123488 <common-name>4-Amino-5,5,6,6,7,7,7-heptafluorohept-3-en-2-one</common-name> <description>4-Amino-5,5,6,6,7,7,7-heptafluorohept-3-en-2-one is an organic compound with the chemical formula C7H6F7NO and an average molecular weight of 253.12 g/mol. 4-Amino-5,5,6,6,7,7,7-heptafluorohept-3-en-2-one belongs to the carbonyl compounds, a subclass of organooxygen compounds within the organic compounds. This substance is found in or released from 13 recorded sources across multiple sectors. In electrical and electronic equipment, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. Within textiles, leather and furnishings, it is found in carpets, rugs, and synthetic textiles. It is also present in food packaging from the food, food processing and cookware sector, as well as medical devices from the healthcare, pharmaceuticals and veterinary products sector. Additionally, the compound is linked to lubricants used in both energy, oil and gas, as well as industrial manufacturing and chemical processing, along with one more sector. Recorded routes of exposure for this compound include inhalation, oral ingestion, and touch.</description> <cas>70168-24-0</cas> <pubchem-id>85443964</pubchem-id> <chemical-formula>C7H6F7NO</chemical-formula> <weight>253.12</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">2026-04-06T06:50:17Z</created-at> <updated-at type="dateTime">2026-08-24T05:10:24Z</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>CC(=O)C=C(N)C(F)(F)C(F)(F)C(F)(F)F</moldb-smiles> <moldb-formula>C7H6F7NO</moldb-formula> <moldb-inchi>InChI=1S/C7H6F7NO/c1-3(16)2-4(15)5(8,9)6(10,11)7(12,13)14/h2H,15H2,1H3</moldb-inchi> <moldb-inchikey>NZQRKNKAYBTPRP-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">253.12</moldb-average-mass> <moldb-mono-mass type="decimal">253.0337614</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>2.3</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>CHEM119381</chemdb-id> <dsstox-id>DTXSID70895622</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00111422</susdat-id> <iupac>4-Amino-5,5,6,6,7,7,7-heptafluorohept-3-en-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>Organic oxygen compounds</superklass> <klass>Organooxygen compounds</klass> <subklass>Carbonyl compounds</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0117052</sync-id> <structure-inchikey>NZQRKNKAYBTPRP-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100000000000042000000800000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000800000000000000000000000020000000000200000000000400000000000000010000000000000000000200000000000000000000000000000000400000000040000000000000008000000000001000000000000000200000000000000000000000000000000000000002000001000000040000000000004000000000000000000000000000000000002000000000000000000000000000000000000000000004000000000000000000000400800000000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAAQAAAADwAAAIABBgBgAAAAAQMGACgAAAAD BAgAKAAAAAMCBgBoAAAAAwMBBgAoAAAAAwQHAGgAAAADAQIGACAAAAAECQAg AAAAAQkAIAAAAAEGACAAAAAECQAgAAAAAQkAIAAAAAEGACAAAAAECQAgAAAA AQkAIAAAAAEJACAAAAABCwABAAECKAIBAyADBCgCBAUgBAYABgcABggABgkA CQoACQsACQwADA0ADA4ADA8AQgAAAAAXBAAAAAAAAAAW </structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:46:40Z</structure-indexed-at> </compound>