3-1-2-4-12(9)19-16(13)22/h1-7H,(H2,19,21,22)</moldb-inchi> <moldb-inchikey>FAUSNNYBSWIXMI-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal" nil="true"/> <moldb-mono-mass type="decimal">332.9959485</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>4.1</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>CHEM300542</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>3-(3,4-dichlorobenzoyl)-4-hydroxy-1h-quinolin-2-one</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>Quinolines and derivatives</klass> <subklass>4-aroylquinolines</subklass> <paper-count type="integer" nil="true"/> <sync-id>CED0255777</sync-id> <structure-inchikey>FAUSNNYBSWIXMI-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>400000000000000000000000000100000000000000000000200000000000000000000000000020000000100002000000000000000000000000000000000000000000000000400000202000000000000020002000000000800000000012000000000000010000000000000000100000000000000000000000000000010000000000000001000000800000200000000000000000000100000000000000000000000010000000000000040000084000200000000000000000000000000000000000002000040000002000000000000000000010004000000000004200000001000000000000000002000040000000000400000000000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ������������������������€��@h�������@h�������@h�������@(������@(������@h�������@(������@(������@(�������(������@8��������(�������(������@(������@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">2026-09-19T05:13:36Z</structure-indexed-at> </compound>