123495 <common-name>N-(2,2,3,3,4,4,4-Heptafluorobutyl)prop-2-enamide</common-name> <description>N-(2,2,3,3,4,4,4-Heptafluorobutyl)prop-2-enamide is an organic compound with the chemical formula C7H6F7NO and an average molecular weight of 253.12 g/mol. N-(2,2,3,3,4,4,4-Heptafluorobutyl)prop-2-enamide belongs to the acrylic acids and derivatives, a subclass of carboxylic acids and derivatives within the organic compounds. This substance is associated with 13 recorded sources across multiple sectors. In the electrical and electronic equipment sector, it is found in cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. It is present in textiles, leather and furnishings, specifically within carpets, rugs, and synthetic textiles. Other sources include 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 found in lubricants used in energy, oil and gas, as well as industrial manufacturing and chemical processing, along with one other sector. Recorded exposure routes for this compound include inhalation, oral, and touch.</description> <cas>1422-65-7</cas> <pubchem-id>2774882</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">2026-04-06T06:50:34Z</created-at> <updated-at type="dateTime">2026-08-24T05:10:20Z</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)(F)C(F)(F)CNC(=O)C=C</moldb-smiles> <moldb-formula>C7H6F7NO</moldb-formula> <moldb-inchi>InChI=1S/C7H6F7NO/c1-2-4(16)15-3-5(8,9)6(10,11)7(12,13)14/h2H,1,3H2,(H,15,16)</moldb-inchi> <moldb-inchikey>SQBHHHGUOQBSBF-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>2.6</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>CHEM119388</chemdb-id> <dsstox-id>DTXSID70895687</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00111429</susdat-id> <iupac>N-(2,2,3,3,4,4,4-Heptafluorobutyl)prop-2-enamide</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 acids and derivatives</superklass> <klass>Carboxylic acids and derivatives</klass> <subklass>Acrylic acids and derivatives</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0120391</sync-id> <structure-inchikey>SQBHHHGUOQBSBF-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>100000800000002000000000000000000004000000000000000000000000000000010000000000000000000000000000000000000000000000000000800000000010000000000000000020000000000200000000000000000000000000010000000000000000000200000000000000000100000000000040000000000800000000000000000000000080000004000000000000000000000000000000000000000000000200000002000000000000040000000000800200000000000000000000000000000000040000000000000000000000000000000000000400000000000000000000000000000400800000000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ������������������������€� � ������ ���� � ���� � ������ ���� � ���� � ������ ���� � ���� � ������`�������h��������(�������(�������h��������h�������������������������������� �� � ���� � (��� ��(�B��������������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:46:40Z</structure-indexed-at> </compound>