124001 <common-name>3-Chloro-5-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)pyridin-2(1H)-one</common-name> <description>3-Chloro-5-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)pyridin-2(1H)-one belongs to the hydropyridines, a subclass of pyridines and derivatives within the organic compounds. This organoheterocyclic compound has the chemical formula C8H3ClF7NO and an average molecular weight of 297.56 g/mol. The compound is found in or released from 13 recorded sources across several sectors. In the electrical and electronic equipment sector, it is associated with capacitors, cell phones, batteries, wires and cables, printed circuit boards, and one additional source. Within the textiles, leather and furnishings sector, it is found in carpets, rugs, and synthetic textiles. Other recorded sources include medical devices from the healthcare, pharmaceuticals and veterinary products sector, food packaging from the food, food processing and cookware sector, and lubricants from both the energy, oil and gas sector and the industrial manufacturing and chemical processing sector, as well as one further sector. Recorded exposure routes for this substance include touch, oral, and inhalation.</description> <cas>1771743-43-1</cas> <pubchem-id>118065026</pubchem-id> <chemical-formula>C8H3ClF7NO</chemical-formula> <weight>297.56</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">2026-04-06T07:25:41Z</created-at> <updated-at type="dateTime">2026-09-01T13:34:00Z</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>FC(F)(F)C(F)(C1=CNC(=O)C(Cl)=C1)C(F)(F)F</moldb-smiles> <moldb-formula>C8H3ClF7NO</moldb-formula> <moldb-inchi>InChI=1S/C8H3ClF7NO/c9-4-1-3(2-17-5(4)18)6(10,7(11,12)13)8(14,15)16/h1-2H,(H,17,18)</moldb-inchi> <moldb-inchikey>YXTGUYDNPREZFO-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">297.56</moldb-average-mass> <moldb-mono-mass type="decimal">296.9791389</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>2.8</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>CHEM119894</chemdb-id> <dsstox-id>DTXSID90896378</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00112167</susdat-id> <iupac>3-Chloro-5-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)pyridin-2(1H)-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>Pyridines and derivatives</klass> <subklass>Hydropyridines</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0117541</sync-id> <structure-inchikey>YXTGUYDNPREZFO-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100000000000102100000000000000000200000008000000080000000000000020000000000002001000000080000000000000000000000000000000000000400000000000000000000020000000000000000000000002000800000000020000000000000000100000000000000000000000000000000000000000000000000000000010200000000000000000000000000000000000000000000000000000000000000000080000000040000000040000000000000000000000000000000000000000000000000000000010000000000000000000000000000000000000000000000041000000000000800000000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAASAAAAEgAAAIABCQAgAAAAAQYAIAAAAAQJ ACAAAAABCQAgAAAAAQYAIAAAAAQJACAAAAABBkAoAAAAAwQGQGgAAAADAwEH QDgAAAADAQMGQCgAAAADBAgAKAAAAAMCBkAoAAAAAwQRACAAAAABBkBoAAAA AwMBBgAgAAAABAkAIAAAAAEJACAAAAABCQAgAAAAAQsAAQABAgABAwABBAAE BQAEBgAGB2gMBwhoDAgJaAwJCigCCQtoDAsMAAsNaAwEDgAODwAOEAAOEQAN BmgMQgEAAAAGBg0LCQgHFwQAAAAAAAAAFg== </structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:47:03Z</structure-indexed-at> </compound>